Open Access

Comprehensive analysis of drugs to treat SARS‑CoV‑2 infection: Mechanistic insights into current COVID‑19 therapies (Review)

  • Authors:
    • George Mihai Nitulescu
    • Horia Paunescu
    • Sterghios A. Moschos
    • Dimitrios Petrakis
    • Georgiana Nitulescu
    • George Nicolae Daniel Ion
    • Demetrios A. Spandidos
    • Taxiarchis Konstantinos Nikolouzakis
    • Nikolaos Drakoulis
    • Aristidis Tsatsakis
  • View Affiliations

  • Published online on: May 18, 2020
  • Pages: 467-488
  • Copyright: © Nitulescu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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The major impact produced by the severe acute respiratory syndrome coronavirus 2 (SARS‑CoV‑2) focused many researchers attention to find treatments that can suppress transmission or ameliorate the disease. Despite the very fast and large flow of scientific data on possible treatment solutions, none have yet demonstrated unequivocal clinical utility against coronavirus disease 2019 (COVID‑19). This work represents an exhaustive and critical review of all available data on potential treatments for COVID‑19, highlighting their mechanistic characteristics and the strategy development rationale. Drug repurposing, also known as drug repositioning, and target based methods are the most used strategies to advance therapeutic solutions into clinical practice. Current in silico, in vitro and in vivo evidence regarding proposed treatments are summarized providing strong support for future research efforts.

1. Introduction

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), provisionally named as 2019-nCoV and colloquially known as the coronavirus, is the pandemic-causing pathogen behind coronavirus disease 2019 (COVID-19), which originated in Wuhan, Hubei Province, China in the 4th quarter of 2019 (1). Despite the rapid delivery of the SARS-CoV-2 genome by the group originally recognizing this novel viral pneumonia and the subsequent production of a number of highly specific and sensitive molecular diagnostics for SARS-CoV-2, progress in fighting this disease is balanced by the continued lack of ′quick win′ treatments that can suppress transmission or ameliorate disease. Of the more than 100 clinical trials evaluating a cadre of approved, or clinical stage antivirals and related compounds, none have yet demonstrated unequivocal clinical utility against COVID-19.

The eventual containment and mitigation of this emerging disease will depend on our exponentially increasing knowledge around SARS-CoV-2 virology, pathology, and cross-species transmission. With viral genome organization resolved in unprecedented speed, molecular pathogenesis and immunopathology related to protein products, modes of transmission, host cell entry mechanism and kinetics, vesicular trafficking, protein and small molecule interaction, biological and replication machinery mechanisms of action, are only beginning to be understood. Likewise, the propensity for deleterious inflammatory responses is episodically studied against SARS-CoV-2 antigen presentation, antigen-specific antibody and cell mediated responses contributing to protective adaptive immunity and the attenuation of disease severity, as well as pulmonary and systemic tissue destruction. Comprehensive interrogation of the viral-human interactome, and associated chemoinformatic analyses (2,3) nevertheless offer hope for the identification of nodal intervention points across the continuum of COVID-19 disease (4,5). As elucidation of these phenomena will undoubtedly incur delays in developing appropriate pharmacological interventions, clinical attention is understandably focused on US Food and Drug Administration (FDA) approved drugs which present putative treatments aligned to our present under-standing of SARS-CoV (the agent of 2002-2003 Guangdong Corinavirus epidemic) and Middle East respiratory syndrome virus (MERS-CoV) infections, followed by compounds in clinical, or even late pre-clinical investigation (6,7).

2. Virological, genomic, and host aspects related to COVID-19 treatment

SARS-CoV-2 is a pleomorphic, enveloped, positive-sense single-stranded RNA virus [(+)ssRNA] which encodes 15 or 16 replicate-related proteins, 4 or 5 structural proteins and 1-8 group-specific or accessory proteins from the Orthocoronavirinae subfamily, Coronaviridae family, order Nidovirales (8). Coronaviridae are a large family that includes at least four viruses responsible for common colds: four human coronaviruses (HCoV 229E, NL63, OC43, and HKU1) account for up to a third of adult upper respiratory tract infections (9). A phylogenetic tree of alpha-beta coronavirus is presented in Fig. 1.

SARS-CoV-2 shows great phylogenetic similarity to several strains of coronavirus isolated from bats in China, sharing 88% identity with bat-SL-CoVZC45 and bat-SL-CoVZXC21 which were isolated in Zhoushan, eastern China (10), more than 96% genomic similarity with BatCoV RaTG13 collected in Yunnan Province (11), and to a lesser extent to SARS-CoV (approximately 79% homology). By contrast, the camelid-originating MERS-CoV shares approximately 50% homology to SARS-CoV-2 (10).

Measuring a sizeable 29.8 kb, the SARS-CoV-2 genome is flanked by short 5′ and 3′ highly structured untranslated regions (UTRs) commonplace in RNA viruses and contains at least 14 open reading frames (ORFs) encoding 27 proteins organized in a manner typical of other coronaviruses (CoVs) (12) (Fig. 2). The first ORFs are translated into two large polyproteins (pp1a and pp1ab) cytosolically processed into the non-structural proteins (nsp) 1-16. These contain the polyprotein-processing protease nsp5, a host RNA restriction factor (nsp1) arresting canonical translation, and collectively function as the viral replicase-transcriptase complex (2) by rearranging rough endoplasmic reticulum (RER) membranes into double-membrane vesicles (DMVs) wherein replication, transcription and virion assembly take place (13,14). The immunomodulatory protein nsp16 is 2′-O-ribose methyl transferase that renders the virus a toll-like receptor (TLR) 7/8 antagonist (15) and is believed to enhance the purported capacity of the virus to evade antiviral interferon-generating cytosolic pathogen associated molecular pattern recognition receptors, such as the double stranded RNA (dsRNA) sensing protein kinase R (PKR) and TLR3, on account of the DMV replication organelle structure (16). An additional protein of key pharmacological interest the RNA-dependent RNA polymerase (RdRp) nsp12, which is the primary target of the so-called directly acting antiviral (DAA) drug family. The remaining ORFs encode the so-called spike (S or SARS-2-S) protein responsible for virus tropism, as well as envelope I, nucleocapsid (N) and membrane (M) structural proteins. The mechanistic role of many of the remaining accessory proteins that are redundant to viral replication remains undetermined (7).

The human angiotensin-converting enzyme 2 (ACE2) cell surface recaptor has been confirmed as the primary cell attachment factor for SARS-CoV-2 (18). This single transmembrane domain protein is expressed at appreciable protein levels on terminal bronchiole as well as type I and II lung alveolar epithelium cells, which aligns with the primary pathology of COVID-19: loss of O2 saturation due to poor pulmonary gas exchange. Likewise, noteworthy ACE2 levels have been reported among enterocytes of the small intestine, arterial, and venous endothelial cells, and arterial smooth muscle cells in most organs, as well as the vagus nerve innervating the lung, heart and digestive system (19,20), which mirror the diversity of symptoms and pathologies associated with COVID-19: diarrhea, myocarditis, fatigue, encephalopathy (headaches, confusion, anosmia, stroke-like symptoms, and seizures). Following cellular attachment, pivotal to cellular entry is the type II transmembrane protease serine 2 (TMPRSS2) which process the SARS-CoV-2-S to expose a cell-membrane fusion peptide (21). Once membrane fusion is achieved, viral RNA is released into the infected host cell to initiate pathogenic responses and viral replication. In a first step, the open reading frame 1a/b (ORF1a/b) of the viral genome is translated to produce the replicate proteins, after which the replicase-transcriptase complex DMVs are assembled. In a second step, the replication complex reverse-transcribes the positive RNA genome into full-length negative-sense RNAs, which in turn template the production of daughter full-length genomes, and a subset of translation-focused mRNAs. These translation-dedicated transcripts contain a common 5′ leader sequence cytosolically spliced to downstream genes, which are added by discontinuous synthesis of minus sense subgenomic RNAs templating the positive RNA genome (22).

The genetic variance of SARS-CoV-2 is relatively small compared to other RNA viruses (23), since CoVs possess mechanisms of transcription error correction through the proofreading function of nsp14 (24), a protein common to MERS-CoV and SARS-CoV, which renders them collectively immune to ribavirin (25), but is also reported to drive recombinatory promiscuity (24). Consequently, ciral quasi-species are relatively suppressed within patients, and mutation primarily leads to single nucleotide polymorphisms (SNPs). Nearly 200 such mutations have been reported as of mid-April 2020 (26). Based on the analysis of more than 100 virus isolates, two main genetic variants of SARS-CoV-2 were initially identified, which are referred to by some members of the community as L-type and S-type, differing only by 2 SNPs. The L-type probably evolved from the S-type and is the more widespread and ′aggressive′ variant (27). Another study with 160 virus isolates from different countries classified the virus into A, B and C type, the type A being the oldest virus variant. Types A and C are most common in Europe and America, while type B predominates in Asia (26). More recently, controversy over the transmission propensity of the so-called L-type variant, which harbours the noteworthy D614G mutation on SARS-CoV-2-S (28), has been ascribed to mutation recurrence and multiple geographical introductions as elucidated through the analysis of 7,666 published SARS-CoV-2 genomes (29). However, the impact of these mutations, particularly on protein core to the virus replication cycle such as the cell tropism- and attachment affinity-defining SARS-CoV-2-S remains experimentally undetermined.

The current consensus among the scientific community remains that the main sites of SARS-CoV-2 infection and replication are both the upper and lower respiratory tracts, despite viral loads being consistenly higher, and more reliable to detect in lower respiratory tract speciments. However, this position, largely driven by RT-PCR detection of SARS-CoV-2 and therefore, by extrapolation replication, does not align with the near dearth of ACE2 expression in the upper respiratory tract and oral mucosa (20). The only exceptions to these data are recent reports of olfactory epithelium ACE2 expression in mice (30) which is in line with anosmic symptomatology in man, and early evidence of interferon-induced increase in ACE2 expression in upper respiratory tract sites, which would be secondary to infection and replication in either distal, or physiologically non-epithelial local cell types (31). Curiously, endothelial ACE2 expression appears to be ubiquitous even in the upper respiratory tract (20). These findings postulate three hypotheses on the infection and replication cascade of SARS-CoV-2. The simplest of these assumes direct infection of upper respiratory tract epithelia from fomites or large droplets (cough), followed by progressing infection to the lower lung by week 2, which would explain deteriorating clinical image in cases requiring hospitalization. However, this hypothesis would rely on transcytotic epithelial mechanisms delivering SARS-CoV-2 to ACE2-expressing basal upper respiratory/oral epithelial cells or endothelia (20). Though transcytotic mechanisms are not implausible (32,33), these cells would in turn propagate the virus locally, causing interferon-induced ACE2 epithelial overexpression, epithelial cell infection, and luminal virus shedding, ultimately leading to the observations of low-level detection in nasopharyngeal and oropharyngeal swabs by RT-PCR. However, the immunomodulatory capacity of SARS-CoV-2 manifest through DMVs and nsp16 (13,14,16), in addition to the consistently higher viral load in the lower respiratory tract as opposed to the relatively virus-free upper respiratory tract strongly disfavour this hypothesis. The second hypothesis would require direct infection of the olfactory epithelium again by fomites or droplets, local replication and retrograde transport to the lower lung, whereupon the virus would establish disease-causing replication. However, the infrequent incidence of anosmia coupled to the opposite direction of travel for tracheobronchial mucocilliary clearance, and the need for sub-3 micron aerosol particle dimensions to access the alveoli that would have to be generated in the nose, present a formidable set of physiological barriers to the virus for accessing the lower lung. The last hypothesis would require direct infection of the lower respiratory tract through inhalation of SARS-CoV-2 containing aerosols, directly infecting the ACE2-overexpressing alveoli, sequentially driving upper respiratory tract infection through mucocilliary clearance and aerosol generation in exhaled breath. Poignantly, this putative infection progression sequence aligns with ACE2 protein expression data, SARS-CoV-2 levels reported by RT-PCR across the respiratory tracts of patients, and offers a mechanistic explanation for the rarity of anosmia and low nasopharyngeal carriage of the virus, as diminishing quantities of aerosolized virus would need to diffuse into the mucous found in these tissues upon exhalation. Critically, data documenting viral particle production in upper respiratory tract (or oral) epithelial or indeed endothelial cells remain elusive from both human and animal studies.

3. Pathogenesis

Even though the replication site of the virus is admittedly the lower respiratory system the virus can affect the function of secondary organs that also express ACE2, such as the kidney, GI tract, liver, and gall bladder. Typically, this results in symptom severity that drives patients to seek medical attention, usually by week 2 after symptom onset. However, to date no single clincal report has documented measurable, or at least appreaciable amounts of virus in the peripheral blood of patients admitted with COVID-19. One possible explanation of the practically undetectable levels of SARS-CoV-2 in blood might be the arrival time of patients to hospitals (week 2), by which time seroconversion and neutralizing antibodies are being generated and thus viraemia suppressed. Alternatively, endothelial ACE2 expression reduces blood viral load below the limit of detection of RT-PCR (~15,000 copies/ml whole blood) by sequestering free viral particles from suspension. However, such extent of ACE2 expression systemically across endothelia is not corroborated in public protein expression data repositories (e.g.,, nor is it physiologically evidenced by the loss of endothelial barrier function as is common in haemorrhagic fever viral infections. Taken together, these findings cast doubts on hypotheses regarding the mechanism of transfer of SARS-CoV-2 from the respira-tory tract to the intestines (34), which is manifested through faecal detection of SARS-CoV-2 RNA (35) and protein in lower GI tract (36). By stark contrast, the main sites of ACE2 expression, i.e., the lung, GI tract, kidneys, liver and gall-bladder, and indeed the testis in men, wherein SARS-CoV-2 replication has also been documented (37), are all innervated by the vagus nerve.

The median time from symptom onset to acute respiratory distress syndrome, the principal reason for COVID-19 patients seeking medical attention, is approximately 8 days; around this timepoint COVID-19 appears to morph from an acute viral infection to what might appear to be a second attack, causing the patient′s condition to worsen over the second week after symptom onset. Critically, continued deterioration beyond day 14 is associated with high mortality. Thus the disease could be divided into three major stages after symptom onset: in the first stage symptomatic patients report initially mild-to-moderate, but quality of life impacting non-specific symptoms (days 0-7) associated with a progressive drop in viral load; stage II, wherein severe dyspnoea and associated pneumonia drive patients to seek medical attention; and, finally stage III, a severe respiratory symptomatic stage potentially with high viral load, but most commonly characterised by runaway inflammatory responses associated with multiple organ failure (38,39).

Thus, the ensuing innate immune response might be two-phased; instead of the early innate immunity containing the virus towards the developement of adaptive immunity, in some patients there would appear to be a loss of key checkpoint functions driving a secondary, damaging inflammatory phase. The second inflammatory phase is driven by the cytokine release syndrome (the so-called ′cytokine storm′) and affects patients with severe conditions. Although genetic differences may underpin innate response amplitude between individuals, viral amplification appears to ensue (40) causing direct or, more likely, indirect destruction of tissues affected by the so-called ′happy hypoxia′ associated with COVID-19, the otherwise asymptomatic critical reduction of blood oxygen saturation below 95%, sometimes reportedly as low as 50%, i.e., well below the level normally associated with respiratory arrest.

The early antibody response against SARS-CoV-2 including IgA, IgM, and IgG response was examined by using an ELISA-based assay on the recombinant SARS-CoV-2 protein against the recombinant proteins for the other four common cold-causing human coronaviruses. The median time to IgM and IgA antibody detection was 5 days with interquartile range (IQR) 3-6, while IgG was detected on 14 days (IQR 10-18) after symptom onset, with a positive rate of 85.4, 92.7 and 77.9%, respectively (41). In a study of 23 patients with COVID-19, viral load was reported to be declining across the first week of illness, dropping below detection limits amongst most patients by week 2. With analytical sensitivity lacking between days 7-10, IgG and IgM antibodies were detectable more reliably at approximately 10 days after symptom onset, with most patients seroconverting within the first 3 weeks. Importantly, both IgG and IgM were observed to neutralize SARS-CoV-2-N and the recaptor binding domain of SARS-CoV-2-S (42).

Research data on late humoral response and persistence of neutralizing antibodies in SARS-CoV-2 infection is still limited. A major cause for concern are reports in China, Japan and South Korea of patients testing still positive by RT-PCR days, or even weeks after clinical discharge presumably on the basis of two consecutive negative RT-PCR results. Some patientsa are even reported to relapse, indicating that a sustained immune response may be difficult to obtain, or that at least humoral immunity is inadequate for infection elimination (40). Although the World Health Organization (WHO) has recently pronounced these observations as a consequence of RNA shedding from infected apoptotic epithelia in the respiratory tract, corroborating data in the literature are lacking. On the other hand, patients who have recovered from SARS-CoV have been reported to harbour potent antibody responses to SARS-S protein and its receptor binding domain (RBD) for at least three years, indicating that RBD-targeting vaccines under development might be adequately protective against COVID-19 (43,44).

Another aspect meriting attention is the progressive lymphopenia documented during COVID-19, which is principally manifest and most pronounced in severe cases, affecting CD4+ and CD8+ T cell levels, as well as B lymphocyte concentration, potentially adversely affecting antibody production. Thus, T cell lymphopenia and associated cytokine concentrations have been proposed as biomarkers of poor prognosis, with interleukin (IL)-6, IL-10, and D-dimer continued elevation marking transition to a severe disease state between days 7-14 after symptom onset, followed by further elevation of D-dimer, neutrophilia, blood urea nitrogen, and creatinine marking in the later, irreversible stages of disease. In contrast, IL-8 and tumor necrosis factor alpha (TNF-α) elevation appears to be associated and indeed peak early during the recovery phase (45,46).

4. Treatment strategies

In the absence of a clinically proven treatment for COVID-19, frontline clinicians are restricted to offering supportive symptomatic treatment such as oxygen therapy, steroids on a per case basis, fluid management, and broad-spectrum antibiotics against co- or secondary bacterial infections (45). Beyond these, as with any viral disease, therapeutic intervention may extend to either direct acting antivirals (DAAs) or immunomodulatory adjuvants and substances (47). Considering the drug discovery process, research efforts can be grouped in three major classifications. The first relies on the repurposing of approved, broad-spectrum antiviral drugs, through clinical trial and error. The major advantage of this approach consists of the clear knowledge about the drugs′ metabolic profile, dosages needed and supported, potential side effects, and risks. The disadvantage of these types of drugs is represented by their low selectivity and, often, poor utility between virus families. The second strategy is based on high-throughput screening, in silico, in cellulo or, more recently, by means of artificial intelligence drug discovery, to identify approved, or, at best, late stage drugs with promising therapeutical effects either through their intended mode of action (e.g., RNA dependent RNA polymerase inhibition), or through their well-described off-target effects (similar to kinase inhibitor promiscuity). The third strategy involves identifying the molecular and pathological characteristics of the disease in question, to develop entirely novel drugs that may target them. The advantage here would be the high selectivity and potentially high efficacy (48). Thankfully, the 18 years of head start knowledge gained against SARS-CoV-2 on the back of the SARS-CoV and MERS-CoV outbreaks of the early 21st century, have resulted in an unprecedented speed by which the molecular mechanisms of SARS-CoV-2 infection are being elucidated, not least because of the rapid elucidation of the genomic organization of SARS-CoV-2. These datasets have informed several rational, high confidence potential therapeutic targets against SARS-CoV-2 (10,49) (Fig. 3).

As the development of new drugs is a long and costly process, the urgency of the pandemic targeted early efforts on identifying candidate treatments among marketed drugs or approved, but later abandoned compounds. Drug repurposing, also known as drug repositioning, is one of the best solutions to identify therapeutic solutions for COVID-19 in a time-critical fashion (50).

Blocking virus cell entry. Penetration of host cells is an obligatory step in the life of any virus rendering it a powerful target for drug development (51). The discovery of the intrinsic mechanism of SARS-CoV-2-S to mediate cell entry focused efforts on ACE2 and the whole renin-angiotensin-aldosterone system (RAAS) (18,51). ACE2 is monocarboxypeptidase that hydrolyzes the bond between the carboxyl-terminal phenylalanine and proline in angiotensin II (Ang1-8) generating Ang1-7, a physiological antagonist of Ang1-8 with vasodilator and anti-inflammatory properties (52). Considering these effects, a soluble recombinant human ACE2 (rhACE2) was developed under the name APN01 (known also as GSK2586881) and evaluated in patients with pulmonary arterial hypertension (53) and acute pulmonary injury (54). In healthy volunteers rhACE2 was administered intravenously in doses from 100 to 1,200 µg/kg and was generally well-tolerated, with no significant effect on blood pressure and heart rate, and with only mild or moderate adverse events reported (52).

SARS-CoV-2-S engages ACE2 as the entry receptor in a similar way as the homologous SARS-CoV spike protein. The expression and distribution of the ACE2 on alveolar epithelial cells is consistent with the dry cough and dyspnea experienced by the patients. Consequently, it is anticipated that rhACE2 may act as a competitive interceptor of SARS-CoV-2 thereby reducing cell penetration and offering protection against infection (55). A randomized placebo-controlled study (NCT04335136) is scheduled to test rhACE2 in SARS-CoV-2 patients (56). Furthermore, several peptide derivatives of ACE2 were designed using molecular dynamics simulations as potential decoys that could be used as future inhaled therapeutics (57). However, drug development history (inhaled insulin, Exubera) denotes the brief residence time of soluble proteins in the respiratory lumen, necessitating modifications (58) that would sustain rhACE2 decoy potency at the primary infection site of interest for SARS-CoV-2, the respiratory epithelium.

Another strategy focused on ACE2 is based on the hypothesis that ACE2 activity is reduced by SARS-CoV-2-S, exposing the organism to higher levels of Ang1-8 which increases alveolar permeability and causes lung injury (59). Two compounds, resorcinolnaphthalein and 1-[(2-dimethylamino)ethylamino]-4-(hydro xymethyl)-7-[(4-methylphenyl)sulfonyloxy]-9H-xanthene-9-one, were identified in a large docking study as ACE2 activators and were demonstrated to enhance ACE2 activity in a dose-depen-dent manner, albeit with half-maximal effective concentration (EC50) values of 19.5±0.4 and 20.1±0.8 µM, respectively (60). Diminazene aceturate is a veterinary-approved antitrypanosomal drug that similarly activates ACE2 at comparable in vitro EC50, rendering protective effects in cardiovascular and type 1 diabetes experimental models (61,62). A recent review study presents the toxic effect of diminazene aceturate on the nervous system of some animals, but provides evidence that it was safe in thousands of trypanosomiasis patients from Uganda (62). These compounds could be a potential therapy in patients with SARS-CoV-2, provided topical dosing and pharmacology afford adequate activation of respiratory ACE2.

Likewise, use of Ang1-8 receptor 1 (AT1) antagonists to reduce the aggressiveness and mortality of SARS-CoV-2 infection based on two mechanisms, the blockade of the effects of excess Ang1-8, and the upregulation of ACE2 (63). Several clinical studies are underway to asses various AT1 antagonists: losartan 25 mg once daily (NCT04335123, NCT04328012, and NCT04311177) or 50 mg daily (NCT04312009), losartan 100 mg once daily alone or in combination with aspirin 150 mg once daily or simvastatin 80 mg once daily in an eight arms factorial trial (NCT04343001), telmisartan 80 mg twice daily (NCT04355936), valsartan 80 mg up to 160 mg (NCT04335786) (56).

Camostat is an orally active serine protease inhibitor of trypsin and various inflammatory proteinases including plasmin, kallikrein, thrombin and urokinase (64). It is approved clinically as mesylate salt in Japan, but not Europe or the USA, for the treatment of chronic pancreatitis and postoperative reflux esophagitis due to its ability to inactivate trypsin and prevent autodigestion (65). Camostat mesylate has demonstrated inhibitory activity against TMPRSS2 and other cell-surface proteases involved in SARS-CoV activation (66). Indeed TMPRSS2 emerged as a promising antiviral drug target after it was identified to have a pivotal role for viral pathogenesis of monobasic H1N1, H3N2 and H7N9 influenza A viruses (67).

Exposure of human bronchial epithelial Calu-3 cells to 10 µM camostat mesylate was reported to cause a 10-fold decrease in SARS-CoV viral entry and a 13-fold decrease in SARS-CoV replication (66). Although from a virology perspective such inhibitory effects are considered mediocre, animal experiments in BALB/c mice at 30 mg/k administered orally twice daily for 9 days starting 10 h before SARS-CoV inoculation increased survival rate to 60 vs. 0% for untreated animals (65). Similarly, Calu-3 cells pre-incubated with camostat mesylate at very high concentrations (100 µM) before infection with SARS-CoV-2 significantly reduced, but failed to abrogate Calu-3 infection with SARS-CoV-2 as measured by SARS-CoV-2-specific RT-PCR (21). Thus, a randomized, placebo-controlled, phase IIa clinical trial (NCT04321096) is evaluating camostat mesylate at 200 mg x 3/day for 5 days as treatment for SARS-CoV-2. However, it is noteworthy that the study design of this trial fails to meet the pre-treatment or, at least, early treatment requirement common to most efficacious antivirals and indeed the in vitro and in vivo performance requirements exhibited previously. Elsewhere, the CLOCC-2020 clinical study (NCT04338906) will evaluate the efficacy and safety of camostat mesylate in combination with the controversial agent hydroxychloroquine in hospitalized patients with moderate COVID-19 infection (56).

Nafamostat, a chemical analog of camostat, has potent inhibitory effects on several types of serine proteases including trypsin, thrombin and plasmin (68) and was identified to effectively reduce the MERS-CoV viral entry in Calu-3 cells at the physiologically relevant concentration of 1 nM (69). Nafamostat at 100 µM demonstrated promising inhibitory effects against SARS-CoV-2 infection of Vero E6 cells (70), but it is anticipated that its very short half-life (71) significantly hinders clinical utility in preventing SARS-CoV-2 infection.

Bromhexine, a widely used mucolytic cough medicine, was identified as a TMPRSS2 inhibitor in a screening on various chemical libraries, including over 1,200 FDA approved drugs. With an IC50 of 0.75 µM, inhibition was reported as selective, with low effects on the related hepsin and matriptase proteases (72). However, preliminary data on influenza-infected Calu-3 cells treated with bromhexine showed no inhibitory effect (73). Despite a lack of in vitro or in vivo data on SARS-CoV-2, it has been proposed as a solution for COVID-19 patients based on its effect on TMPRSS2 and favorable pharmacokinetic and safety profile (74). Several clinical trials are registered to evaluate bromhexine as prophylaxis or therapy in COVID-19 patients using various drug combinations (NCT04355026, NCT04340349, NCT04273763) (56).

Aprotinin is a natural 58 amino acid peptide and a serine protease inhibitor that blocks fibrinolysis and reduces bleeding. It demonstrated significant effects against influenza viruses (75). Preliminary research reports have demonstrated that in Caco2 cells aprotinin is more potent against SARS-CoV-2 (EC50 = 22.9 KIU/ml) than against SARS-CoV (EC50 = 118 KIU/ml) cytopathogenic effects (76) as measured in kallikrein inactivator units (KIU). To this date, no clinical test has been registered in Clinical Trials databases (56).

SARS-CoV nucleocapsid (protein N) binds to cyclophilin A, which subsequently interacts with a member of the immunoglobulin family of receptors, HAb18G/CD147, on the cell membrane leading to viral cell invasion (77), in a mechanism similar with that of HIV-1 virus (78). Based on this model, a humanized anti-CD147 antibody was clinically tested in 17 patients with SARS-CoV-2 (NCT04275245) and published in a preliminary fashion (79). Whilst the results are interesting, interpretation should be approach with caution as the source and characteristics of the antibody, 'meplazumab', are missing, and the number of tested patients is very low.

Clathrin-mediated endocytosis is another mechanism described for SARS-CoV cell invasion and possibly utilized by SARS-CoV-2. Chlorpromazine inhibits the relocation of clathrin and the adaptor protein 2 (AP2) from the cell surface, significantly inhibiting SARS-CoV entry into HepG2 cells at the relatively high concentration of 20 µM (80). Unfortunately, it showed no significant effect on the SARS-CoV-2 cytopathic effects in Vero E6 cells when tested at 100 µM (81), yet a clinical trial is scheduled to test the effect of 25 mg chlorpromazine administrated intravenously every 6 h for 1 week (NCT04354805) (56).

An artificial intelligence method identified members of the numb-associated kinases (NAK) family as potential therapeutic targets against SARS-CoV-2 (82). The AP2-associated protein kinase 1 (AAK1) is an important member of NAK that binds to clathrin and phosphorylates the medium subunit of AP2, playing an important role in regulating clathrin-mediated endocytosis (83,84) and its inhibition was demonstrated to reduce the infectivity of a wide range of viruses (82). The chemically related pyrazole-pyrolopyrimidine derivatives baricitinib and ruxolitinib are clinically approved Janus kinase (JAK) inhibitors with important inhibitory effects on AAK1 (85), likewise predicted to reduce SARS-CoV-2 infection (82). A clinical trial (NCT04348071) is programmed to evaluate ruxolitinib in patients receiving 10 mg twice daily for 14 days and a similar trial (NCT04340232) will test baricitinib administered 2 mg once daily for 14 days (56).

The role of cathepsins in coronavirus entry has been established for SARS-CoV and MERS-CoV. In order to investigate their role in SARS-CoV-2 cell entry a pseudovirus model was tested in ACE2-expressing 293 cells. While cell treatment with the cysteine protease cathepsin B inhibitor CA-074 (30 µM) had no significant effect, cathepsin L inhibitor (SID 26681509, 2 µM) treatment reduced viral entry up to 76%. An inhibitory effect close to 93% was reached after treatment with E64d (30 µM), an inhibitor of calpain and cathepsin B, H and L (86). Cathepsin L is an attractive target for drug development in several diseases, but despite all the efforts, no cathepsin L inhibitor has advanced to clinical trials (87) making future cathepsin L-based SARS-CoV-2 therapies improbable.

Interfering with the endocytic pathway. Most viruses use endocytic entry mechanisms and for the majority of them, a reduction of pH serves as a cell penetration trigger (88). Earlier studies have described that endocytic pH modification suppresses viral replication and may also have a virucidal effect. Such a minimal pH value change, with no negative impact on the patient′s health status, could be achieved by administering a simple small molecule with hydrophobic weak base properties, like ammonium chloride, which would lead to endocellular alkalosis by accumulating in lysosomes following diffusion through plasma and lysosomal membranes. Weak bases and ionophores, like ammonium chloride, chloroquine, or monensin are frequently used in experimental studies of viral cell penetration mechanisms (89). Ammonium chloride treatment strongly inhibited the entry of pseudotypes bearing SARS-2-S in 293T cells lacking TMPRSS2, but was less effi-cient in Caco-2 cells (TMPRSS2+) (21).

Chloroquine, chemically known as 7-chloro-4-((4-(diethy lamino)-1-methyl butyl)amino)quinoline, is a 9-aminoquinoline widely used for the treatment of malaria, amebiasis and several auto-immune diseases (90) recently proposed to be efficient in inhibiting SARS-CoV-2 in infected cells (70,91). Chloroquine has already demonstrated in the past in vitro anti-viral activity against several types of both RNA and DNA viruses, such as rabies virus, poliovirus, several influ-enza virus types, hepatitis A, B and C viruses, Dengue virus, Zika virus, and many others (92), as well as SARS-CoV (93) and MERS-CoV (94). The general anti-viral mechanism of action relates to the ability of chloroquine, as a weak base, to increase the endosomal pH required for viral/host cell fusion, preventing endocytosis, and to interfere with viral particles bound to the cell surface membrane (95). Additionally, in the case of SARS-CoV and SARS-CoV-2, chloroquine is proposed to inhibit the glycosylation of ACE2 receptor chains, thus limiting ligand recognition of these receptors, rendering the viral spike protein unable to mediate cell entry (92).

In light of the new pandemic, several clinical trials have been conducted in different countries in order to test the safety and efficacy of chloroquine phosphate in treating SARS-CoV-2 patients (96), with results confirming a significant improvement when compared to control groups, as in the case of clinical trial ChiCTR2000029609 (97). When confronted with the recent COVID-19 crisis in China, chloroquine has even been included in the national treatment guidelines, with Chinese clinicians recommending 500 mg chloroquine twice daily for 10 days for the treatment of mild, moderate and severe cases of SARS-CoV-2-related pneumonia with no contraindications to the drug (98).

Hydroxychloroquine is a less-toxic derivative of chloroquine also used as an anti-malarial and in the management of auto-immune disease, proposed through in vitro studies to act also on SARS-CoV-2 infected cells (91). In Vero E6 models hydroxychloroquine presented a better antiviral effect with EC50 values of 6.14 µM (after 24 h) and 0.72 µM (after 48 h), compared with chloroquine values of 23.90 µM (24 h) and 5.47 µM (48 h) (91).

Similar to chloroquine in many aspects with the exception of a better pharmacotoxicological profile, hydroxychloroquine is more frequently used instead of chloroquine in COVID-19 clinical trials (99). Several studies confirmed hydroxychloroquine sulfate administration to be significantly associated with a reduction of the viral load in SARS-CoV-2 infected patients, as in the case of the Chinese randomized clinical trial reported by Chen et al (ChiCTR2000029559) (100) and Gautret et al, who also reported after 6 days of treatment apparently significant benefits compared to negative controls when administering daily 600 mg hydroxychloroquine in association with azithromycin, where necessary (101). The drug is currently perceived in certain quarters to be more promising than chloroquine as a COVID-19 treatment due to the reduced probability of causing retinopathy, psychiatric disorders, or severe cardiovascular adverse effects such as arrhythmia (99); however, self-medication using both drugs is unadvisable, as 9-aminoquinolines possess a narrow therapeutic window (102) and are associated with QT prologation. Currently, larger studies with a more flexible design investigate the effect of hydroxychloroquine, with the Solidarity study (EudraCT no. 2020-000982-18) and the Discovery study (NCT04315948) randomizing treatment of SARS-CoV-2-infected patients using different antiviral drugs, including hydroxychloroquine (103). However, preliminary reports are highlighting a 2.61 adjusted hazard ratio of death among COVID-19 patients treated with hydroxychloroquine alone in the absence of azithromycin, and no reduction in the risk of mechanical ventilation (104).

Blocking polyprotein posttranslational processing. Another promising strategy of treatment appears to be interfering with viral replication, especially by acting at key points following translation. After synthesis, the two newly-formed viral polyproteins pp1a and pp1b require for posttranslational processing two important proteinases encoded in these chains of amino acids: papain-like proteinase, PLpro, and chymotrypsin-like proteinase, 3CLpro, often referred to as the main protease or Mpro (3). The activity of these two cysteine proteases is essential for generating the 16 non-structural proteins, critical to the formation of the replicase complex, and it is known that inhibiting the activity of either of these two proteases affects the replication of SARS-CoV-2 (3,105).

Several inhibitors acting on SARS-CoV main protease, which displays 96% similarity to the SARS-CoV-2 Mpro (106), have recently been synthesized and tested both in enzymatic assays and in cell lines, showing promise for developing future drugs. Recently, Zhang et al, after structure-based drug design and optimization of different dipeptide α-ketoamides, derived several potential Mpro inhibitors, of which (S)-N-Benzyl-3-((S)-2-cinnamamido-3-cyclohexylpropanamido)-2-oxo-4-((S)-2-oxopyrrolidin-3-yl) butanamide (referred to as 11r) displayed physiologically rele-vant (nM) antiviral activity against MERS-CoV and SARS-CoV in hepatic (Huh7) but not routine virology (Vero E6) cell lines, as well as good inhibition of the SARS-CoV protease in enzymatic assays (107). Based on previous research, the same study group obtained a pyridone-containing α-ketoamide deriva-tive of 11r, a compound (referred to as 13b) with even lower sub-micromolar concentrations against SARS-CoV-2 Mpro in enzymatic assays, with half-maximal inhibitory concentration (IC50) 0.67±0.18 µM, and low-micromolar EC50 values (4-5 µM) in Calu-3 cells, further obtaining favorable results in mouse studies in terms of pharmacokinetic parameters, reflecting lung tropism after either subcutaneous or topical administration (108).

Drug repurposing appears to be another interesting method of identification of Mpro inhibitors. Most notable drugs showing inhibition of the main protease of SARS-COV-2 were found to be several anti-retroviral agents approved for HIV-1 treatment.

Lopinavir is a selective HIV-1 protease inhibitor orally administered in combination with ritonavir, a CYP3A4 inhibitor used to increase its plasma concentration and clinical efficacy (109). Lopinavir was tested against SARS-CoV and showed a moderate activity in Vero-E6 cells (110). In a preliminary, not yet peer-reviewed, study in Vero E6 cells, lopinavir showed a mediocre EC50 = 5.73 µM against SARS-CoV-2 (111). A recent clinical trial investigating the safety and efficacy of lopinavir (400 mg) and ritonavir (100 mg) effect in 99 patients infected with SARS-CoV-2 has already ended, unfortunately concluding that the administration of these drugs showed no significant benefit comparing to current standard care (112). The ineffectiveness of this combination could be explained by the delayed treatment initiation, the median time from symptoms identification to therapy onset being 13 days (51). Whether the ineffectiveness of the treatment was due to the late therapy start or because of low efficient concentrations at the site of action remains to be explored.

The clinical use of lopinavir/ritonavir is additionally linked to nausea and diarrhea (up to 28%) as well as hepatotoxic effects (2-10%). Despite the limited data to support use in the treatment of COVID-19, there is an important number of clinical studies registered to test the lopinavir (400 mg) and ritonavir (100 mg) coformulation alone or in combination with hydroxychloroquine or interferon (51,56).

Other HIV-1 protease inhibitors, such as amprenavir, tipranavir, saquinavir, ritonavir, nelfinavir, indinavir, darunavir, and atazanavir that have been predicted to inhibit SARS-CoV-2 Mpro (113) were also tested on Vero E6 cells infected to SARS-CoV-2. Among these, nelfinavir was observed to be the most efficient, with a mediocre EC50 of 1.13 µM suppressing viral replication in the post-entry step (111). In a similar study on SARS-CoV, nelfinavir inhibited the viral replication at non-toxic doses with a selectivity index (SI) close to 300, while ritonavir, lopinavir, saquinavir, and indinavir, did not have a significant effect (114). Saquinavir and tipranavir showed mediocre replication inhibition against SARS-CoV-2 in cell lines (EC50 = 8.83 µM, respectively 13.34), although with a lower selectivity index, while amprenavir, darunavir and indinavir had low effects on viral replication with EC50 values over 30 µM (111). Another preprint publication reports the SARS-CoV-2 viral replication inhibition by atazanavir with EC50 values of 2.0±0.12 µM (115).

No clinical study is registered in the Clinical Trials database, nor in the Chinese Clinical Trial Registry to test atazanavir, nelfinavir, tipranavir, or saquinavir as COVID-19 therapies. The clinical trials NCT04252274, NTC04303299 and NCT04366089 will test darunavir in association with other antivirals (56).

Targeting viral RNA-dependent RNA polymerase. The RNA-dependent RNA polymerase (RdRp) is the central subunit of the RNA synthesizing process for all positive-strand RNA viruses and therefore an attractive target for antiviral inhibitors. In SARS-CoV-2 nsp12 functions as RdRp (116) and plays a central role in the viral replication and transcription by catalyzing the synthesis of viral RNA, assisted by nsp7 and nsp8 that serve as co-factors (117). The polymerase of RNA viruses is prone to replication mistakes, lacking the proofreading capacity of its analog from DNA viruses. This high mutation rate (10-3 to 10-5 mutations/nucleotide/round of replication) enables RNA viruses to better adapt to environ-mental changes, but also introduces damaging mutations that corrupt essential functions, a process called lethal mutagenesis (118,119).

In CoVs, nsp14 has both 3′-5′ exoribonuclease (ExoN) and guanine-N7-methyltransferase (N7-MTase) functions. ExoN can hydrolyze RNA acting as a proofreading enzyme that is capable of removing mismatched nucleotides (120). Targeting viral RNA-dependent RNA polymerase has proven a successful strategy in treating various viral infections (121), but is difficult in the case of CoVs because of the ExoN activity (116,119). Importantly, the catalytic site of RdRp shares structural similarities with the hepatitis C virus (HCV) ns5b RdRp (117), introducing the prospect of repurposing ns5b HCV antivirals as COVID-19 therapies. The results of a docking study indicate that tenofovir and sofosbuvir, two approved HCV antivirals, can bind tightly to SARS-CoV-2 RdRp (122). Still, these results should be view with caution considering their effect could be theoretically easily reversed by nsp14 activity. It is thus hypothesized that finding inhibitors of ExoN activity could be a future direction for COVID-19 therapeutics (119).

A number of compounds with proven inhibitory effects on other virus RdRps were tested against SARS-CoV and SARS-CoV-2, triaging some of them to clinical evaluation. Ribavirin has the advantage of being clinically approved, but is associated with important side effects and low efficacy. By contrast, remdesivir, and to a lesser extent, favipiravir and galidesivir, look like the most promising RdRp inhibitors for a future COVID-19 solution.

Remdesivir, formally known as GS-5734, is a 2-ethylbutyl-L-alaninate phosphoramidate prodrug that generates the active compound, GS-441524, a 4-amino-5-cyano-pyrrolotriazine analog of adenosine (123). Remdesivir is metabolized more efficiently than its metabolite GS-441524 into the active nucleoside triphosphate that function as a chain-terminating nucleotide analog blocking RdRp (116). Remdesivir is not approved by the FDA and not by the European Medicines Agency (EMA), but recently received FDA emergency use authorization for the treatment of COVID-19 on the basis of reduced hospitalisation time (124). However, this outcome is not without controversy as the trial primary endpoint was altered days before outcome announcement, raising important concerns with respect to utility under the purported mechanism of action. Given the structural similarity of remdesivir to naturally occurring 2′-O-methyl nucleoside analogues, antagonists of toll like receptor 7, and the initiation of treatment with the pre-symptomatic/early symptomatic optimal treatment window, it is postulated remdesivir may actually affect immunosuppression of cytokine storm syndrome, as opposed to directly acting antiviral effects.

Remdesivir was developed to treat Ebola virus infection, but demonstrated a broad antiviral spectrum against SARS-CoV, MERS-CoV, and various other RNA viruses (116). In Vero E6 cells infected with SARS-CoV-2, remdesivir potently blocked virus infection at high nanomolar concentrations with an EC50 value of 0.77 µM demonstrating a low toxicity as the half-cytotoxic concentration was reported to be above 100 µM (70). A separate study, however, estimated EC50 at 26.90 µM (81). On the other hand, in Caco2 cells remdesivir inhibited SARS-CoV-2 cytopathogenic effects with an EC50 value of 0.23 µM (70). The protective effect was increased 10-fold by the addition of 8 µM of omeprazole. Omeprazole alone has also demonstrated anti-SARS-CoV-2 protective effects, but at physiologically irrelevant concentrations (EC50 = 34 µM), substantially above those used in clinical practice. These results are presented in a yet to be peer-reviewed preprint (76).

Remdesivir was clinically tested in 175 patients in 2018 during the Ebola outbreak in the Democratic Republic of Congo by intravenous administration of 200 mg on day 1 followed by daily maintenance doses of 100 mg from day 2 and continuing for 9 to 13 days. In pediatric patients, the doses were adjusted based on body weight. The study revealed a favorable safety profile with higher mean levels of creatinine and aspartate aminotransferase but failed to achieve its primary endpoint (125).

A case report of the first COVID-19 patient identified in the U.S. presents their treatment with intravenous remdesivir on the seventh day of hospitalization and the improvement of their condition afterward (126). A similar case report described the remdesivir treatment of three hospitalized patients under compassionate use protocol. The patient described as number 6 was the same as the first case report. All three patients tolerated the remdesivir treatment, with transient gastrointestinal symptoms and a serum aminotransferase elevation (127). The administered doses were not mentioned in the article.

A randomized, double-blind, placebo-controlled clinical study (NCT04257656) on confirmed SARS-CoV-2 patients found that remdesivir (n=158, vs. 79 placebo) intravenous administration of a 200 mg loading dose on day 1 followed by 100 mg daily as maintenance doses, up to a 10 days, produced no significant difference in time to clinical improvement. The 28-day mortality was similar between the remdesivir group (14%) compared to placebo (13%). However, remdesivir reduced the time to clinical improvement compared to placebo with a median of 18 vs. 23 days in the placebo group. The study reported no significant impact of remdesivir use on viral load measured on nasopharyngeal and oropharyngeal swabs, implying either no direct acting antiviral effect, or an unexpectedly long SARS-CoV-2 genome half-life (128). This result should be analyzed considering the long average time (10-11 days) from symptom onset to treatment start. We identified a number of other clinical trials that are trying to evaluate the antiviral activity of remdesivir in COVID-19 patients (NCT04252664, NCT04292899, NCT04292730, NCT04302766, NCT04323761, NCT04280705, NCT04321616, NCT04315948, NCT04314817, NCT04349410) using the same doses as NCT04257656 (56).

Favipiravir (6-fluoro-3-hydroxy-2-pyrazinecarboxamide), also known as T-705, was developed as a structural analog of 3-hydroxy-2-pyrazinecarboxamide (T-1105) compound identified in an in vitro anti-influenza virus activity drug screening (129). Favipiravir is a prodrug that is activated by cellular enzyme phosphoribosylation to favipiravir-ribofuranosyl-5′-triphosphate (favipiravir-RTP) (130). It is reported to selectively and potently inhibit the RNA-dependent RNA polymerase of a broad range of RNA viruses: influenza viruses, arenaviruses, bunyaviruses, noroviruses, flaviviruses and filoviruses (131). Favipiravir-RTP functions as a guanosine and adenosine analog, its antiviral activity being significantly inhibited by purine nucleotides and nucleosides, but not by pyrimidine nucleotides in an MDCK cell model. Yet favipiravir and its ribofuranosyl-5′-monophosphate showed no significant inhibitory effect on influenza virus RNA polymerase (100 µM). Favipiravir has a similar structure and also a related antiviral spectrum as ribavirin increasing the lethal mutations in the viral genome; this activity raises concerns about teratogen risk potential (131). The pharmacokinetic profile was characterized in Japanese healthy volunteers to indicate a short half-life of 2 to 5.5 h and urinary excretion in the form of the inactive 5-hydroxy-metabolite (T-705M1) (132). Because of its teratogenicity and embryotoxicity risks, favipiravir was approved in Japan with strict regulations for use only in epidemics (133).

Similar to remdesivir, favipiravir blocked SARS-CoV-2 viral infection in Vero E6 cells, but at almost 80-fold higher concentrations, with a calculated EC50 value of 61.88 µM (70). The results of an open-label comparative controlled study of patients with COVID-19 (ChiCTR2000029600) indicated that patients (n=35) receiving favipiravir (1,600 mg x 2, day 1 and 600 mg x 2, days 2-14) had faster viral clearance and better chest imaging changes than those (n=45) treated for 14 days with lopinavir (400 mg x 2) and ritonavir (100 mg x 2). Both groups also received aerosol inhalation of 5 million U IFN-α twice daily (134). Several clinical trials are registered to test favipiravir in COVID-19 patients (NCT04358549, NCT04346628, NCT04310228, NCT04349241, NCT04336904, NCT04319900, NCT04359615, NCT04333589, NCT04303299, NCT04351295, NCT04356495, NCT04345419) administered orally at a loading dose of 3,200 up to 3,600 mg (1,600-1,800 mg at 12 h) on day-1, followed by 1,200 to 1,800 mg maintenance dose (600-800 mg at 12 h) on days 2-10 (56).

Galidesivir, known also as BCX4430, is an adenosine C-nucleoside analog similar to remdesivir, but has a nitrogen replacing the oxygen in the ribose ring. It is converted in the cell to the corresponding triphosphate nucleotide and after the pyrophosphate′s cleavage to galidesivir monophosphate is incorporated into nascent viral RNA, blocking viral RNA-dependent RNA polymerase chain extension (135,136). It was reported to be active against a wide range of viruses in cell and animal models (137). However, in a HeLa cell model of SARS-CoV infection, galidesivir had an EC50 value of 57.7 µM (135). Considering the high similarity of nsp12 in SARS-CoV-2 and SARS-CoV (12), it was evaluated in Vero E6 cells against SARS-CoV-2, but the inhibition of viral replication was low at 100 µM (81). Nevertheless, a clinical placebo-controlled, randomized study (NCT03891420) will test galidesivir administered intravenously at 12 h intervals for 7 days in COVID-19 patients (56).

A ribonucleoside derivative, β-D-N4-hydroxycytidine (known also as NHC or EIDD-1931), was reported to demonstrate potent inhibitory effects on MERS-CoV, SARS-CoV, and SARS-CoV-2 in Calu-3 and human airway epithelial (HAE) cells. Encouragingly, NHC inhibited SARS-CoV-2 infection in Vero E6 cells with EC50 values of 0.3 µM and a value of 0.08 µM in Calu-3 cells. The isopropyl ester of the prodrug NHC, EIDD-2801, was evaluated in C57BL/6 mice infected with a murine adapted SARS-CoV to reduce significantly the viral titer and associated infection symptoms when administered in doses of 500 mg/kg. The antiviral mechanism of action proposes the inhibition of RdRp, with the effect of NHC being only slightly affected by ExoN proofreading activity (138,139). Despite the potent antiviral profile of EIDD-2801 and its advantage of oral administration development for COVID, use is hindered by the lack of any clinical data.

Ribavirin (1-β-D-ribofuranosyl-1,2,4-triazole-3-carbox amide) is a broad-spectrum antiviral agent clinically used primarily for treating hepatitis C. The antiviral mechanism is complex, the most important effects being the inhibition of human cells inosine monophosphate dehydrogenase (IMPDH) by the monophosphate derivative of the drug, and the incorporation of ribavirin 5′-triphosphate in the nascent viral genome by RdRp (25). Both ribavirin and favipiravir act as guanine analogs due to their carboxamide group that attaches to cytosine by hydrogen bonds (137).

In cell models of SARS-CoV infection ribavirin had a limited effect on viral replication (110). Similarly high concentrations are needed to block SARS-CoV-2 viral infection in Vero E6 cells (EC50 = 109.5 µM) (70) limiting clinical potential against COVID-19. The resistance of SARS-CoV and SARS-CoV-2 to ribavirin is produced by ExoN′s proofreading activity during virus replication (119).

A systematic review of the therapies tested in the SARS-CoV outbreak of 2002-2003 found that among the 20 studies on ribavirin, results were inconclusive, with no discernible clinical differences to other treatments. The review highlights various toxic effects presented by several studies, the most frequent being hemolytic anemia and liver dysfunction (140). The high doses needed to reduce the viral replication highlight important toxic effects limiting the therapeutic potential of ribavirin treatments in COVID-19 cases. Despite these reservations, an open-label, non-randomized, clinical trial (NCT04356677) is programmed to test aerosolised administration of ribavirin twice daily for up to 6 days at 50 mg/ml or 100 mg/ml concentrations (56). A combination of lopinavir (400 mg), ritonavir (100 mg), ribavirin (400 mg), and IFN-β 1b (0.25 mg) is additionally under evaluation (NCT04276688) (56).

Targeting cellular signaling pathways. Viruses highjack host cell-signaling pathways, redirecting cellular processes in favor of their survival and replication, interfering with normal cell metabolism, survival, by interrupting transcription and replication (141). There are complex and not completely understood mechanisms of viral interference with cell signaling pathways. In the case of SARS-CoV-2, precise information is scarce and amplified by the large number of proteins of unknown function encoded in the virus genome, but research on new potential therapies can successfully use knowledge gained on the related SARS-CoV and MERS-CoV outbreak pathogens.

In cells infected with MERS-CoV perturbation of several regulatory kinases was detected, such as the increased phosphorylation of Akt1 and mTOR, modifications that have been linked to a decrease in autophagy (142). Thus, the virus is believed to block autophagy through a complex mechanism dependent on viral nsp6 that involves phosphorylation of S-phase kinase-associated protein 2 (SPK2) by a complex involving FK506-binding protein 51 (FKBP51), PH domain leucine-rich repeat-containing protein phosphatases (PHLPP), Akt, and Beclin1 (BECN1). The activated SPK2 promotes the ubiquitination of BECN1 leading to its proteasomal degradation and inhibition of autophagy (103). A yet to be peer-reviewed report has proposed that SARS-CoV-2 infection may strongly reduce autophagic flux in experimental models of human bronchial epithelial cells NCI-H1299 and VeroFM cells (143). The analysis of Vero E6 cells infected with SARS-CoV revealed higher levels of Akt phosphorylated at serine 473 (S473) residue, but not at threonine 308 (T308) (144). The anti-apoptotic effect of Akt depends on both S473 and T308 phosphorylation (145) explaining low anti-apoptotic response to SARS-CoV infection (144). These observations highlight the potential of targeting SKP2 or the PI3K/AKT/mTOR pathway.

MK-2206 is a selective and highly potent inhibitor of all three Akt isoforms, currently under clinical evaluation against various oncologic diseases (145). It reduced SARS-CoV-2 proliferation in VeroFM cells with a noteworthy EC50 value of 0.09 µM measured after 24 h in plaque-forming units (143). This antiviral potential of MK-2206 expands upon the previously reported activity on influenza pH1N1 at EC50 values in the micromolar range (146).

Several protein kinase inhibitors targeting the ERK/MAPK and PI3K/AKT/mTOR signaling pathways were tested in Huh7 cells infected with MERS-CoV. Pretreatment with 10 µM sirolimus (also known as rapamycin), an inhibitor of mTOR, reduced viral infection by a mediocre 61%, while postinfection treatment effected a comparable 57% reduction. Everolimus, a 2-hydroxyethyl derivative of sirolimus, had similar inhibitory effects at 10 µM (56% reduction in pre-treated cells and 59% in postinfection treatment) (147). Surprisingly, the treatment of VeroFM cells with 0.3 µM sirolimus increased the SARS-CoV-2 infection (143). Presently, a clinical trial (NCT04341675) is scheduled to assess sirolimus administered as 6 mg on day 1, followed by 2 mg daily for the next 13 days (56). Metformin could be another repurposed drug for COVID-19 based on its autophagy induction by activation of AMP-activated protein kinase (AMPK) and inhibition of mTOR (148,149).

Niclosamide is an oral antihelminthic drug used to treat a large array of parasitic infections being included on the WHO list of essential medicines (150). In a screening of marketed drugs it was identified to protect Vero E6 cells from the cytopathic effects of SARS-CoV (151). Niclosamide inhibited SARS-CoV replication in Vero E6 cells with a corresponding EC50 value under 0.1 µM, as measured by spike protein quantification (152). A yet not peer-reviewed preprint presents the SARS-CoV-2 growth inhibition of niclosamide with an EC50 value of 0.17 µM. The authors proposed a mechanism of action that implicates the inhibition of SPK2 (143). SPK2 inhibitors reverse the reduction of BECN1 levels produced by SARS-COV-2 in host cells and enhance autophagy, inhibiting the viral replication (142,143). Another possible mechanism could be niclosamide′s protonophore effect resulting in endosomal pH neutralization preventing acid-dependent virus replication (153). The maximum plasma concentration after 500 mg x 3/day oral administration of niclosamide ranged from 35.7 to 182 ng/ml, equivalent to 0.1-0.55 µM (154). The results showed poor oral bioavailability that could hinder immediate clinical utility against COVID-19. The clinical trial NCT04372082 will evaluate niclosamide 500 mg x 4/day (day 1) followed by 500 mg x 2/day (days 2-10) in combination with diltiazem 60 mg x 3/day (days 1-10) (56). The use of diltiazem is supported by host-targeted antiviral effects demonstrated in influenza mouse models (155).

Nitazoxanide, known as 2-(acetyloxy)-N-(5-nitro-2-thiazolyl)benzamide, is a structural analog of niclosamide. Nitazoxanide is an antiprotozoal agent with proven broad-spectrum antiviral properties. It is a prodrug activated to its desacetyl derivative, tizoxanide, by hydrolysis. Both nitazoxanide and tizoxanide inhibited MERS-CoV replication in LLC-MK2 cells with mediocre EC50 values of 2.99 µM (0.92 µg/ml) and 3.13 µM (0.83 µg/ml), respectively (156). Nitazoxanide displayed similar effects on SARS-CoV-2 cultured in Vero E6 cells with an EC50 = 2.12 µM (70). The antiviral mechanism is possibly the same as niclosamide, as observed in RAW264.7 cells treated with tizoxanide. Tizoxanide increased BECN1 expression, inhibited Akt and mTOR, and promoted the formation of autophagy vacuoles (157). A placebo-controlled study (NCT04343248) is scheduled to evaluate nitazoxanide (300 mg x 2/day) as post-exposure prophylaxis for COVID-19 elderly patients, and a related study (NCT04359680) is focused on healthcare workers. Other clinical studies will test nitazoxanide in combination with hydroxychloroquine or with ivermectin (56).

Valinomycin is a toxic natural dodecadepsipeptide that also inhibits SPK2 and blocked SARS-CoV replication in Vero E6 cells (EC50 = 1.63 µM) (152).

Antiviral mechanisms. Umifenovir (also known as arbidol) is a broad-spectrum antiviral agent targeting both DNA and RNA, and both enveloped and non-enveloped viruses, currently used clinically for the prophylaxis and treatment of influenza in Russia and China. The antiviral mechanism is not known and is hypothesized to be directly virucidal coupled with host-targeting effects (158,159), i.e., potentially polypharmacological in nature. In a retrospective study on COVID-19 patients, 16 people received umifenovir 200 mg x 3/day, and 34 patients were treated with the lopinavir (400 mg)/ritonavir (100 mg) combination. The umifenovir group had a shorter duration of positive SARS-CoV-2 RT-PCR tests, suggesting that umifenovir monotherapy was more effective than lopinavir/ritonavir in reducing viral load in COVID-19 patients (160). Separately, a retrospective cohort study analyzed 16 patients who received umifenovir and lopinavir/ritonavir versus 17 patients that received lopinavir/ritonavir and found an apparent favorable clinical response in the former group (161). In a retrospective study on 45 patients treated with 200 mg umifenovir three times a day for 5 days in 8 patients and 7 up to 10 mg in the other 37 patients, no severe side effects were observed. The median time from admission to the first negative test and hospitalization time was longer compared to the control group, indicating that umifenovir alone may not accelerate SARS-CoV-2 clearance (162).

The antiviral effect of umifenovir was only recently investigated on Vero E6 infected with SARS-CoV-2. Umifenovir treatment reduced the viral cytopathic effects with an EC50 value of 4.11 µM, but with a relatively low selectivity (SI=7.73). After a single oral dose of 800 mg, the maximal plasma concentration in man was ascertained at ~4.1 µM. These data suggest that the doses of 200 mg three times a day are too low for a physiological relevant antiviral effect (163).

Ivermectin represents a mixture of two semisynthetic avermectins and belongs to the chemical family of 16-membered macrocyclic lactones. It is used for over three decades to treat various parasitic infections being included on the WHO list of essential medicines (164). The antiviral effects of ivermectin on various RNA viruses like influenza, Dengue virus, or West Nile Virus prompted its evaluation against SARS-CoV-2. Vero/hSLAM cells were infected with SARS-CoV-2 and treated with 5 µM ivermectin. After 24 h the viral RNA was reduced by 93% in the supernatant and by 99.8% in the cells. After 48 h of treatment, the viral RNA decrease was close to 5,000x (165). The EC50 value was determined to be ~2 µM and the hypothesized mechanism of action implicated blockade of viral protein transport in the nucleus by dissociation of the host importin α/β1 heterodimer (165,166) - mechanism not in line with the exclusively cytosolic life cycle of SARS-CoV-2. Ivermectin is most frequently used for onchocerciasis, strongyloidiasis, and enterobiasis in doses of 150 to 200 µg/kg, and up to 400 µg/kg in patients with lymphatic filariasis (167). A clinical study (NCT04343092) is programmed to test iver-mectin in COVID-19 patients as a single dose of 200 µg/kg in combination with daily doses of hydroxychloroquine (400 mg) and azithromycin (500 mg). Two other clinical trials are registered to test ivermectin, one in combination with chloroquine (NCT04351347), and another (NCT04360356) in association with nitazoxanide (56).

Emetine is a natural tetrahydroisoquinoline alkaloid from ipecac species with potent inhibitory effects on the replication of a broad range of DNA and RNA viruses. Emetine displayed potent anti-MERS-CoV activity in Vero E6 cells, with an EC50 = 0.34 µM (after 72 h) and SI=9.06 (168). The EC50 value against SARS-CoV-2 was evaluated as 0.5 µM after 48 h, a concentration almost 3-fold higher than emetine′s therapeutic plasma concentration (81), hindering its clinical use in COVID-19 patients. Lycorine is a structurally related alkaloid found in Amaryllidaceae species, with potent anti-MERS-CoV effects (EC50 = 1.63 µM), but with therapeutic doses that exceed the toxic ones (168). Homoharringtonine is an alkaloid approved as a prodrug derivative, omacetaxine mepesuccinate, for chronic myeloid leukemia treatment. It yields potent and broad anti-RNA virus effects by reducing the phosphorylation level of the eukaryotic initiation factor 4E (eIF4E) (169). Homoharringtonine reduced SARS-CoV-2 viral load in Vero E6 cells with an EC50 value of 2.10 µM (81). Zotatifin (eFT226) is an inhibitor of eukaryotic initiation factor 4A (eIF4A) under evaluation for advanced solid tumor malignancies and produced strong antiviral effects in Vero E6 cell models of SARS-CoV-2 viral infection (170).

A number of antiviral compounds were evaluated against SARS-CoV-2 with disappointing results. Oseltamivir, a neuraminidase inhibitor frequently used for influenza patients showed no significant antiviral effects at concentrations under 100 µM in Vero E6 cell models. The same result was obtained for baloxavir acid, the active form of the baloxavir marboxil prodrug. In influenza viruses it has been reported to block viral RNA synthesis by inhibiting endonuclease activity (81). Other influenza neuraminidase inhibitors such as laninamivir, peramivir, and zanamivir had no result on the cytopathic effects of SARS-CoV-2 activity even at high concentrations (163).

Modulation of the immune defense. The response induced by viruses in the human host is a combination of innate and acquired immunity that unfolds in a sequence, well known in many aspects, but considerably nuanced between distinct insults. Thus, foreign matter recognition initiates lympocyte recruitment, to progresses into a resolution phase that normally seeks to return to homeostasis (171). The inflammatory response to SARS-CoV-2 generally begins when pathogen-associated molecular patterns (PAMP), such as viral RNA, and damage-associated molecular patterns (DAMPs), including ATP, DNA, and ASC oligomers, are recognized by cell surface and cytosolic PAMP recognition receptors (PRRs). The ensuing secretion of pro-inflammatory cytokines and chemokines, such as IL-6, IFN-γ, monocyte chemoattractant protein 1 (MCP1), and CXCL10, attracts monocytes and T lymphocytes, but, unusually, not neutrophils, to the infected site (172). The impact of cytokines is generally increased in obesity, which is associated with higher baseline inflammatory status, explaining the higher risk of complications for obese patients infected with SARS-CoV-2 (173).

The cytokine IL-6 is one of the most important acute inflammatory mediators secreted early during an infection, along with IL-1 and TNF-α (174). Immunosuppressants targeting these molecules are needed to reverse the rampant immune activation observed in late stage, severe forms of COVID-19 (175). A comprehensive list of immunosuppressive therapies aimed at limiting immune-mediated damage produced by SARS-CoV-2 infection are presented in Table I.

Table I

Immunosuppressive therapies in COVID-19.

Table I

Immunosuppressive therapies in COVID-19.

ClassDrugMechanisms of actionDosesClinical studies
IL-6TocilizumabHumanized mAb that binds selectively and competitively to soluble and membrane-expressed IL-6 receptors, blocking IL-6 signal transduction (176)Several posologies, e.g., in dose of 8 mg/kg (up to a maximum of 800 mg per dose) within no less than 60 min, with an interval of 12 h (56)NCT04317092, NCT04345445, NCT04331795,
NCT04332094, NCT04346355, NCT04359667,
NCT04372186, NCT04320615, NCT04332913,
NCT04335071, NCT04356937, NCT04363853,
NCT04363736, NCT04361032, NCT04310228,
NCT04306705, NCT04335305, NCT04315480,
NCT04370834, NCT04339712, NCT04333914,
NCT04361552, NCT04330638, NCT04331808,
NCT04322773, NCT04347031, NCT02735707 (56)
SarilumabHuman mAb, IgG1, directed against IL-6R (177)Doses of 400 mg, in 2 subcutaneous injections or by intravenous route (56)NCT04357808, NCT04315298, NCT04341870,
NCT04357860, NCT04327388, NCT04359901,
NCT04324073, NCT04322773, NCT04345289 (56)
SiltuximabChimeric anti-IL-6 mAb.11 mg/kg administered by intravenous infusionNCT04329650, NCT04322188, NCT04330638 (56)
ClazakizumabHumanized rabbit mAb, anti-IL-625 mg intravenous single dose, possibly repeatedNCT04351724, NCT04363502, NCT04343989,
NCT04348500 (56)
IL-1,AnakinraIL-1R natural antagonist, reproduced industriallyAdministered 400 mg from day 1 to day 3 (two injections of 100 mg each 12 h) and 200 mg the remaining 7 daysNCT04366232, NCT04364009, NCT04357366,
IL-1βNCT04324021, NCT04339712, NCT04362111,
NCT04341584, NCT04330638, NCT02735707 (56)
CanakinumabmAb, IL-1β antagonist300 or 600 mg (4 or 8 mg/kg)NCT04365153, NCT04348448, NCT04362813) (56)
TNF-αXPro1595A protein biologic that targets soluble TNF (sTNF)1 mg/kg for 2 weeksNCT 04370236 (56)
AdalimumabHuman mAb against TNF-α.Not availableChiCTR2000030089 (178)
IFN-αIFN-α 2a, IFN-α 2b nasal, aerosolsType I IFNRecombinant human IFN-α 1b nasal drops, 2-3 drops for each nostril per time, 4 times/day IFN-α 1b in aerosols 10 million units twice dailyNCT04320238, NCT04275388, NCT04293887,
NCT04251871, NCT04344600, NCT04349410,
NCT04295551 (56)
IFN-βIFN-βType I IFN, which has the same receptors as INFαIFN-β 1b 8 million units per day, day 1-3NCT04350671, NCT04343768, NCT04350684,
NCT04350281, NCT04366245, NCT04324463,
NCT02735707, NCT04276688, NCT04315948 (56)
IFN-λPegylated IFN-λType III IFN180 µg subcutaneous injection of pegylated IFN-λNCT04343976, NCT04354259, NCT04344600 (56)

IL-6 is produced in response to acute inflammation, primarily in response to stimulation by TNF-α, lipopolysaccharides, and IL-1 (179). The cellular sensor for IL-5 is the surface-expressed IL-6 receptor (IL-6R; classical signaling pathway) or through soluble IL-6R (trans-signaling pathway) (180). The first pathway could be anti-inflammatory as IL-6 plays a pivotal role in the polarization of immune responses toward Th1, inhibiting the production of IFN-γ by CD4 T cells, and by consequence CD8 T cell activation (174). The signaling through soluble IL-6R has different consequences. The complex of IL-6 and soluble IL-6R can bind to a membrane structure named gp130 on cells that do not express IL-6R, initiating what appear to be pro-infammatory cascades in cells otherwise non-responsive to IL-6 (181).

Several studies report elevations in IL-6 levels in patients with COVID-19 (45,182,183). A retrospective study on 191 hospitalized COVID-19 patients from the Wuhan region found higher IL-6 levels in the non-survivor group, compared to survivors (184). A meta-analysis study reported a 2.9-fold higher level of IL-6 in difficult COVID-19 cases in contrast to non-complicated ones (185). IL-6 has also an essential role in the pathophysiology of rheumatoid arthritis being a validated target for rheumatoid arthritis therapies (186), driving drug repurposing studies for the IL-6 mediated-management of COVID-19.

Tocilizumab is a humanized monoclonal antibody (mAb) directed against the IL-6 receptor used as an effective therapeutic agent for rheumatoid arthritis patients who do not respond to methotrexate (176). A retrospective analysis of published studies involving the use of tocilizumab in patients with COVID-19 highlighted the importance of close patient monitoring for neutropenia, thrombocytopenia, and elevated liver enzymes (187). A pilot prospective open, single-arm study evaluated tocilizumab in 63 hospitalized patients with severe COVID-19 to report improved respiratory and laboratory parameters (188). Sarilumab is a fully humanised monoclonal antibody that specifically binds to both soluble and membrane-bound IL-6 receptors (189). Siltuximab and clazakizumab are antibodies targeting IL-6 that are under clinical evaluation for severe lung disease associated with SARS-CoV-2 infection (190).

IL-1 receptor signaling is implicated early in infection, preceeding IL-6 expression. However, it is also responsible for acute tissue inflammatory damage. In mice, the cytokine storm is associated with elevated levels of IL-1 (174), and a potentiation of TNF-α (191). Using anakinra, the synthetic form of natural IL-1 receptor antagonist, it has been shown in mice that IL-1 signalling blockade could be a potential treatment of influenza infections, arresting airway neutrophilia early in the infection cycle, but also during the peak of viral replication (192).

TNF-α is a key component of the cytokine response and is implicated in COVID-19 severity, as it is found at elevated levels among severe cases (45). There is considerable clinical experience globally with several antibodies targeting TNF-α in clinic against severe cases of autoimmune inflammatory disease, such as rheumatoid arthritis, Crohn's disease, ankylosing spondylitis, or psoriasis (193). The idea of repurposing anti-TNF-α immunotherapies for the management of COVID-19 is supported by preclinical studies on influenza mouse models (193). Adalimumab, a fully humanised monoclonal antibody, is under evaluation in COVID-19 patients (185).

Activation of the nicotinic receptor α7 on immune cells also reduces the levels of IL-6 and TNF-α (171). Based on this effect, it has been hypothesized that nicotine, a cholinergic agonist, could have protective effects in COVID-19 patients (194). However, it is unlikely that nicotine can be used clinically due to its addictive effects and lack of specificity (171). Rather, a review based on the available literature on the impact of smoking on COVID-19 identified a number of studies highlighting a history of smoking as a prognostic factor for severe outcomes, while a meta-analysis study found no significant correlation between smoking and the severity of COVID-19 disease (195).

The interferon family, whose expression is induced directly and indirectly following viral PAMP recognition, is critical in directing innate and adaptive immunity direction. Thus, the interferon cascade induces multiple host antiviral factors or immunomodulators. Activation of either of the two members of the IFN-α receptor (IFNAR) family initiates cytosolic signal-ling cascades culminating in the transcriptional activation of numerous IFN-stimulated genes (ISGs). The protein products of these transcripts exhibit antiviral principally through inhibition of viral replication. Furthermore, type I IFNs enhance natural killer cell activity and antiviral T cell responses, which are central to antiviral defence (196).

A comprehensive evaluation of the therapies tested in the SARS-CoV outbreak found two studies reporting IFN-α therapies in combination with steroids and/or ribavirin, without a significant difference in the clinical outcome when compared to other therapies used (140). A preprint report suggests a higher susceptibility of SARS-CoV-2 to type I IFN treatment compared to SARS-CoV (197). These results were reaffirmed on Vero cells treated with IFN-α or IFN-β, returning EC50 values for SARS-CoV-2 at 1.35 IU/ml for IFN-α, and 0.76 IU/ml for IFN-β. In contrast, SARS-CoV EC50 values were reported to range between 95 to 105 IU/ml depending on the viral strains used (198).

Several immunosuppressants are also being examined as potential solutions for severe COVID-19, with the highest interest being in drugs such as methotrexate, JAK inhibitors (ruxolitinib, baricitinib, tofacitinib, imatinib), colchicine, thalidomide, and lenalidomide. Methotrexate-loaded nanoparticles administered intravenously at 20 mg, once per week (total of 4 doses), is under evaluation in one trial (NCT04352465) (56). Imatinib, an Abl kinase inhibitor and to a lesser extent, a JAK/STAT inhibitor, is used as an experimental drug in elderly COVID-19 patients in out-of-hospital settings at doses of 400 mg/day, 7 days (NCT04346147, NCT04357613, NCT04356495) (56). Colchicine presents long-established anti-inflammatory properties and neutrophil inhibitory effects and is currently under evaluation in COVID-19 patients (NCT04322682, NCT04322565, NCT04328480, NCT04326790, NCT04350320) (184,199). Thalidomide plus low doses of glucocorticoids, umifenovir, and IFN-α aerosols have been used in NCT04273581 and NCT04273529. Lenalidomide, a structural derivative of thalidomide, is currently under evaluation as 4 mg/day on days 1, 3 and 5, in less severe cases of COVID-19 associated with low-molecular weight heparin (NCT04361643) (56). Eculizumab is a recombinant humanized monoclonal antibody that targets complement component 5 and is under clinical study in 900-1200 mg doses administered intravenously (NCT04355494) (56).

Dietary supplements. Ascorbic acid or vitamin C is an established antioxidant and reactive oxygen species scavenger widely considered to alleviate or prevent infections (200). Vitamin C was proposed as a supportive treatment for COVID-19 and several clinical trials are registered to assess its effects. The clinical study NCT04323514 uses intravenous administration of 10 g of vitamin C, while study NCT04342728 uses 8 g of ascorbic acid divided into 2-3 doses/day alone or combined with 50 mg of zinc gluconate, and the NCT04344184 study uses 100 mg/kg vitamin C intravenously administered every 8 h for up to 72 h (56). An article details a Chinese expert report on clinical improvement of 50 moderate to severe COVID-19 patients treated intravenously with 10-20 g/day (201). Vitamin D influences the immune response by modulating several immune pathways and its deficiency was correlated with increased risks of respiratory infections (202). The clinical study NCT04334005 will test administration of a single dose of 25,000 IU of vitamin D as supplement in addition to standard therapies, while in NCT04334005 vitamin D will be given orally as 50,000 IU once weekly for 2 weeks in combination with 81 mg of acetylsalycilic acid (56). Zinc has anti-inflammatory effects moderating T cell functions that could limit excess cytokine production in COVID-19 patients (203). Selenium supplementation was shown to increase immunity and could be used in SARS-CoV-2 infections (204). The clinical study NCT04323228 is scheduled to test an oral supplement enriched in eicosapentaenoic acid, gamma-linolenic acid containing 18 µg selenium and 5.7 mg zinc (56).

Oligonucleotide and gene therapy-based approaches. With the precise mechanism of SARS-CoV-2 migration from respiratory epithelia onto distal ACE2-expressing organs remaining unclear, direct intervention at the RNA genome level of SARS-CoV-2 is also attracting research attention. However, efforts in this space, compared to the advanced nature of vaccine and small molecule intereventions, can only be characterized as speculative and preliminary.

The most clinically advanced drug classes in this space are short interfering RNA (siRNA) and ribonuclease H (RNaseH)-active oligonucleotide antisense therapeutics, modalities that have enjoyed serial regulatory approval successes and become commercially viable since 2016. Thus, first pass metabolism affords adequate passive liver uptake after systemic administration to tackle hereditary hepatic diseases [e.g., mipomersen (205)]. Similarly, intrathecal administration of antisense has proven an effective intervention against spinal muscular atrophy [nusinersen (206)] and ushered true n-of-1 medicine [milasen (207)]. Yet all clinical candidates evaluated between 2000-2011 for lung diseases of inflammatory or viral nature achieved ambiguous and inadequate outcomes, despite the apparent facility of topical dosing to the airways (208). This has been largely attributed to misconceptions around systemic bioavailability and topical cytosolic delivery potential, as rodent studies of oligonucleotide bioavailability following respiratory dosing (32) reflect allometrically scaled human pharmacokinetics even onto demonstrating effective hepatic and kidney targeting (32,209). Does this preclude topical intervention to prevent ACE2 receptor docking of SARS-CoV-2? Unfortunately, even the single clinical stage antisense candidate AZD1419 targeting the cell surface TLR9 to improve time-to-loss of eosinophilic, moderate-to-severe asthma control, also reportedly failed to meet primary endpoints in the phase 2a INCONTRO trial (NCT02898662) (56). Although clarity over respiratory TLR9 coverage by the adopted dosing regime remains undetermined, direct comparisons are ill-advised, thus focusing future intervention efforts in four areas.

At first instance, aptamer-mediated inhibition of ACE2 binding and TMPRSS2 activity, either solely or as a combination therapy, presents a rational means of intervention to prevent viral adhesion and cellular entry, similar to that proposed by small molecule inhibitors. Although cost of goods, chemistry, manufacturing and control requirements are significantly higher for this chemotherapeutic class vs small molecule drugs, rapid hit generation by modern aptamer development methods (210,211) and established orthogonal aptamer optimization strategies can deliver clinical candidates compatible with scalable manufacturing pertinent to pandemic outbreaks, in timelines comparable or better than antibody biotherapeutics. Thus, in the event of complete failure across the vast number of repurposed medication trials described in this review, a second wave of aptamer-based treatments could be ready for subsequent clinical testing. Significantly, systemic access achieved through the lung (32) may afford distal tissue protection from SARS-CoV-2 infection.

The following approaches would involve the generation of antisense, siRNA chemo- and biotherapeutics (DNA Directed RNA interference mediators in the form of short hairpin RNA (shRNA) precursors), or CRISPR-CAS13 systems (212) that would seek to directly cleave the RNA genome of SARS-CoV-2. Cytosolic delivery challenges notwithstanding, the paucity of reports indicating multi-log suppression of viral replication by these chemotherapeutic classes irrespective of target RNA virus, and the diverse evidence of rapid viral evolutionary escape, combination therapy is likely to be necessary (213) to afford either protection, or treatment against SARS-CoV-2 by any such agents. In this respect, RNA-cleaving CRISPR-CAS13 systems suffer from macromolecular ribonucloprotein complex requirements that compound drug delivery challenges vs the relatively smaller molecular weight of oligonucleotides, that rely on host proteins to exert their mechanism of action.

Poignantly, the only modality proven to achieve cytosolic delivery in the lung are adeno-associated virus 6 biotherapeutics (214,215) for the minigene treatment of cystic fibrosis (216). Although this drug class has yet to be attempted against viral respiratory diseases, the safety of AAV-mediated triple anti-viral shRNA expression has been demonstrated in man even onto phase IIb against HCV (NCT01899092). Consequently, a brief anti-SARS-CoV-2 shRNA discovery and optimization campaign coupled to promoter optimization experiments (217) in physiologically relevant organoid models could yield a high confidence-in-safety and confidence-in-rationale candidate drug with the potential to suppress viral escape (218) if adequately tuned to express shRNAs in vivo without interrupting microRNA homeostasis. Significantly, the approach benefits from a ′fire and forget′, single, inhaled administration that would mediate transgene expression within 3 days of dosing and for up to 6 months (217), or potentially longer. It is, therefore, proposed that such an intervention may compensate for broad-spectrum, short-term protection from SARS-CoV-2 infection in high risk populations in the event of failure to deliver protective vaccines, or vaccination ineligibility due underlying immunosuppression.

5. Discussion

Assembling this review was an exciting and laborious daunting task, considering the astonishing volume of research published and the urgency of finding effective, yet safe, therapeutical solutions for COVID-19. The high pressure on the research community leads both to very good studies and publications, but also hasty and poorly designed studies, biased conclusions, or unproven hypotheses, all mixed together. The research directions were heavily influenced by the evolution of the COVID-19 epidemic. At the early stages of the outbreak in China, patients received oseltamivir based on the erroneous diagnosis of influenza. Even if neuraminidase, the target of oseltamivir, was invalidated for COVID-19 treatments, several ongoing clinical trials still include oseltamivir as a comparison group (51).

Repurposing was also a rapid response solution based on the experience with SARS-CoV, MERS-CoV, or with other viruses. Many of the repurposed drugs undergoing clinical trials were not tested in cell models against SARS-CoV-2, raising questions about their real efficacy. Even so, the cell models can be misleading because most compounds have not been tested on human cells and because only EC50 values are reported without clear information on the dose-response curve. Several conditions such as different multiplicities of infection or time of exposure can dramatically influence the EC50 values. There are several other concerns that are worth mentioning: the potential of a drug to reach the target tissue and how it would perform under complex, disease-altered conditions (Fig. 4).

Future research should focus on how the virus evades the immune response and try to better understand its interaction with the T and B cell responses, both in the humans and experimentally infected animals. The second goal should be to reveal and assess details of viral replication strategies and pathways, determining the relationship between sites of viral RNA replication and virus assembly, as well as the extent to which virus-host interactions are SARS-CoV-2 specific and organ-specific, using genomics and proteomics, as well as new reagents. A third future goal should be to translate new information about the structure and function of SARS-CoV-2 proteins into specific anti-virus therapies, particularly with respect to the SARS-CoV-2 proteins of unknown function. The next goal will be the understanding of viral pathogenesis, to design and develop effective live or attenuated safe vaccines. It is anticipated that, like other RNA viruses, subgenomic SARS-CoV-2 replicon systems adapted to lung, kidney, and even neuronal cell types will catalyse the understanding of SARS-CoV-2 biology.


No funding was received.

Availability of data and materials

Data sharing is not applicable to this article, as no datasets were generated or analyzed during the current study.

Authors′ contributions

Conception: GMN, AT. Acquisition of data, design and writing: GM, HP, SAM, DP, GN, GNDI, DAS, TKN, ND, AT. All authors have read and approved the final manuscript.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

SAM is the CSO and Founder of PulmoBioMed Ltd., a Northumbria University spin out company but had no personal interest in product promotion, or any influence in terms of the content of this article. DAS is the Editor-in-Chief for the journal, but had no personal involvement in the reviewing process, or any influence in terms of adjudicating on the final decision, for this article. The other authors declare that they have no competing interests.



adaptor protein 2


AMP-activated protein kinase


Ang1-8 receptor 1


angiotensin-converting enzyme 2


AP2-associated protein kinase 1




coronavirus disease 2019


European Medicines Agency




half-maximal effective concentration


half-maximal inhibitory concentration






Janus kinases


Middle East respiratory syndrome virus


monoclonal antibody


monocyte chemoattractant protein 1


non-structural proteins


numb-associated kinases


open reading frames


receptor binding domain


recombinant human ACE2


RNA-dependent RNA polymerase


single nucleotide polymorphisms


S-phase kinase-associated protein 2


Toll-like receptor


tumour necrosis factor alpha


type II transmembrane protease serine 2


US Food and Drug Administration


Not applicable.



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Nitulescu GM, Paunescu H, Moschos SA, Petrakis D, Nitulescu G, Ion GN, Spandidos DA, Nikolouzakis TK, Drakoulis N, Tsatsakis A, Tsatsakis A, et al: Comprehensive analysis of drugs to treat SARS‑CoV‑2 infection: Mechanistic insights into current COVID‑19 therapies (Review). Int J Mol Med 46: 467-488, 2020
Nitulescu, G.M., Paunescu, H., Moschos, S.A., Petrakis, D., Nitulescu, G., Ion, G.N. ... Tsatsakis, A. (2020). Comprehensive analysis of drugs to treat SARS‑CoV‑2 infection: Mechanistic insights into current COVID‑19 therapies (Review). International Journal of Molecular Medicine, 46, 467-488.
Nitulescu, G. M., Paunescu, H., Moschos, S. A., Petrakis, D., Nitulescu, G., Ion, G. N., Spandidos, D. A., Nikolouzakis, T. K., Drakoulis, N., Tsatsakis, A."Comprehensive analysis of drugs to treat SARS‑CoV‑2 infection: Mechanistic insights into current COVID‑19 therapies (Review)". International Journal of Molecular Medicine 46.2 (2020): 467-488.
Nitulescu, G. M., Paunescu, H., Moschos, S. A., Petrakis, D., Nitulescu, G., Ion, G. N., Spandidos, D. A., Nikolouzakis, T. K., Drakoulis, N., Tsatsakis, A."Comprehensive analysis of drugs to treat SARS‑CoV‑2 infection: Mechanistic insights into current COVID‑19 therapies (Review)". International Journal of Molecular Medicine 46, no. 2 (2020): 467-488.