Open Access

Potential immunomodulatory effects of vitamin D in the prevention of severe coronavirus disease 2019: An ally for Latin America (Review)

  • Authors:
    • Francisco Javier Turrubiates‑Hernández
    • Gabriela Athziri Sánchez‑Zuno
    • Guillermo González‑Estevez
    • Jorge Hernández‑Bello
    • Gabriela Macedo‑Ojeda
    • José Francisco Muñoz‑Valle
  • View Affiliations

  • Published online on: February 1, 2021     https://doi.org/10.3892/ijmm.2021.4865
  • Article Number: 32
  • Copyright: © Turrubiates‑Hernández et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Currently, the world is under a pandemic of severe acute respiratory syndrome coronavirus 2 (SARS‑CoV‑2), responsible for coronavirus disease 2019 (COVID‑19). This disease is characterized by a respiratory syndrome that can progress to an acute respiratory distress syndrome. To date, limited effective therapies are available for the prevention or treatment of COVID‑19; therefore, it is necessary to propose novel treatment options with immunomodulatory effects. Vitamin D serves functions in bone health and has been recently reported to exert protective effects against respiratory infections. Observational studies have demonstrated an association between vitamin D deficiency and a poor prognosis of COVID‑19; this is alarming as vitamin D deficiency is a global health problem. In Latin America, the prevalence of vitamin D deficiency is unknown, and currently, this region is in the top 10 according to the number of confirmed COVID‑19 cases. Supplementation with vitamin D may be a useful adjunctive treatment for the prevention of COVID‑19 complications. The present review provides an overview of the current knowledge of the potential immunomodulatory effects of vitamin D in the prevention of COVID‑19 and sets out vitamin D recommendations for the Latin American population.

1. Introduction

Coronaviruses (CoVs) belong to one of the four genera of the Coronaviridae family characterized by a positive-sense single-stranded RNA genome of ~30 kb (1). Previously, CoVs were considered serious pathogens in animals with low influence on human health (1-3). However, at the beginning of the 21st century, the outbreak of the severe acute respiratory syndrome (SARS)-CoV emerged, followed by the Middle East respiratory syndrome (MERS)-CoV a decade later, confirming the animal-to-human and human-to-human transmission of CoVs (1,4,5). Currently, the world is under a pandemic of the third wave of CoV, initially identified as 2019-novel CoV that emerged in December 2019 in Wuhan, Hubei Province, China (6); following phylogeny analysis and taxonomy, and based on the established naming practice for viruses in this genus, the Coronaviridae Study Group of the International Committee on Taxonomy Viruses termed the novel virus SARS-CoV-2 (7). Subsequently, on February 11, 2020, the World Health Organization (WHO) reported that the disease caused by SARS-CoV-2 would be named coronavirus disease 2019 (COVID-19) (8). This disease is characterized by a respiratory syndrome that can progress to severe interstitial pneumonia and acute respiratory distress syndrome (ARDS) (9-11). The causative agent of COVID-19, SARS-CoV-2, is transmitted mainly between individuals through contact, respiratory droplets and aerosols, allowing the virus to spread rapidly (8,12). The transmission rate of SARS-CoV-2 has been reported to be higher compared with that of SARS-CoV (rq=5.7 vs. ~3.0) (13,14). The mechanism of infection of SARS-CoV-2 involves the spike protein of SARS-CoV-2 binding to the angiotensin-converting enzyme 2 (ACE2) in the host lung epithelial cells to enter the cell and initiate infection (15,16). ACE2 expression levels are high in the intestine, heart, and kidneys; therefore, this virus compromises various organs (17).

The outbreak and rapid spread of SARS-CoV-2 are a health threat with unprecedented consequences worldwide. On August 3, 2020, the Johns Hopkins University dashboard reported 18,282,208 confirmed cases and 693,694 deaths worldwide due to COVID-19 (18). On the same date, five Latin American countries (Brazil, Mexico, Peru, Chile and Colombia) were among the top 10 countries with the highest number of confirmed cases, and three countries in this region (Brazil, Mexico and Peru) were in the top 10 countries with the highest number of deaths (18). To date, various factors have been identified as predisposing for an aggressive phenotype of COVID-19, including the male sex, age >65 years, smoking and comorbidities such as diabetes, hypertension and cardiovascular disease (19). The majority of these comorbidities are associated with a sedentary lifestyle and an unhealthy diet that is commonly characterized by a high intake of saturated fats, salt, sugars, refined grains and processed meats (20,21).

A healthy diet is characterized by appropriate consumption of macronutrients and micronutrients, and is necessary for growth, development and adequate physiological functioning (21). Nutrition is also essential for the function of the immune system; this relationship is currently being studied. Particularly, it has been reported that the Mediterranean diet, as well as nutrients and active food components can modulate the immune response through the inhibition of pro-inflammatory mediators, production of anti-inflammatory functions and participation in the communication between the innate and adaptive immune system (22). For example, the Mediterranean diet (23), vitamin D (24), and polyunsaturated fatty acids (PUFAs) (25) have demonstrated promising effects on chronic inflammation and autoimmune diseases, whereas vitamin E (26), zinc (27) and probiotics (28) exhibit effects in reducing infections. Immunonutrition is defined as the provision of nutrients in amounts greater than those typically recommended in a diet that modulates the immune system activity; immunonutrients include amino acids, PUFAs, short-chain fatty acids, vitamins and trace elements (29,30). In particular, vitamin D is a crucial immunonutrient that can be obtained through the diet; however, it is produced mostly (80%) endogenously by induction of ultraviolet-B (UV-B) rays in the skin (31). Although the primary function of vitamin D appears to be calcium homeostasis, this vitamin also serves immunomodulatory functions and may have protective effects against respiratory infections (32).

Vitamin D deficiency is considered a public health problem worldwide; it is estimated that one billion individuals are deficient in vitamin D, and that insufficiency affects ~50% of the population (33). Various factors influence vitamin D deficiency, such as age, geographic latitude and skin pigmentation (34). In Latin American countries, vitamin D insufficiency has been suggested to be a potential public health problem; however, no representative data are available from this region, and the magnitude of the problem cannot be established (35).

Based on the aforementioned information, the restoration of adequate serum levels of vitamin D through supplementation has demonstrated a protective effect against respiratory infections (32). In addition, considering the lack of effective therapies for the prevention and treatment of COVID-19, it is essential to propose novel therapeutic options. Therefore, the present review aims to overview the potential immunomodulatory effects of vitamin D in the prevention of COVID-19 and to establish guideline recommendations for vitamin D supplementation for the Latin American population.

2. SARS-CoV-2 infection

Until late December 2019, only six CoV species had been identified with implications for human health, of which four (229E, OC43, NL63, and HKU1) can cause mild symptoms such as the common cold (6). Currently, SARS-CoV-2, in addition to the other two remaining CoV strains (SARS-CoV and MERS-CoV), can cause fatal outcomes (6). The genome of SARS-CoV-2 shares 79% similarity with that of SARS-CoV (36). The CoV genome encodes four main proteins: Spike, membrane, nucleocapsid and envelope (1,9). The spike protein of the virus is responsible for the viral entry to the host cells by recognizing and binding to the ACE2 receptor, which is highly expressed in various types of cells, including type II alveolar and myocardial cells, as well as the proximal tubule cells of the kidney (17,37,38). The virus spike protein binding with the ACE2 receptor is proteolytically processed by the transmembrane serine protease 2, which causes the cleavage of ACE2 and the activation of the virus spike protein to facilitate its entry to the target cell (16,39). Once inside the cell, the viral RNA genome is released into the cytoplasm to begin its replication process (40).

ARDS is one of the features of the severe COVID-19 as the virus can negatively regulate the expression of ACE2, causing the upregulation of angiotensin II (Ang II), which interacts with the Ang II type 1 receptor (AT1R) to modulate the nuclear factor-KB (NF-KB) signaling pathway, as well as macrophage activation that leads to the excessive production of pro-inflammatory cytokines (41). This exacerbated cytokine production is commonly referred to as a cytokine storm, which, in addition to contributing to ARDS, triggers a pathogenic inflammatory immune response that leads to multiple organ failure and death in severe COVID-19 (41-43).

3. Latin America: A vulnerable region

On March 11, 2020, the WHO classified COVID-19 as a pandemic due to the alarming worldwide spread of the virus and governments' inaction to prevent infection (8). A number of Latin American countries are currently among the countries with the highest number of confirmed cases and deaths associated with COVID-19 (18). Vulnerability to COVID-19 in Latin America is caused by various factors such as precarious health systems, housing conditions, high rates of non-communicable diseases, income inequality, and poverty levels (44,45). Although some countries in this region have already started vaccinating their population (Costa Rica, Argentina, Mexico, and Chile) (46), accessibility and individual factors (socioeconomic, education, religious and cultural) may affect vaccine coverage (47).

Clinical trials have been conducted to identify a treatment for COVID-19; however, limited effective therapies are available for the prevention or treatment of this disease (48-52). Furthermore, despite the current availability of vaccines, their distribution may not be equitable since during the 2009 H1N1 swine flu pandemic, countries with the highest economic position left the poorer countries with limited supplies (53,54). In addition, although health services in Latin America have notably improved since 1950, there are still deficiencies and inequity in health care (55). Therefore, it is important to propose host-directed therapeutic alternatives of easy access such as immunonutrients that may modulate the immune response to minimize the mortality rate of SARS-CoV-2 infection until a universal and effective solution is identified (56). One of the immunonutrients that has received the most interest is vitamin D; the sufficiency in serum levels of this vitamin in individuals may lead to a less severe course of COVID-19 and a faster recovery compared with that in individuals with vitamin D deficiency by helping prevent the cytokine storm, as well as ARDS, which is one of the leading causes of mortality among patients infected with SARS-CoV-2 (57).

4. Vitamin D

V itamin D is a fat-soluble vitamin present in two main isoforms; vitamin D2 (ergocalciferol) which is mainly present in mushrooms, and vitamin D3 (cholecalciferol), which is abundant in fish, egg yolk and liver (58). Chylomicrons support intestinal absorption of both vitamin D isoforms; however, vitamin D3 is more easily absorbed compared with vitamin D2 (33,58). However, achieving the recommended vitamin D dose from food sources may be impossible for a large part of the population (31,58).

As aforementioned, the major source of vitamin D for physiological functions is through synthesis in the epidermis from a cholesterol precursor (7-dehydrocholesterol) following exposure to UV-B radiation (290-320 nm) from the sun (31,59). This process induces to the formation of pre-vitamin D3, which isomerizes to vitamin D3 in a thermo-sensitive process (60). Dietary or skin-synthesized vitamin D3 binds to the vitamin D-binding protein (DBP), which transports it to the liver, where it is metabolized mainly by the enzyme vitamin D-25-hydroxylase to form calcidiol, also termed 25-hydroxyvitamin D [25(OH)D] (59). Subsequently, 25(OH)D is transformed in the kidneys by cytochrome P450 family 27 subfamily B member 1 (CYP27B1, also termed 25-hydroxyvitamin D-1α-hydroxylase) to obtain 1,25-dihydroxyvitamin D [1,25(OH)2D], also termed calcitriol, which is the main active form of vitamin D responsible for its physiological functions (59,60). In the regulation of calcitriol production, parathyroid hormone (PTH) has the ability to stimulate renal calcitriol production by activating CYP27B1, whereas fibroblast growth factor 23 (FGF-23) and calcitriol itself inhibit CYP27B1 (60,61). Similarly, high serum calcium and calcitriol concentrations inhibit CYP27B1 indirectly by suppressing PTH, and high serum phosphate concentration suppresses renal calcitriol production through the stimulation of FGF-23 (61). Excess 1,25(OH)2D is excreted through the bile or urine as calcitroic acid (Fig. 1) (31,62).

Calcitriol exerts its genomic functions through the vitamin D receptor (VDR), which acts as a transcription factor that forms a complex with the retinoid-X receptor (RXR); this complex recruits transcriptional coactivators or corepressors to regulate gene transcription by binding to vitamin D response elements (VDREs) in the DNA (59,60). In addition to the endocrine function of calcitriol in regulating calcium levels for bone remodeling, extrarenal hydroxylation occurs to form calcitriol, exerting paracrine and autocrine effects (61,63). Extrarenal hydroxylation by CYP27B1 occurs in the prostate, brain, placenta, lungs and immune cells (63). In particular, VDR activation by locally produced calcitriol has been reported to mediate the immune response (62-64), as discussed in the following sections.

5. Vitamin D and respiratory infection

Among the most common viruses that affect human health through respiratory tract infections are influenza viruses, classified into four types. Influenza type A is the most common in seasonal epidemics and pandemics, and is the primary cause of a severe illness that is associated with high mortality rates in high-risk populations (adults >65 years, individuals with chronic diseases or immunosuppression, pregnant women, individuals with obesity and infants ≤6 months) (65). The influenza viruses exhibit typical winter infection peaks in temperate zones (66), which correspond to November to April and May to October in the northern and southern hemisphere, respectively (65). By contrast, in tropical zones, the seasonality of influenza infections appears to be poorly defined, although it is assumed that it can occur throughout the year (65,67).

In 1981, Hope-Simpson (68) was the first to describe the association between influenza infection peaks and temperate latitudes in the winter. He proposed the existence of a seasonal stimulus associated with the seasonality of epidemic influenza, and that the decrease in solar radiation during winter influenced the presence of the seasonal stimulus. The study also suggested that, in the tropical regions, although UV-B radiation is less seasonal, influenza outbreaks are more severe during the rainy seasons. Thus, Hope-Simpson described that latitude determined the time of epidemics in the annual cycle, since solar radiation may act positively or negatively on the virus, the host or their interaction (68). After >20 years, Cannell et al (69) proposed that vitamin D was a likely candidate to be the seasonal stimulus described by Hope-Simpson. Since vitamin D3 is obtained by sun exposure, the serum levels of 25(OH)D are lower in people who live in temperate latitudes, and because vitamin D has modulating effects on the immune system (69).

Based on the aforementioned theories, it has been reported that the levels of UV-B radiation in countries outside the 40° N and 40° S latitude range are insufficient to produce vitamin D in the skin during winter (70). The average concentration of 25(OH)D in European countries during winter has been reported to be 11.6 ng/ml (29 nmol/l) (71), 14.3 ng/ml (35.75 nmol/l) (72) and 13.3 ng/ml (33.25 nmol/l) (73). Similarly, in the northern and central regions of the United States of America, the concentration of 25(OH)D during winter is ~21 ng/ml (52.5 nmol/l), whereas in the summer, it is ~28 ng/ml (70 nmol/l) (74). Canada has reported that between December and January (winter), there is a peak in the prevalence of 25(OH)D insufficiency/deficiency in its population (75). Although the influence of solar radiation on vitamin D deficiency is evident, several additional factors impact its deficiency, which will be discussed in subsequent sections. These factors can also affect the tropical zone population, such as that in Latin America, although the intensity of the sun rays in this region is greater (70). Other factors associated with the seasonality of respiratory infections include the congregation indoors during winter, which increases the probability of contagion, as well as the cold and dry conditions that contribute to the influenza transmission (69,76,77). A recent meta-analysis of 14 observational studies has reported that a low serum concentration of 25(OH)D is a risk factor for acute respiratory tract infection (OR=1.83; 95% CI, 1.42-2.37; P-value for heterogeneity, <0.001) (78). Similarly, in a sub-analysis of four studies, a low serum concentration of 25(OH)D was associated with high mortality from acute respiratory tract infection (OR=3.00; 95% CI, 1.89-4.78; P-value for heterogeneity, 0.029). Notably, the funnel plot in the aforementioned study identified evidence of publication bias (78). By contrast, a meta-analysis of 25 randomized controlled trials has reported that vitamin D supplementation is associated with a lower risk of acute respiratory tract infections (OR=0.88; 95% CI, 0.81-0.96; P=0.003; P-value for heterogeneity, <0.001) (32).

6. Vitamin D and COVID-19

CoVs cause respiratory infections ranging from the common cold to severe conditions such as pneumonia and ARDS (1,6,10). Therefore, the immunoregulatory effects of vitamin D are being discussed due to its potential beneficial effects for clinical outcomes in SARS-CoV-2 infection. In the international platforms for the registration of clinical trials, a number of studies evaluating the effects of vitamin D supplementation on COVID-19 have been registered, although the majority of these studies have not yet reported any results. Despite this temporal limitation, numerous studies support the association between vitamin D and the clinical outcomes of COVID-19.

Among the observational studies published in the first semester of 2020, significant associations were reported between latitudes and mortality from COVID-19, as well as between 25(OH)D deficiency and SARS-CoV-2 infection (57,79-84). These studies are summarized in Table I.

Table I

Observational studies of the association between vitamin D and COVID-19.

Table I

Observational studies of the association between vitamin D and COVID-19.

First author, yearStudy designSubjects or countriesMain outcomeConclusion(Refs.)
Rhodes et al, 2020Ecological120 countriesCorrelation of latitude degrees with mortality from COVID-19 per million in different countries: rho=0.53; P≤0.0001Mortality per million is higher in countries with a latitude above 35° n; above this latitude, people do not receive sufficient sunlight to retain adequate vitamin D levels during winter(57)
Ilie et al, 2020Ecological20 countriesCorrelation of mortality from COVID-19 per million with a mean 25(OH)D concentration in different countries: r=-0.43; P=0.05The association may explain the possible protection of vitamin D from the negative consequences of SARS-CoV-2 infection(79)
Hastie et al, 2020Ecological1,474 subjectsAssociation of 25(OH)D concentration with positive COVID-19: OR=1.00; 95% CI, 0.998-1.01; P=0.208The results do not support the potential of 25(OH)D concentration for susceptibility to COVID-19 infection(80)
D'Avolio et al, 2020Retrospective107 subjectsDifference of 25(OH)D concentration in the positive and negative SARS-CoV-2 groups: 11.1 ng/mla (IQR, 8.2-21.0) vs. 24.6 ng/mla (IQR, 8.9-30.5); P=0.004Low concentration of 25(OH)D may represent a risk factor for infection with SARS-CoV-2(81)
Meltzer et al, 2020Retrospective499 subjectsAssociation of 25(OH)D deficiency with a positive test for COVID-19: RR=1.77; P=0.015Individuals with vitamin D deficiency have a higher risk of a positive test for COVID-19 compared with those with sufficiency(82)
Whittemore, 2020Ecological88 countriesCorrelation of latitude with death rates per million from COVID-19 in different countries: r=0.40; P≤0.00005Mortality per million is lower in populations closest to the Equator. The correlation supports a possible association between latitude, sunlight exposure, vitamin D and COVID-19 mortality(83)
Panagiotou et al, 2020retrospective134 subjectsDifference in the prevalence of 25(OH)D sufficiency between ICU and non-ICU patients: 19 vs. 39.1%; P=0.0225(OH)D deficiency was more prevalent in patients who required admission to the ICu than those who only needed management in medical wards; therefore, vitamin D could be a determinant of the severity of the disease. There was no significant association between 25(OH)D concentration and mortality(84)

a Median. rho, Spearman's correlation coefficient; r, Pearson's correlation coefficient; IQR, interquartile range; 25(OH)D, 25-hydroxyvitamin D; COVID-19, coronavirus disease 2019; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; ICU, intensive care unit. 1 ng/ml=2.5 nmol/l.

Studies from the second half of 2020 that include observational, quasi-experimental studies and clinical trials have also reported valuable information on the association between vitamin D and COVID-19. A number of these studies are described below.

Merzon et al (85) evaluated the association between low levels of 25(OH)D and the risk of infection by COVID-19 through an ecological study (secondary data analysis from population databases). The mean serum of 25(OH)D concentration was lower in the positive compared with the negative COVID-19 cases (P=0.026). In addition, an association was demonstrated between 25(OH)D <30 ng/ml (<75 nmol/l) and the risk of infection by SARS-CoV-2. Therefore, it was concluded that suboptimal plasma levels of 25(OH)D may be a potential risk factor for COVID-19. Another study identified that the GT rs7041 genotype of the DBP gene may confer susceptibility to COVID-19, whereas the TT rs7041 genotype may exert a protective effect (86). The authors of the aforementioned study considered that polymorphisms in the DBP gene may alter the affinity of DBP for vitamin D metabolites, which may affect COVID-19 prevalence and mortality.

In a retrospective study, Carpagnano et al (87) reported that patients with 25(OH)D concentration <10 ng/ml (25 nmol/l) had a 50% probability of mortality, whereas the risk for those with a concentration >10 ng/ml was only 5% (P=0.019). Therefore, the authors concluded that vitamin D deficiency may be a risk factor for mortality in patients with COVID-19 (87). Similar results were obtained in other studies, which reported that vitamin D deficiency significantly increased the risk of mortality from COVID-19 (88,89). By contrast, Ling et al (90) reported no significant association between serum concentrations of 25(OH)D and COVID-19 mortality. However, multivariate analysis revealed that treatment with high-dose vitamin D3 booster therapy reduced the risk of mortality (90). Therefore, Ling et al (90) consider that vitamin D3, due to its low cost, may be a potential therapeutic option for COVID-19 worldwide.

A cross-sectional study reported vitamin D deficiency (<12 ng/ml; <30 nmol/l) in 15.6% of the samples from individuals with symptoms suggestive of COVID-19, and the presence of antibodies to the SARS-CoV-2 virus was higher in subjects with vitamin D deficiency compared with that in individuals with higher levels of 25(OH)D (P=0.003) (91). In addition, vitamin D deficiency was identified as an independent factor for seropositivity to SARS-CoV-2 in subjects with COVID-19 symptoms (91). Therefore, Faniyi et al (91) conclude that supplementation with vitamin D may be an adequate therapeutic strategy for preventing or alleviating COVID-19.

In a case-control study by Ye et al (92), it was reported that patients with COVID-19 presented with lower levels of 25(OH)D compared with those in healthy control subjects (P<0.05). A subsequent sub-group analysis comparing mild and severe COVID-19 cases identified a significant association between vitamin D deficiency and COVID-19 severity (92).

A prospective cohort study comparing asymptomatic individuals (group A) vs. patients with severe COVID-19 (group B) reported a lower concentration of 25(OH)D in group B (P=0.0001). The incidence of vitamin D deficiency (<20 ng/ml; <50 nmol/l) and mortality were higher in group B compared with those in group A (93). In a sub-analysis, patients with 25(OH)D concentration <20 ng/ml (50 nmol/l) presented with significantly higher serum concentrations of IL-6 (P=0.0300) and ferritin (P=0.0003) compared with those in patients with a concentration ≥20 ng/ml; thus, the authors concluded that vitamin D deficiency may increase the inflammatory status and the possibility of a severe COVID-19 phenotype (93). By contrast, another prospective cohort study (94) reported no associations between vitamin D deficiency and clinical features of patients with COVID-19; however, the authors suggested that this result may be due to the evaluated population mainly comprising comorbid elderly patients.

In a quasi-experimental study by Annweiler et al (95), 66 elderly patients (mean age, 87.7+9.0 years) with COVID-19 residing in a nursing home were evaluated. The intervention group included patients who received an oral bolus of 80,000 IU (2,000 ^g) vitamin D3 as part of the routine maintenance treatment; the control group did not receive vitamin D3 supplementation. The results demonstrated that vitamin D3 had a protective effect on mortality, as the survival analysis revealed a shorter survival time among residents who did not receive vitamin D supplementation (P=0.002). Similar results were reported in another quasi-experimental study by Annweiler et al (96). Additionally, it was suggested that long-term regular vitamin D supplementation may protect against infections such as SARS-CoV-2 more effectively compared with oral bolus administered after COVID-19 diagnosis (96).

An open-label clinical trial evaluated whether calcifediol treatment may reduce the need for admission of patients with COVID-19 to the intensive care unit (ICU) (97). The intervention group received calcifediol and standard treatment (azithromycin and hydroxychloroquine); the control group only received the standard treatment. The patients were followed-up until they were admitted to the ICU, discharged or succumbed to the disease. The probability of admission to the ICU was significantly lower in the intervention group (2%) compared with that in the control group (50%) (P<0.001) (97). Therefore, Entrenas Castillo et al (97) concluded that calcifediol may improve the clinical outcome of subjects with COVID-19.

Rastogi et al (98) conducted a clinical trial to evaluate the effects of high-dose vitamin D3 on SARS-CoV-2 viral clearance. Patients with mild symptoms or asymptomatic individuals positive for SARS-CoV-2 infection and with vitamin D deficiency were randomly assigned to the intervention group to receive 60,000 IU (1,500 ^g) of vitamin D3 daily, or the control group, who received a placebo. The intervention was performed daily for 7 days. Patients who reached a concentration >50 ng/ml of 25(OH)D received only one additional dose of 60,000 IU, whereas those who did not reach the desired 25(OH)D levels received the same daily dose until day 14. The patients were evaluated periodically until day 21 or virus negativity. In the intervention group, ~63% of the subjects had a negative result for SARS-CoV-2, whereas only 20.8% of those in the control group had this outcome (P=0.018). In addition, the intervention group presented with a more pronounced decrease in fibrinogen levels compared with that in the control group (P=0.001). No episodes of hypercalcemia were observed in the evaluated population (98). Therefore, Rastogi et al (98) considered that vitamin D may reduce the transmission rates of SARS-CoV-2 infection.

A recent meta-analysis has reported that insufficient vitamin D levels increase the rates of hospitalization and mortality among patients with COVID-19 (99). Severe cases have a higher probability of vitamin D deficiency (OR=1.64; 95% CI, 1.30-2.09; I2=35.7%). Thus, vitamin D intervention as an adjunctive treatment may be crucial in severe cases of COVID-19 with low 25(OH)D levels. Similarly, supplementation in therapeutic doses may be useful for the prevention of SARS-CoV-2 infection, according to D'Avolio et al (81), Meltzer et al (82), Merzon et al (85) and Faniyi et al (91), since the active metabolite of vitamin D exerts biological activities in the innate immune system, in particular, through the maintenance of the integrity of physical barriers and the promotion of antimicrobial peptides (64). In addition, another meta-analysis has reported an association between low 25(OH)D levels and the risk of SARS-CoV-2 infection (OR=1.43; 95% CI, 1.00-2.05) (100). However, these results should be interpreted with caution due to the heterogeneity of the included studies (I2=64.9%; P=0.036) and the risk of publication bias. Finally, according to the meta-analysis by Martineau et al (32), vitamin D supplementation did not significantly affect any types of adverse events. However, the individual recommendatios of vitamin D3 for preventive or adjuvant treatment should be evaluated by a physician. Similarly, a consensus is considered necessary to propose public health policies for supplementation with this vitamin in risk groups.

7. Immunomodulatory mechanisms of vitamin D

As aforementioned, vitamin D in its active form [1,25(OH)2D or calcitriol] binds to the VDR and RXR to regulate gene transcription. The classic functions of vitamin D are the regulation of calcium absorption, homeostasis, bone metabolism, cell growth and division (61). In addition, VDR is expressed in immune cells such as macrophages, dendritic cells (Dcs), B and T lymphocytes, and neutrophils, suggesting that vitamin D may be an important regulator of the immune system (101,102).

Physical barriers

Physical barriers are the first line of defense against infection. Currently, the prevention and treatment of diseases focus on the preservation and restoration of the proper functioning of epithelial cells (103). In the pulmonary epithelium, the severity of acute lung injury is associated with its barrier dysfunction (104). To maintain the integrity of the alveolar wall, which forms a physical barrier against the external environment, the integrity of tight junctions (TJs) and adherens junctions (AJs) between the alveolar epithelial cells is essential (105). Epithelial TJs create a barrier that regulates the paracellular permeability of small molecules (106). The composition of TJs includes occludin, claudins and zonula occludens (ZO) proteins (105). AJs mainly comprise transmembrane proteins such as E-cadherin, as well as intracellular components (β-catenin and a-catenin), which regulate the adhesion of cells to their neighbors (105,106). A recent study has reported that in VDR−/− mice, the mRNA levels of claudins 2, 4, 10, 12, 15, and 18, as well as the protein levels of claudins 2, 4, 12, and 18 were significantly decreased compared with those in wild-type (WT) mice (107). In addition, another study reported a significant decrease in mRNA and protein levels of ZO-1 and occludin in VDR−/− compared with WT mice (108). In both studies, VDR−/− mice exhibited significant increases in the levels of inflammatory mediators compared with those in WT mice; therefore, these results suggest that VDR may serve a crucial role in maintaining lung permeability (Fig. 2A) (107,108).

Innate immunity

The innate immune response is responsible for the early recognition of invading pathogens to prevent infection (109). This action is mainly carried out by pathogen-recognition receptors, among which the Toll-like receptors (TLRs) are prominent (110). In monocytes, the heterodimer TLR2/1 interaction with pathogens induces antimicrobial peptides such as β-defensins and human cathelicidin (LL-37), as well as the activation of autophagy and phagolysosomal fusion (109,110). These antimicrobial peptides neutralize infection by disturbing the pathogen membrane homeostasis and promoting autophagy (109,111). Cathelicidin and autophagy complement each other to enhance pathogen clearance (110). TLR activation induces the expression of CYP27B1 and VDR in monocytes; subsequently, locally produced 1,25(OH)2D exerts its function through VDRs to upregulate the expression of p-defensins and LL-37 (112). This mechanism can also occur in epithelial cells of the intestine and the lungs, as well as in keratinocytes (111,113,114). By contrast, it has been reported that the induction of cathelicidin in lung epithelial cells is independent of TLRs (111). Previous studies have demonstrated that the antimicrobial activity of the innate immune response is partially dependent on vitamin D levels (Fig. 2B) (115-117).

Calcitriol can also alter the functioning of antigen-presenting cells, which are responsible for the initiation of the adaptive immune response. In particular, it has been described that 1,25(OH)2D can preserve an immature phenotype of DCs by reducing the expression of MHC class II molecules, as well as co-stimulatory molecules (CD80, CD86), which also results in a decline of IL-12 secretion (Fig. 2C) (118-121).

Adaptive immunity

Vitamin D also exerts immunomodulatory effects on the adaptive immune response. Calcitriol has been reported to suppress the activity of type 1 T-helper (Th1) cells, achieving the repression of pro-inflammatory cytokine production, including IL-2 and IFNγ (111). The repression of IL-2 production is mediated by the 1,25(OH)2D-VDR-RXR complex, which blocks the formation of the nuclear factor of activated T-cells (NFAT) and activator protein 1 complex (122). The 1,25(OH)2D-VDR-RXR complex binds to the IL-2 promoter to interrupt the function of NFAT (111). By contrast, it has been reported that 1,25(OH)2D-VDR-RXR binds to the IFNy promoter to interfere with its activation (123). In addition, calcitriol affects the regulation of IL-17 in Th17 cells (124). Although its mechanism is not yet fully understood, it has been suggested that 1,25(OH)2D inhibits the master regulator of Th17 cells. Additionally, the 1,25(OH)2D-VDR-RXR complex competes with NFAT for the IL-17A promoter; once the complex is bound, it recruits histone deacetylases to limit the transcription of this cytokine (124-126). Calcitriol has also been demonstrated to inhibit NF-κB via upregulation of IκB expression or by interfering with the binding of NF-κB to DNA (Fig. 2D) (127-129).

By contrast, vitamin D favors the differentiation of Th2 cells and the subsequent production of anti-inflammatory cytokines IL-4, IL-5 and IL-13 (130,131). 1,25(OH)2D upregulates GATA-binding protein 3 (GATA3), which is recognized as the master regulator of Th2 cells (130,132). This upregulation is mediated by the activation of STAT6, which acts upstream of GATA3 transcription (109,130,133). In addition, vitamin D increases the differentiation of regulatory T cells (Tregs) through the upregulation of the transcription factor FOXP3 and CTLA-4 expression; Treg differentiation contributes to the production of anti-inflammatory cytokines, such as IL-10 (Fig. 2D) (125,134-136).

Renin-angiotensin system

The renin-angiotensin system (RAS) comprises renin, angiotensinogen (ANG), Ang I, Ang-converting enzyme (ACE) and Ang II (41,137). This system acts as a cascade where renin degrades ANG to produce Ang I; subsequently, the ACE transforms Ang I to II (138). Ang II regulates blood pressure and electrolyte balance (137). As aforementioned, the maintained interaction of Ang II with AT1R contributes to the production of pro-inflammatory cytokines by activating NF-κB and macrophages (41). The crucial role of ACE2 in this cascade is its ability to maintain a balance, since ACE2 degrades Ang II to produce Ang (1-7) with vasodilator, antiproliferative, antithrombotic and anti-inflammatory effects (139). However, in SARS-CoV-2 infection, a negative regulation of ACE2 has been demonstrated, which leads to the subsequent cytokine storm and, therefore, severe COVID-19 (41,139).

1,25(OH)2D has been reported to be an essential regulator of RAS since it suppresses the activity of renin; although the underlying mechanism is currently unclear, it has been suggested that 1,25(OH)2D suppresses renin expression by blocking the binding of the cAMP response element-binding protein with its response elements in the renin gene promoter (Fig. 2E) (140-142).

8. Causes of vitamin D deficiency

Vitamin D insufficiency affects ~50% of the world's population. The high prevalence of this vitamin insufficiency is considered a public health problem (33), since hypovitaminosis D has been identified as an independent risk factor for all-cause mortality in the general population (143). Vitamin D is commonly referred to as the 'sunshine vitamin', as most of the endogenous vitamin D is synthesized during exposure to solar UV-B rays, which causes the formation of vitamin D3 in the skin (33,70). Therefore, its deficiency is generally attributed to latitude or insufficient solar radiation; however, several additional factors contribute to low serum levels of 25(OH)D, which is a reliable marker of vitamin D status (144). These additional factors that predispose individuals to vitamin D deficiency impact tropical countries despite sufficient solar radiation intensity (70). For example, skin pigmentation and the use of sunscreens affect the synthesis of vitamin D3 in the skin (145-147), low vitamin D intake and obesity decrease the bioavailability of 25(OH)D (58,148), whereas liver failure and nephrotic syndrome alter its synthesis and excretion, respectively (149-151). Similarly, certain factors impact the catabolism and synthesis of 1,25(OH)D (152-156). These and other factors are described in detail in Table II (157-162).

Table II

Causes of vitamin D deficiency.

Table II

Causes of vitamin D deficiency.

CauseEffect(Refs.)
Reduced synthesis in the skin
Sunscreen: Use of sunscreens to prevent sunburn and skin cancer
Skin pigmentation: Melanin reduces the penetration of UV-B rays
Time of day: The more oblique the zenith angle, the fewer UV-B photons reach the Earth's surface
Aging: Decreased concentration of 7-dehydrocholesterol in the epidermis
Other factors: Clothing habits, cloud cover, pollution, season and latitude
May reduce vitamin D3 synthesis under strictly controlled conditions
Reduced effectiveness of vitamin D3 synthesis in the skin
The production of vitamin D3 in the skin is absent in the early hours or late in the day 50% decrease in vitamin D3 production in old age
Decrease or absence of vitamin D3 synthesis in the skin
(145-147,159,160)
Decreased bioavailability
Diet: Limited intake of natural and fortified foods with vitamin D, lack of supplementation
Malabsorption: Intestinal malabsorption syndromes (cystic fibrosis, celiac disease, inflammatory bowel disease and short bowel syndrome); bile acid sequestrants (colestipol and cholestyramine) and lipase inhibitors (orlistat)
Obesity: Volumetric dilution of vitamin D in the compartments that are increased in obesity (serum, muscle, liver and adipose tissue)
Decreased bioavailability of 25(OH)D
Decreased ability to absorb vitamin D
Decreased bioavailability of 25(OH)D
(58,148,161,162)
Increased catabolism
Drugs: Glucocorticoid and antiepileptic treatment
1,25(OH)2D degradation due to increased
24-OHase activity. These drugs may increase the expression of 24-OHase through the activation of the pregnane X receptor
(152-154)
Decreased synthesis of 25(OH)D
Liver failure: Chronic liver disease
Decreased hydroxylation of vitamin D resulting in low levels of 25(OH)D(149)
Increased urinary loss of 25(OH)D
Nephrotic syndrome: 25(OH)D bound to DBP is lost in the urine
Significant loss of 25(OH)D in urine due to proteinuria(150,151)
Decreased synthesis of 1,25(OH)2D
Chronic kidney disease: Decreased renal mass limits the amount of CYP27B1; decreased glomerular filtration rate may limit delivery of substrate to the CYP27B1
Progressive decrease in 1,25(OH)2D during the course of kidney disease(155,156)
Genetic polymorphisms
Single nucleotide polymorphisms at DHCR7 (rs7944926), GC (rs2282679), CYP2R1 (rs10741657), CYP27B1 (rs10877012) and VDR (rs2228570)
Low serum 25(OH)D concentrations and less effective transcriptional activation of VDR(157,158)

[i] Adapted from ref. (62). UV-B, ultraviolet-B; 25(OH)D, 25-hydroxyvitamin D; 1,25(OH)2D, 1,25-dihydroxyvitamin D; 24-OHase, 25-hydroxyvitamin D-24-hydroxylase; DBP, vitamin D-binding protein; VDR, vitamin D receptor.

9. Vitamin D deficiency in Latin America: A paradox of the tropical zone

As aforementioned, in addition to latitude, various factors influence vitamin D levels in the human body (62). Therefore, the Latin American population, the vast majority of which resides in the tropical zone, is not exempt from vitamin D deficiency (70). Vitamin D insufficiency in this region may be a public health problem; however, despite studies that report 25(OH)D deficiencies in the Latin American population, it is impossible to establish the magnitude of the problem due to the lack of nationally representative data (35). Table III summarizes the most recent reports on the status of 25(OH)D in the population of Latin American countries that are among the top 10 countries by confirmed cases and deaths from COVID-19 globally (18,163-167). Although the definition of serum 25(OH)D status varies among the studies, the majority of these reports align with the recommendations of the Institute of Medicine (IOM) (168) and the Endocrine Society (169): Vitamin D deficiency is defined as serum levels of 25(OH)D <20 ng/ml (<50 nmol/l), and vitamin D insufficiency is defined as serum levels between 21 ng/ml (52.5 nmol/l) and 29 ng/ml (72.5 nmol/l). Of note, the IOM suggests that 25(OH)D levels >20 ng/ml (>50 nmol/l) are sufficient to meet the needs of ~98% of the population; however, this recommendation mainly considers the maintenance of bone health (168).

Table III

Serum concentration of 25(OH)D in some Latin American countries.

Table III

Serum concentration of 25(OH)D in some Latin American countries.

CountryAge groupAge (years)NMean 25(OH)D, ng/ml(Refs.)
BrazilAdults39.8±10.957223.2±5.9(163)
MexicoAdults57.8±16.611718.4±7.2(164)
PeruAdolescents14.9±0.81,44125.3 (rangeb, 73.1)(165)
ChileAdult women
Older women
35.4±8.5
73.6±6.6
1,245
686
20.2±8.0
18±8.5
(166)
ColombiaAdults57a (rangeb, 24.0)1,33932.3a(rangeb, 23.2)(167)

a Median.

b Difference between the minimum and maximum value; specific values are not available in the original study. 25(OH)D, 25-hydroxyvitamin D. 1 ng/ml=2.5 nmol/l.

10. Vitamin D supplementation for infection prevention

Various factors cause a high prevalence of vitamin D deficiency. However, although latitude and season are key factors, certain countries with long winters report lower rates of deficiency compared with those in countries in the tropical zone; this may be due to food fortification, high consumption of fatty fish and supplementation (170). Therefore, although the recommendations for restoring the levels of vitamin D include the consumption of foods rich in vitamin D and increased sun exposure, considering the difficulty of generalized access to foods such as fish, clothing habits and the avoidance of sunlight, supplementation may represent an effective strategy (58). Furthermore, the recommendation of vitamin D supplementation may not only help prevent low concentrations of 25(OH)D and improve bone health, but may also be useful for the prevention of complications following infection with SARS-CoV-2 (57).

Regarding the recommendations for vitamin D intake, these may vary between populations. The IOM recommends daily consumption of 600 IU (15 μg) for children >1 year and adults ≤70 years (168). Similarly, the European Food Safety Authority recommends a daily intake of 600 IU (15 μg), with a maximum intake of 4,000 IU/day (100 μg) in healthy adults (171,172). The UK Scientific Advisory Committee on Nutrition recommends vitamin D intake of 400 IU/day (10 μg) for everyone in the general population >4 years (173), whereas the European Food Safety Agency has reported that vitamin D doses of ≤10,000 IU/day (≤250 μg) are safe if there are no comorbidities (171,172). Other reports indicate that doses ≤6,000 IU/day (≤150 μg) are necessary to achieve serum 25(OH)D concentrations >40 ng/ml (100 nmol/l). Doses of ≤15,000 IU/day (≤375 μg) have also been reported to be safe and effective for rapidly increasing 25(OH)D concentrations (174). The Brazilian Society of Endocrinology and Metabology (175) and the Ministry of Health of the Government of Chile (176) adhere to the recommendations indicated by the IOM. In colombia, the colombian consensus on Vitamin D recommends an intake of ≤2,000 IU/day (≤50 μg) in cases of insufficiency, and ≤6,000 IU/day (≤150 μg) in deficiency (177). The suggested daily intake in Mexico is only 224 IU (5.6 μg), as there are currently no studies demonstrating the need to supplement vitamin D in the Mexican population (178).

Supplementation with vitamin D may be necessary for individuals with deficiency to achieve a sufficient concentration of 25(OH)D, which is >30 ng/ml (75 nmol/l), even with consumption of fortified foods, since it is difficult to maintain this concentration with food alone (179). An international consensus for the recommended daily intake for vitamin D would be useful; however, considering that vitamin D deficiency is an undoubted global problem, that there is a lack of clinical trials that accurately indicate the appropriate dose of vitamin D supplementation. Due to the need to establish accessible strategies for the prevention of complications from COVID-19, the authors of the present review agree with the current proposal of Grant et al (180), who suggested that individuals with low levels of 25(OH)D should be supplemented for a month with 10,000 IU/day (250 μg) of vitamin D3 for the rapid restoration of the desired concentrations between 40 and 60 ng/ml (100 and 150 nmol/l). For maintenance, this should be followed by daily supplementation of 5,000 IU (125 μg).

Notably, that baseline monitoring of 25(OH)D concentrations should be considered. In addition, avoiding high doses of calcium and assessing the consumption of magnesium and vitamin K2 should be considered for the prevention of long-term adverse effects of high doses of vitamin D (180,181).

11. Conclusions

The lack of effective therapies and the uncertainty of universal access to possible vaccines for COVID-19 demand alternatives with potential immunomodulatory effects such as vitamin D supplementation, which may contribute to the prevention of respiratory infections and their complications. However, it is necessary to await the results of the undergoing clinical trials and to continue with the execution of further studies to determine the effects of vitamin D supplementation on COVID-19 and establish the ideal dosage. Observational studies appear to demonstrate an association between low vitamin D concentrations and susceptibility to SARS-CoV-2 infection. However, it is also vital to carry out national and international studies to determine the prevalence of vitamin D deficiency in Latin America. The authors of the present study call on the corresponding authorities to assess the fortification with vitamin D of foods for daily consumption, since supplementation may represent a difficulty for individuals with a low income.

Funding

This research was funded by the National Council of Science and Technology (CONACYT Ciencia Básica; grant no. A1-S-8774) and Universidad de Guadalajara through the 'Fortalecimiento de la Investigatión y el Posgrado 2020' fund.

Availability of data and materials

Not applicable.

Authors' contributions

FJTH, and JFMV conceived, drafted, and finalized the manuscript. JFMV, GASZ, GGE, JHB, and GMO critically reviewed the manuscript for important intellectual content. All authors read and approved the final manuscript.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Acknowledgments

Not applicable.

References

1 

da Costa VG, Moreli ML and Saivish MV: The emergence of SARS, MERS and novel SARS-2 coronaviruses in the 21st century. Arch Virol. 165:1517–1526. 2020. View Article : Google Scholar

2 

Lee C: Porcine epidemic diarrhea virus: An emerging and re-emerging epizootic swine virus. Virol J. 12:1932015. View Article : Google Scholar : PubMed/NCBI

3 

Bande F, Arshad SS, Bejo MH, Moeini H and Omar AR: Progress and challenges toward the development of vaccines against avian infectious bronchitis. J Immunol Res. 2015:4248602015. View Article : Google Scholar : PubMed/NCBI

4 

Fouchier RA, Kuiken T, Schutten M, van Amerongen G, van Doornum GJ, van den Hoogen BG, Peiris M, Lim W, Stohr K and Osterhaus AD: Aetiology: Koch's postulates fulfilled for SARS virus. Nature. 423:2402003. View Article : Google Scholar : PubMed/NCBI

5 

Zaki AM, van Boheemen S, Bestebroer TM, Osterhaus ADME and Fouchier RAM: Isolation of a novel coronavirus from a man with pneumonia in Saudi Arabia. N Engl J Med. 367:1814–1820. 2012. View Article : Google Scholar : PubMed/NCBI

6 

Zhu N, Zhang D, Wang W, Li X, Yang B, Song J, Zhao X, Huang B, Shi W, Lu R, et al: A novel coronavirus from patients with pneumonia in China, 2019. N Engl J Med. 382:727–733. 2020. View Article : Google Scholar : PubMed/NCBI

7 

Coronaviridae Study Group of the International Committee on Taxonomy of Viruses: The species Severe acute respiratory syndrome-related coronavirus: Classifying 2019-nCoV and naming it SARS-CoV-2. Nat Microbiol. 5:536–544. 2020. View Article : Google Scholar : PubMed/NCBI

8 

World Health Organization: Timeline of WHO's response to COVID-19. 2020.

9 

Petrosillo N, Viceconte G, Ergonul O, Ippolito G and Petersen E: COVID-19, SARS and MERS: Are they closely related? Clin Microbiol Infect. 26:729–734. 2020. View Article : Google Scholar : PubMed/NCBI

10 

Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y, Qiu Y, Wang J, Liu Y, Wei Y, et al: Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: A descriptive study. Lancet. 395:507–513. 2020. View Article : Google Scholar :

11 

Liu K, Fang YY, Deng Y, Liu W, Wang MF, Ma JP, Xiao W, Wang YN, Zhong MH, Li CH, et al: Clinical characteristics of novel coronavirus cases in tertiary hospitals in Hubei Province. Chin Med J (Engl). 133:1025–1031. 2020. View Article : Google Scholar

12 

Tang S, Mao Y, Jones RM, Tan Q, Ji JS, Li N, Shen J, LV Y, Pan L, Ding P, et al: Aerosol transmission of SARS-CoV-2? Evidence, prevention and control. Environ Int. 144:1060392020. View Article : Google Scholar : PubMed/NCBI

13 

Sanche S, Lin YT, Xu C, Romero-Severson E, Hengartner N and KE R: High contagiousness and rapid spread of severe acute respiratory syndrome coronavirus 2. Emerg Infect Dis. 26:1470–1477. 2020. View Article : Google Scholar : PubMed/NCBI

14 

Bauch CT, Lloyd-Smith JO, Coffee MP and Galvani AP: Dynamically modeling SARS and other newly emerging respiratory illnesses: Past, present, and future. Epidemiology. 16:791–801. 2005. View Article : Google Scholar : PubMed/NCBI

15 

Walls AC, Park YJ, Tortorici MA, Wall A, McGuire AT and Veesler D: Structure, function, and antigenicity of the SARS-CoV-2 spike glycoprotein. Cell. 181:281–292.e6. 2020. View Article : Google Scholar :

16 

Hoffmann M, Kleine-Weber H, Schroeder S, Krüger N, Herrler T, Erichsen S, Schiergens TS, Herrler G, Wu NH, Nitsche A, et al: SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell. 181:271–280.e8. 2020. View Article : Google Scholar : PubMed/NCBI

17 

Zou X, Chen K, Zou J, Han P, Hao J and Han Z: Single-cell RNA-seq data analysis on the receptor ACE2 expression reveals the potential risk of different human organs vulnerable to 2019-nCoV infection. Front Med. 14:185–192. 2020. View Article : Google Scholar : PubMed/NCBI

18 

Johns Hopkins University Coronavirus Resource Center: COVID-19 Dashboard by the Center for Systems Science and Engineering (CSSE) at Johns Hopkins University (JHU). 2020.

19 

Zheng Z, Peng F, Xu B, Zhao J, Liu H, Peng J, Li Q, Jiang C, Zhou Y, Liu S, et al: Risk factors of critical & mortal COVID-19 cases. A systematic literature review and meta-analysis. J Infect. 81:e16–e25. 2020. View Article : Google Scholar

20 

Peters R, Ee N, Peters J, Beckett N, Booth A, Rockwood K and Anstey KJ: Common risk factors for major noncommunicable disease, a systematic overview of reviews and commentary. The implied potential for targeted risk reduction. Ther Adv Chronic Dis. Oct 15–2019.Epub ahead of print. View Article : Google Scholar

21 

Cena H and Calder PC: Defining a healthy diet: Evidence for the role of contemporary dietary patterns in health and disease. Nutrients. 12:3342020. View Article : Google Scholar :

22 

Wu D, Lewis ED, Pae M and Meydani SN: Nutritional modulation of immune function. Analysis of evidence, mechanisms, and clinical relevance. Front Immunol. 9:31602019. View Article : Google Scholar

23 

Forsyth C, Kouvari M, D'Cunha NM, Georgousopoulou EN, Panagiotakos DB, Mellor DD, Kellett J and Naumovski N: The effects of the Mediterranean diet on rheumatoid arthritis prevention and treatment. A systematic review of human prospective studies. Rheumatol Int. 38:737–747. 2018. View Article : Google Scholar

24 

Zheng R, Gonzalez A, Yue J, Wu X, Qiu M, Gui L, Zhu S and Huang L: Efficacy and safety of vitamin D supplementation in patients with systemic lupus erythematosus. A meta-analysis of randomized controlled trials. Am J Med Sci. 358:104–114. 2019. View Article : Google Scholar : PubMed/NCBI

25 

Lee KR, Midgette Y and Shah R: Fish oil derived omega 3 fatty acids suppress adipose NLRP3 inflammasome signaling in human obesity. J Endocr Soc. 3:504–515. 2018. View Article : Google Scholar

26 

Hussain MI, Ahmed W, Nasir M, Mushtaq MH, Sheikh AA, Shaheen AY and Mahmood A: Immune boosting role of vitamin E against pulmonary tuberculosis. Pak J Pharm Sci. 32(Suppl 1): S269–S276. 2019.

27 

Martinez-Estevez NS, Alvarez-Guevara AN and Rodriguez-Martinez CE: Effects of zinc supplementation in the prevention of respiratory tract infections and diarrheal disease in Colombian children. A 12-month randomised controlled trial. Allergol Immunopathol (Madr). 44:368–375. 2016. View Article : Google Scholar

28 

Zhang H, Yeh C, Jin Z, Ding L, Liu BY, Zhang L and Dannelly HK: Prospective study of probiotic supplementation results in immune stimulation and improvement of upper respiratory infection rate. Synth Syst Biotechnol. 3:113–120. 2018. View Article : Google Scholar : PubMed/NCBI

29 

McCarthy MS and Martindale RG: Immunonutrition in critical illness. What is the role? Nutr Clin Pract. 33:348–358. 2018. View Article : Google Scholar : PubMed/NCBI

30 

Chow O and Barbul A: Immunonutrition. Role in wound healing and tissue regeneration. Adv Wound Care (New Rochelle). 3:46–53. 2014. View Article : Google Scholar

31 

Pilz S, Zittermann A, Trummer C, Theiler-Schwetz V, Lerchbaum E, Keppel MH, Grübler MR, März W and Pandis M: Vitamin D testing and treatment. A narrative review of current evidence. Endocr Connect. 8:R27–R43. 2019. View Article : Google Scholar

32 

Martineau AR, Jolliffe DA, Hooper RL, Greenberg L, Aloia JF, Bergman P, Dubnov-Raz G, Esposito S, Ganmaa D, Ginde AA, et al: Vitamin D supplementation to prevent acute respiratory tract infections. Systematic review and meta-analysis of individual participant data. BMJ. 356:i65832017. View Article : Google Scholar

33 

Nair R, Maseeh A and Vitamin D: The 'sunshine' vitamin. J Pharmacol Pharmacother. 3:118–126. 2012.PubMed/NCBI

34 

Roth DE, Abrams SA, Aloia J, Bergeron G, Bourassa MW, Brown KH, Calvo MS, Cashman KD, Combs G, De-Regil LM, et al: Global prevalence and disease burden of vitamin D deficiency: A roadmap for action in low- and middle-income countries. Ann NY Acad Sci. 1430:44–79. 2018. View Article : Google Scholar : PubMed/NCBI

35 

Brito A, Cori H, Olivares M, Fernanda Mujica M, Cediel G and Lopez de Romana D: Less than adequate vitamin D status and intake in Latin America and the Caribbean. A problem of unknown magnitude. Food Nutr Bull. 34:52–64. 2013. View Article : Google Scholar : PubMed/NCBI

36 

Ren LL, Wang YM, Wu ZQ, Xiang ZC, Guo L, Xu T, Jiang YZ, Xiong Y, Li YJ, Li XW, et al: Identification of a novel coronavirus causing severe pneumonia in human: A descriptive study. Chin Med J (Engl). 133:1015–1024. 2020. View Article : Google Scholar

37 

Li W, Moore M J, Vasilieva N, Sui J, Wong S K, Berne M A, Somasundaran M, Sullivan JL, Luzuriaga K, Greenough TC, et al: Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus. Nature. 426:450–454. 2003. View Article : Google Scholar : PubMed/NCBI

38 

Jia HP, Look DC, Shi L, Hickey M, Pewe L, Netland J, Farzan M, Wohlford-Lenane C, Perlman S and McCray PB Jr: ACE2 receptor expression and severe acute respiratory syndrome coronavirus infection depend on differentiation of human airway epithelia. J Virol. 79:14614–14621. 2005. View Article : Google Scholar : PubMed/NCBI

39 

Rabi FA, Al Zoubi MS, Kasasbeh GA, Salameh DM and Al-Nasser AD: SARS-CoV-2 and coronavirus disease 2019: What we know so far. Pathogens. 9:2312020. View Article : Google Scholar :

40 

Yuki K, Fujiogi M and Koutsogiannaki S: COVID-19 pathophysiology: A review. Clin Immunol. 215:1084272020. View Article : Google Scholar : PubMed/NCBI

41 

Banu N, Panikar SS, Leal LR and Leal AR: Protective role of ACE2 and its downregulation in SARS-CoV-2 infection leading to macrophage activation syndrome: Therapeutic implications. Life Sci. 256:1179052020. View Article : Google Scholar : PubMed/NCBI

42 

Li X, Geng M, Peng Y, Meng L and Lu S: Molecular immune pathogenesis and diagnosis of COVID-19. J Pharm Anal. 10:102–108. 2020. View Article : Google Scholar : PubMed/NCBI

43 

Nile SH, Nile A, Qiu J, Li L, Jia X and Kai G: COVID-19: Pathogenesis, cytokine storm and therapeutic potential of interferons. Cytokine Growth Factor Rev. 53:66–70. 2020. View Article : Google Scholar : PubMed/NCBI

44 

Burki T: COVID-19 in Latin America. Lancet Infect Dis. 20:547–548. 2020. View Article : Google Scholar : PubMed/NCBI

45 

Bolano-Ortiz TR, Camargo-Caicedo Y, Puliafito SE, Ruggeri MF, Bolano-Diaz S, Pascual-Flores R, Saturno J, Ibarra-Espinosa S, Mayol-Bracero OL, Torres-Delgado E and Cereceda-Balic F: Spread of SARS-CoV-2 through Latin America and the Caribbean region: A look from its economic conditions, climate and air pollution indicators. Environ Res. 191:1099382020. View Article : Google Scholar : PubMed/NCBI

46 

World Health Organization: Our World in Data: Coronavirus (COVID-19) Vaccinations. 2021.

47 

Guzman-Holst A, DeAntonio R, Prado-Cohrs D and Juliao P: Barriers to vaccination in Latin America: A systematic literature review. Vaccine. 38:470–481. 2020. View Article : Google Scholar

48 

Pathak DSK, Salunke DAA, Thivari DP, Pandey A, Nandy DK, Harish VK, Ratna D, Pandey DS, Chawla DJ, Mujawar DJ, Dhanwate DA and Menon DV: No benefit of hydroxychloroquine in COVID-19: Results of systematic review and meta-analysis of randomized controlled trials'. Diabetes Metab Syndr. 14:1673–1680. 2020. View Article : Google Scholar : PubMed/NCBI

49 

Cao B, Wang Y, Wen D, Liu W, Wang J, Fan G, Ruan L, Song B, Cai Y, Wei M, et al: A trial of lopinavir-ritonavir in adults hospitalized with severe covid-19. N Engl J Med. 382:1787–1799. 2020. View Article : Google Scholar : PubMed/NCBI

50 

Novartis: Novartis provides update on CAN-COVID trial in hospitalized patients with COVID-19 pneumonia and cytokine release syndrome (CRS). 2020.

51 

Sanofi: Sanofi provides update on Kevzara® (sarilumab) Phase 3 trial in severe and critically ill COVID-19 patients outside the U.S. 2020.

52 

AstraZeneca: Update on CALAVI phase II trials for calquence in patients hospitalised with respiratory symptoms of COVID-19. 2020.

53 

Iserson KV: SARS-CoV-2 (COVID-19) vaccine development and production: An ethical way forward. Camb Q Healthc Ethics. 30:59–68. 2021. View Article : Google Scholar

54 

Bollyky TJ, Gostin LO and Hamburg MA: The equitable distribution of COVID-19 therapeutics and vaccines. JAMA. 323:2462–2463. 2020. View Article : Google Scholar : PubMed/NCBI

55 

Barreto SM, Miranda JJ, Figueroa JP, Schmidt MI, Munoz S, Kuri-Morales PP and Silva JB Jr: Epidemiology in Latin America and the Caribbean: Current situation and challenges. Int J Epidemiol. 41:557–571. 2012. View Article : Google Scholar : PubMed/NCBI

56 

Zumla A, Hui DS, Azhar EI, Memish ZA and Maeurer M: Reducing mortality from 2019-nCoV: Host-directed therapies should be an option. Lancet. 395:e35–e36. 2020. View Article : Google Scholar : PubMed/NCBI

57 

Rhodes JM, Subramanian S, Laird E and Kenny RA: Editorial: Low population mortality from COVID-19 in countries south of latitude 35 degrees North supports vitamin D as a factor determining severity. Aliment Pharmacol Ther. 51:1434–1437. 2020. View Article : Google Scholar : PubMed/NCBI

58 

Lamberg-Allardt C: Vitamin D in foods and as supplements. Prog Biophys Mol Biol. 92:33–38. 2006. View Article : Google Scholar : PubMed/NCBI

59 

Jeon SM and Shin EA: Exploring vitamin D metabolism and function in cancer. Exp Mol Med. 50:202018. View Article : Google Scholar : PubMed/NCBI

60 

Bikle DD: Vitamin D metabolism, mechanism of action, and clinical applications. Chem Biol. 21:319–329. 2014. View Article : Google Scholar : PubMed/NCBI

61 

Christakos S, Dhawan P, Verstuyf A, Verlinden L and Carmeliet G: Vitamin D: Metabolism, molecular mechanism of action, and pleiotropic effects. Physiol Rev. 96:365–408. 2016. View Article : Google Scholar :

62 

Holick MF: Vitamin D deficiency. N Engl J Med. 357:266–281. 2007. View Article : Google Scholar : PubMed/NCBI

63 

Bivona G, Agnello L and Ciaccio M: The immunological implication of the new vitamin D metabolism. Cent J Immunol. 43:331–334. 2018. View Article : Google Scholar

64 

Charoenngam N and Holick MF: Immunologic effects of vitamin d on human health and disease. Nutrients. 12:20972020. View Article : Google Scholar :

65 

Ghebrehewet S, MacPherson P and Ho A: Influenza. BMJ. 355:i62582016. View Article : Google Scholar : PubMed/NCBI

66 

Tamerius JD, Shaman J, Alonso WJ, Bloom-Feshbach K, Uejio CK, Comrie A and Viboud C: Environmental predictors of seasonal influenza epidemics across temperate and tropical climates. PLoS Pathog. 9:e10031942013. View Article : Google Scholar : PubMed/NCBI

67 

Arbeitskreis Blut, Untergruppe 'Bewertung Blutassoziierter Krankheitserreger': Influenza virus. Transfus Med Hemother. 36:32–39. 2009. View Article : Google Scholar

68 

Hope-simpson RE: The role of season in the epidemiology of influenza. J Hyg (Lond). 86:35–47. 1981. View Article : Google Scholar

69 

Cannell JJ, Vieth R, Umhau JC, Holick M F, Grant WB, Madronich S, Garland CF and Giovannucci E: Epidemic influenza and vitamin D. Epidemiol Infect. 134:1129–1140. 2006. View Article : Google Scholar : PubMed/NCBI

70 

Mendes MM, Hart KH, Botelho PB and Lanham-New SA: Vitamin D status in the tropics: Is sunlight exposure the main determinant? Nutr Bull. 43:428–434. 2018. View Article : Google Scholar

71 

Huotari A and Herzig KH: Vitamin D and living in northern latitudes-an endemic risk area for vitamin D deficiency. Int J Circumpolar Health. 67:164–178. 2008. View Article : Google Scholar : PubMed/NCBI

72 

Kmiec P, Zmijewski M, Waszak P, Sworczak K and Lizakowska-Kmiec M: Vitamin D deficiency during winter months among an adult, predominantly urban, population in Northern Poland. Endokrynol Pol. 65:105–113. 2014.PubMed/NCBI

73 

Kmiec P, Zmijewski M, Lizakowska-Kmiec M and Sworczak K: Widespread vitamin D deficiency among adults from northern Poland (54°N) after months of low and high natural UVB radiation. Endokrynol Pol. 66:30–38. 2015.

74 

Kroll MH, Bi C, Garber CC, Kaufman HW, Liu D, Caston-Balderrama A, Zhang K, Clarke N, Xie M, Reitz RE, et al: Temporal relationship between vitamin D status and parathyroid hormone in the United States. PLoS One. 10:e01181082015. View Article : Google Scholar : PubMed/NCBI

75 

Greene-Finestone LS, Berger C, de Groh M, Hanley DA, Hidiroglou N, Sarafin K, Poliquin S, Krieger J, Richards JB and Goltzman D; CaMos Research Group: 25-Hydroxyvitamin D in canadian adults: Biological, environmental, and behavioral correlates. Osteoporos Int. 22:1389–1399. 2011. View Article : Google Scholar

76 

Lowen AC, Mubareka S, Steel J and Palese P: Influenza virus transmission is dependent on relative humidity and temperature. PLoS Pathog. 3:1470–1476. 2007. View Article : Google Scholar : PubMed/NCBI

77 

Lowen Ac and Steel J: Roles of humidity and temperature in shaping influenza seasonality. J Virol. 88:7692–7695. 2014. View Article : Google Scholar : PubMed/NCBI

78 

Pham H, Rahman A, Majidi A, Waterhouse M and Neale RE: Acute respiratory tract infection and 25-hydroxyvitamin D concentration: A systematic review and meta-analysis. Int J Environ Res Public Health. 16:30202019. View Article : Google Scholar :

79 

Ilie PC, Stefanescu S and Smith L: The role of vitamin D in the prevention of coronavirus disease 2019 infection and mortality. Aging clin Exp Res. 32:1195–1198. 2020. View Article : Google Scholar : PubMed/NCBI

80 

Hastie CE, Mackay DF, Ho F, Celis-Morales CA, Katikireddi SV, Niedzwiedz CL, Jani BD, Welsh P, Mair FS, Gray SR, et al: Vitamin D concentrations and COVID-19 infection in UK Biobank. Diabetes Metab Syndr. 14:561–565. 2020. View Article : Google Scholar : PubMed/NCBI

81 

D'Avolio A, Avataneo V, Manca A, Cusato J, De Nicolo A, Lucchini R, Keller F and Cantù M: 25-Hydroxyvitamin D concentrations are lower in patients with positive PcR for SARS-coV-2. Nutrients. 12:13592020. View Article : Google Scholar :

82 

Meltzer DO, Best TJ, Zhang H, Vokes T, Arora V and Solway J: Association of vitamin D deficiency and treatment with cOVID-19 incidence. MedRxiv. 2020.05.08.20095893. 2020.

83 

Whittemore PB: COVID-19 fatalities, latitude, sunlight, and vitamin D. Am J Infect control. 48:1042–1044. 2020. View Article : Google Scholar : PubMed/NCBI

84 

Panagiotou G, Tee SA, Ihsan Y, Athar W, Marchitelli G, Kelly D, Boot CS, Stock N, Macfarlane J, Martineau AR, et al: Low serum 25-hydroxyvitamin D (25[OH]D) levels in patients hospitalized with cOVID-19 are associated with greater disease severity. Clin Endocrinol (Oxf). 93:508–511. 2020. View Article : Google Scholar

85 

Merzon E, Tworowski D, Gorohovski A, Vinker S, Golan Cohen A, Green I and Frenkel Morgenstern M: Low plasma 25(OH) vitamin D level is associated with increased risk of COVID-19 infection: An Israeli population-based study. FEBS J. 287:3693–3702. 2020. View Article : Google Scholar : PubMed/NCBI

86 

Batur LK and Hekim N: The role of DBP gene polymorphisms in the prevalence of new coronavirus disease 2019 infection and mortality rate. J Med Virol. Aug 8–2020.Epub ahead of print.

87 

Carpagnano GE, Di Lecce V, Quaranta VN, Zito A, Buonamico E, Capozza E, Palumbo A, Di Gioia G, Valerio VN and Resta O: Vitamin D deficiency as a predictor of poor prognosis in patients with acute respiratory failure due to COVID-19. J Endocrinol Invest. Aug 9–2020.Epub ahead of print. View Article : Google Scholar : PubMed/NCBI

88 

Abrishami A, Dalili N, Mohammadi Torbati P, Asgari R, Arab-Ahmadi M, Behnam B and Sanei-Taheri M: Possible association of vitamin D status with lung involvement and outcome in patients with COVID-19: A retrospective study. Eur J Nutr. Oct 30–2020.Epub ahead of print. View Article : Google Scholar : PubMed/NCBI

89 

De Smet D, De Smet K, Herroelen P, Gryspeerdt S and Martens GA: Serum 25(OH)D level on hospital admission associated with COVID-19 stage and mortality. Am J Clin Pathol. Nov 25–2020.Epub ahead of print. PubMed/NCBI

90 

Ling SF, Broad E, Murphy R, Pappachan JM, Pardesi-Newton S, Kong MF and Jude EB: High-dose cholecalciferol booster therapy is associated with a reduced risk of mortality in patients with COVID-19: A cross-sectional multi-centre observational study. Nutrients. 12:37992020. View Article : Google Scholar :

91 

Faniyi AA, Lugg ST, Faustini SE, Webster C, Duffy JE, Hewison M, Shields A, Nightingale P, Richter AG and Thickett DR: Vitamin D status and seroconversion for COVID-19 in UK healthcare workers. Eur Respir J. Dec 10–2020.Epub ahead of print. View Article : Google Scholar : PubMed/NCBI

92 

Ye K, Tang F, Liao X, Shaw B A, Deng M, Huang G, Qin Z, Peng X, Xiao H, Chen C, et al: Does serum vitamin D level affect COVID-19 infection and its severity?-A case-control study. J Am Coll Nutr. Oct 13–2020.Epub ahead of print. View Article : Google Scholar : PubMed/NCBI

93 

Jain A, Chaurasia R, Sengar NS, Singh M, Mahor S and Narain S: Analysis of vitamin D level among asymptomatic and critically ill COVID-19 patients and its correlation with inflammatory markers. Sci Rep. 10:201912020. View Article : Google Scholar : PubMed/NCBI

94 

Cereda E, Bogliolo L, Klersy C, Lobascio F, Masi S, Crotti S, De Stefano L, Bruno R, Corsico AG, Di Sabatino A, et al: Vitamin D 25OH deficiency in COVID-19 patients admitted to a tertiary referral hospital. Clin Nutr. Nov 2–2020.Epub ahead of print. View Article : Google Scholar : PubMed/NCBI

95 

Annweiler C, Hanotte B, Grandin de l'Eprevier C, Sabatier JM, Lafaie L and Célarier T: Vitamin D and survival in COVID-19 patients: A quasi-experimental study. J Steroid Biochem Mol Biol. 204:1057712020. View Article : Google Scholar : PubMed/NCBI

96 

Annweiler G, Corvaisier M, Gautier J, Dubée V, Legrand E, Sacco G and Annweiler C: Vitamin D supplementation associated to better survival in hospitalized frail elderly COVID-19 patients: The GERIA-COVID Quasi-experimental study. Nutrients. 12:33772020. View Article : Google Scholar :

97 

Entrenas Castillo M, Entrenas Costa LM, Vaquero Barrios JM, Alcala Diaz JF, Lopez Miranda J, Bouillon R and Quesada Gomez JM: 'Effect of calcifediol treatment and best available therapy versus best available therapy on intensive care unit admission and mortality among patients hospitalized for COVID-19: A pilot randomized clinical study'. J Steroid Biochem Mol Biol. 203:1057512020. View Article : Google Scholar

98 

Rastogi A, Bhansali A, Khare N, Suri V, Yaddanapudi N, Sachdeva N, Puri GD and Malhotra P: Short term, high-dose vitamin D supplementation for COVID-19 disease: A randomised, placebo-controlled, study (SHADE study). Postgrad Med J. Nov 12–2020.Epub ahead of print. View Article : Google Scholar : PubMed/NCBI

99 

Pereira M, Dantas Damascena A, Galvâo Azevedo LM, de Almeida Oliveira T and da Mota Santana J: Vitamin D deficiency aggravates COVID-19: Systematic review and meta-analysis. Crit Rev Food Sci Nutr. Nov 4–2020.Epub ahead of print. View Article : Google Scholar

100 

Liu N, Sun J, Wang X, Zhang T, Zhao M and Li H: Low vitamin D status is associated with coronavirus disease 2019 outcomes: A systematic review and meta-analysis. Int J Infect Dis. 104:58–64. 2021. View Article : Google Scholar : PubMed/NCBI

101 

Shoenfeld Y, Giacomelli R, Azrielant S, Berardicurti O, Reynolds JA and Bruce IN: Vitamin D and systemic lupus erythe-matosus-the hype and the hope. Autoimmun Rev. 17:19–23. 2018. View Article : Google Scholar

102 

Cantorna MT, Snyder L, Lin YD and Yang L: Vitamin D and 1,25(OH)2D regulation of T cells. Nutrients. 7:3011–3021. 2015. View Article : Google Scholar : PubMed/NCBI

103 

Zhang YG, Wu S and Sun J: Vitamin D, vitamin D receptor, and tissue barriers. Tissue Barriers. 1:e231182013. View Article : Google Scholar : PubMed/NCBI

104 

Ware LB and Matthay MA: Alveolar fluid clearance is impaired in the majority of patients with acute lung injury and the acute respiratory distress syndrome. Am J Respir Git care Med. 163:1376–1383. 2001. View Article : Google Scholar

105 

Matthay MA, Zemans RL, Zimmerman GA, Arabi YM, Beitler JR, Mercat A, Herridge M, Randolph AG and Calfee Cs: Acute respiratory distress syndrome. Nat Rev Dis Primers. 5:182019. View Article : Google Scholar : PubMed/NCBI

106 

Campbell HK, Maiers JL and DeMali KA: Interplay between tight junctions & adherens junctions. Exp cell Res. 358:39–44. 2017. View Article : Google Scholar : PubMed/NCBI

107 

Chen H, Lu R, Zhang YG and Sun J: Vitamin D receptor deletion leads to the destruction of tight and adherens junctions in lungs. Tissue Barriers. 6:1–13. 2018. View Article : Google Scholar : PubMed/NCBI

108 

Shi YY, Liu TJ, Fu JH, Xu W, Wu LL, Hou AN and Xue XD: Vitamin D/VDR signaling attenuates lipopolysaccharide-induced acute lung injury by maintaining the integrity of the pulmonary epithelial barrier. Mol Med Rep. 13:1186–1194. 2016. View Article : Google Scholar :

109 

Sassi F, Tamone C and D'Amelio P: Vitamin D: Nutrient, hormone, and immunomodulator. Nutrients. 10:16562018. View Article : Google Scholar :

110 

Hewison M: Antibacterial effects of vitamin D. Nat Rev Endocrinol. 7:337–345. 2011. View Article : Google Scholar : PubMed/NCBI

111 

Wei R and Christakos S: Mechanisms underlying the regulation of innate and adaptive immunity by vitamin D. Nutrients. 7:8251–8260. 2015. View Article : Google Scholar : PubMed/NCBI

112 

Chung C, Silwal P, Kim I, Modlin RL and Jo EK: Vitamin D-cathelicidin axis: At the crossroads between protective immunity and pathological inflammation during infection. Immune Netw. 20:e122020. View Article : Google Scholar : PubMed/NCBI

113 

Svensson D, Nebel D, Voss U, Ekblad E and Nilsson BO: Vitamin D-induced up-regulation of human keratinocyte cathelicidin anti-microbial peptide expression involves retinoid X receptor a. cell Tissue Res. 366:353–362. 2016. View Article : Google Scholar : PubMed/NCBI

114 

Schrumpf JA, van Sterkenburg MA, Verhoosel RM, Zuyderduyn S and Hiemstra PS: Interleukin 13 exposure enhances vitamin D-mediated expression of the human cathelicidin antimicrobial peptide 18/LL-37 in bronchial epithelial cells. Infect Immun. 80:4485–4494. 2012. View Article : Google Scholar : PubMed/NCBI

115 

Kim EW, Teles RMB, Haile S, Liu PT and Modlin RL: Vitamin D status contributes to the antimicrobial activity of macrophages against mycobacterium leprae. PLoS Negl Trop Dis. 12:e00066082018. View Article : Google Scholar : PubMed/NCBI

116 

Fabri M, Stenger S, Shin DM, Yuk JM, Liu PT, Realegeno S, Lee HM, Krutzik SR, Schenk M, Sieling PA, et al: Vitamin D is required for IFN-gamma-mediated antimicrobial activity of human macrophages. Sci Transl Med. 3:104ra1022011. View Article : Google Scholar : PubMed/NCBI

117 

Martineau AR, Wilkinson KA, Newton SM, Floto RA, Norman AW, Skolimowska K, Davidson RN, Sørensen OE, Kampmann B, Griffiths CJ and Wilkinson RJ: IFN-gamma- and TNF-independent vitamin D-inducible human suppression of mycobacteria: The role of cathelicidin LL-37. J Immunol. 178:7190–7198. 2007. View Article : Google Scholar : PubMed/NCBI

118 

Piemonti L, Monti P, Sironi M, Fraticelli P, Leone BE, Dal cin E, Allavena P and Di carlo V: Vitamin D3 affects differentiation, maturation, and function of human monocyte-derived dendritic cells. J Immunol. 164:4443–4451. 2000. View Article : Google Scholar : PubMed/NCBI

119 

Széles L, Keresztes G, Töröcsik D, Balajthy Z, Krenacs L, Poliska S, Steinmeyer A, Zuegel U, Pruenster M, Rot A and Nagy L: 1,25-dihydroxyvitamin D3 is an autonomous regulator of the transcriptional changes leading to a tolerogenic dendritic cell phenotype. J Immunol. 182:2074–2083. 2009. View Article : Google Scholar : PubMed/NCBI

120 

Aranow C: Vitamin D and the immune system. J Investig Med. 59:881–886. 2011. View Article : Google Scholar : PubMed/NCBI

121 

Prietl B, Treiber G, Pieber TR and Amrein K: Vitamin D and immune function. Nutrients. 5:2502–2521. 2013. View Article : Google Scholar : PubMed/NCBI

122 

Alroy I, Towers TL and Freedman LP: Transcriptional repression of the interleukin-2 gene by vitamin D3: Direct inhibition of NFATp/AP-1 complex formation by a nuclear hormone receptor. Mol Cell Biol. 15:5789–5799. 1995. View Article : Google Scholar : PubMed/NCBI

123 

Cippitelli M and Santoni A: Vitamin D3: A transcriptional modulator of the interferon-gamma gene. Eur J Immunol. 28:3017–3030. 1998. View Article : Google Scholar : PubMed/NCBI

124 

Palmer MT, Lee YK, Maynard CL, Oliver JR, Bikle DD, Jetten AM and Weaver CT: Lineage-specific effects of 1.25-dihydroxyvitamin D(3) on the development of effector CD4 T cells. J Biol Chem. 286:997–1004. 2011. View Article : Google Scholar

125 

Dankers W, Colin EM, van Hamburg JP and Lubberts E: Vitamin D in autoimmunity: molecular mechanisms and therapeutic potential. Front Immunol. 7:6972017. View Article : Google Scholar : PubMed/NCBI

126 

Tang J, Zhou R, Luger D, Zhu W, Silver PB, Grajewski RS, Su SB, Chan CC, Adorini L and Caspi RR: Calcitriol suppresses antiretinal autoimmunity through inhibitory effects on the Th17 effector response. J Immunol. 182:4624–4632. 2009. View Article : Google Scholar : PubMed/NCBI

127 

Wöbke TK, Sorg BL and Steinhilber D: Vitamin D in inflammatory diseases. Front Physiol. 5:2442014.PubMed/NCBI

128 

Cohen-Lahav M, Shany S, Tobvin D, Chaimovitz C and Douvdevani A: Vitamin D decreases NFkappaB activity by increasing IkappaBalpha levels. Nephrol Dial Transplant. 21:889–897. 2006. View Article : Google Scholar : PubMed/NCBI

129 

Harant H, Wolff B and Lindleyl J: 1Alpha,25-dihydroxyvitaminD3 decreases DNA binding of nuclear factor-kappa B in human fibroblasts. FEBS Lett. 436:329–334. 1998. View Article : Google Scholar : PubMed/NCBI

130 

Sloka S, Silva C, Wang J and Yong VW: Predominance of Th2 polarization by vitamin D through a STAT6-dependent mechanism. J Neuroinflammation. 8:562011. View Article : Google Scholar : PubMed/NCBI

131 

Calton EK, Keane KN, Newsholme P and Soares MJ: The impact of vitamin D levels on inflammatory status: A systematic review of immune cell studies. PLoS One. 10:e01417702015. View Article : Google Scholar : PubMed/NCBI

132 

Ho IC, Tai TS and Pai SY: GATA3 and the T-cell lineage: Essential functions before and after T-helper-2-cell differentiation. Nat Rev Immunol. 9:125–135. 2009. View Article : Google Scholar : PubMed/NCBI

133 

Baeke F, Takiishi T, Korf H, Gysemans C and Mathieu C: Vitamin D: Modulator of the immune system. Curr Opin Pharmacol. 10:482–496. 2010. View Article : Google Scholar : PubMed/NCBI

134 

Joshi S, Pantalena LC, Liu XK, Gaffen SL, Liu H, Rohowsky-Kochan C, Ichiyama K, Yoshimura A, Steinman L, Christakos S and Youssef S: 1,25-dihydroxyvitamin D(3) ameliorates Th17 autoimmunity via transcriptional modulation of interleukin-17A. Mol Cell Biol. 31:3653–3669. 2011. View Article : Google Scholar : PubMed/NCBI

135 

Jeffery LE, Burke F, Mura M, Zheng Y, Qureshi OS, Hewison M, Walker LS, Lammas DA, Raza K and Sansom DM: 1.25-Dihydroxyvitamin D3 and IL-2 combine to inhibit T cell production of inflammatory cytokines and promote development of regulatory T cells expressing CTLA-4 and FoxP3. J Immunol. 183:5458–5467. 2009. View Article : Google Scholar : PubMed/NCBI

136 

Nanduri R, Mahajan S, Bhagyaraj E, Sethi K, Kalra R, Chandra V and Gupta P: The active form of vitamin D transcriptionally represses Smad7 signaling and activates extracellular signal-regulated kinase (ERK) to inhibit the differentiation of a inflammatory T helper cell subset and suppress experimental autoimmune encephalomyelitis. J Biol Chem. 290:12222–12236. 2015. View Article : Google Scholar : PubMed/NCBI

137 

Li YC: Vitamin D regulation of the renin-angiotensin system. J Cell Biochem. 88:327–331. 2003. View Article : Google Scholar : PubMed/NCBI

138 

Fountain JH and Lappin SL: Physiology, Renin Angiotensin System. StatPearls Publishing; Treasure Island, FL: 2020

139 

Mahmudpour M, Roozbeh J, Keshavarz M, Farrokhi S and Nabipour I: COVID-19 cytokine storm: The anger of inflammation. Cytokine. 133:1551512020. View Article : Google Scholar : PubMed/NCBI

140 

Aygun H: Vitamin D can prevent COVID-19 infection-induced multiple organ damage. Naunyn Schmiedebergs Arch Pharmacol. 393:1157–1160. 2020. View Article : Google Scholar : PubMed/NCBI

141 

Ajabshir S, Asif A and Nayer A: The effects of vitamin D on the renin-angiotensin system. J Nephropathol. 3:41–43. 2014.PubMed/NCBI

142 

Yuan W, Pan W, Kong J, Zheng W, Szeto FL, Wong KE, Cohen R, Klopot A, Zhang Z and Li YC: 1,25-dihydroxyvitamin D3 suppresses renin gene transcription by blocking the activity of the cyclic AMP response element in the renin gene promoter. J Biol Chem. 282:29821–29830. 2007. View Article : Google Scholar : PubMed/NCBI

143 

Melamed ML, Michos ED, Post W and Astor B: 25-hydroxyvitamin D levels and the risk of mortality in the general population. Arch Intern Med. 168:1629–1637. 2008. View Article : Google Scholar : PubMed/NCBI

144 

Cashman KD, van den Heuvel EG, Schoemaker RJ, Preveraud DP, Macdonald HM and Arcot J: 25-Hydroxyvitamin D as a biomarker of vitamin D status and its modeling to inform strategies for prevention of vitamin D deficiency within the population. Adv Nutr. 8:947–957. 2017. View Article : Google Scholar : PubMed/NCBI

145 

Norval M and Wulf HC: Does chronic sunscreen use reduce vitamin D production to insufficient levels? Br J Dermatol. 161:732–736. 2009. View Article : Google Scholar : PubMed/NCBI

146 

Neale RE, Khan SR, Lucas RM, Waterhouse M, Whiteman DC and Olsen CM: The effect of sunscreen on vitamin D: A review. Br J Dermatol. 181:907–915. 2019. View Article : Google Scholar : PubMed/NCBI

147 

Brenner M and Hearing VJ: The protective role of melanin against UV damage in human skin. Photochem Photobiol. 84:539–549. 2008. View Article : Google Scholar : PubMed/NCBI

148 

Vranic L, Mikolasevic I and Milic S: Vitamin D deficiency: Consequence or cause of obesity? Medicina (Kaunas). 55:5412019. View Article : Google Scholar

149 

Iruzubieta P, Teran A, Crespo J and Fabrega E: Vitamin D deficiency in chronic liver disease. World J Hepatol. 6:901–915. 2014. View Article : Google Scholar : PubMed/NCBI

150 

Goldstein DA, Haldimann B, Sherman D, Norman AW and Massry SG: Vitamin D metabolites and calcium metabolism in patients with nephrotic syndrome and normal renal function. J clin Endocrinol Metab. 52:116–121. 1981. View Article : Google Scholar : PubMed/NCBI

151 

Banerjee S, Basu S, Akhtar S, Sinha R, Sen A and Sengupta J: Free vitamin D levels in steroid-sensitive nephrotic syndrome and healthy controls. Pediatr Nephrol. 35:447–454. 2020. View Article : Google Scholar

152 

Skversky AL, Kumar J, Abramowitz MK, Kaskel FJ and Melamed ML: Association of glucocorticoid use and low 25-hydroxyvitamin D levels: Results from the national health and nutrition examination survey (NHANEs): 2001-2006. J Clin Endocrinol Metab. 96:3838–3845. 2011. View Article : Google Scholar : PubMed/NCBI

153 

Fernandez H, Mohammed HT and Patel T: Vitamin D supplementation for bone health in adults with epilepsy: A systematic review. Epilepsia. 59:885–896. 2018. View Article : Google Scholar : PubMed/NCBI

154 

Zhou C, Assem M, Tay JC, Watkins PB, Blumberg B, Schuetz EG and Thummel KE: steroid and xenobiotic receptor and vitamin D receptor crosstalk mediates cYP24 expression and drug-induced osteomalacia. J Clin Invest. 116:1703–1712. 2006. View Article : Google Scholar : PubMed/NCBI

155 

Al-Badr W and Martin KJ: Vitamin D and Kidney Disease. Clin J Am Soc Nephrol. 3:1555–1560. 2008. View Article : Google Scholar : PubMed/NCBI

156 

Chung S, Kim M, Koh ES, Hwang HS, Chang YK, Park CW, Kim SY, Chang YS and Hong YA: serum 1,25-dihydroxyvitamin D better reflects renal parameters than 25-hydoxyvitamin D in patients with glomerular diseases. Int J Med Sci. 14:1080–1087. 2017. View Article : Google Scholar : PubMed/NCBI

157 

Dastani Z, Li R and Richards B: Genetic regulation of vitamin D levels. Calcif Tissue Int. 92:106–117. 2013. View Article : Google Scholar

158 

Wang TJ, Zhang F, Richards JB, Kestenbaum B, van Meurs JB, Berry D, Kiel DP, streeten EA, Ohlsson C, Koller DL, et al: Common genetic determinants of vitamin D insufficiency: A genome-wide association study. Lancet. 376:180–188. 2010. View Article : Google Scholar : PubMed/NCBI

159 

Alshahrani FM, Almalki MH, Aljohani N, Alzahrani A, Alsaleh Y and Holick MF: Vitamin D: Light side and best time of sunshine in Riyadh, audi Arabia. Dermatoendocrinol. 5:177–180. 2013. View Article : Google Scholar

160 

Gallagher JC: Vitamin D and aging. Endocrinol Metab Clin North Am. 42:319–332. 2013. View Article : Google Scholar : PubMed/NCBI

161 

Margulies SL, Kurian D, Elliott MS and Han Z: Vitamin D deficiency in patients with intestinal malabsorption syndromes-think in and outside the gut. J Dig Dis. 16:617–633. 2015. View Article : Google Scholar : PubMed/NCBI

162 

Robien K, Oppeneer SJ, Kelly JA and Hamilton-Reeves JM: Drug-vitamin D interactions: A systematic review of the literature. Nutr Clin Pract. 28:194–208. 2013. View Article : Google Scholar : PubMed/NCBI

163 

Cembranel F, D'Orsi E, Jakovljevic Pudla Wagner K, Weber Corseuil Giehl M, Moreno YMF and Gonzalez-Chica DA: Obesity and 25(OH)D serum concentration are more important than vitamin D intake for changes in nutritional status indicators: A population-based longitudinal study in a state capital city in Southern Brazil. Nutrients. 11:23662019. View Article : Google Scholar :

164 

Martrnez-Zavala N, Löpez-Sanchez GN, Vergara-Lopez A, Chavez-Tapia NC, Uribe M and Nuno-Lambarri N: Vitamin D deficiency in Mexicans have a high prevalence: A cross-sectional analysis of the patients from the centro Médico Nacional 20 de Noviembre. Arch Osteoporos. 15:882020. View Article : Google Scholar

165 

Tomaino K, Romero KM, Robinson CL, Baumann LM, Hansel NN, Pollard SL, Gilman RH, Mougey E, Lima JJ and Checkley W; PURA study investigators: Association between serum 25-hydroxy vitamin D levels and blood pressure among adolescents in two resource-limited settings in Peru. Am J Hypertens. 28:1017–1023. 2015. View Article : Google Scholar : PubMed/NCBI

166 

Solis-Urra P, Cristi-Montero C, Romero-Parra J, Zavala-Crichton JP, Saez-Lara MJ and Plaza-Diaz J: Passive commuting and higher sedentary time is associated with vitamin D deficiency in adult and older women: Results from Chilean national health survey 2016-2017. Nutrients. 11:3002019. View Article : Google Scholar

167 

Hernando VU, Andry MM, Maria Virginia PF and Valentina A: Vitamin D nutritional status in the adult population in Colombia-an analytical cross-sectional study. Heliyon. 6:e034792020. View Article : Google Scholar

168 

Ross AC, Manson JE, Abrams SA, Aloia JF, Brannon PM, Clinton SK, Durazo-Arvizu RA, Gallagher JC, Gallo RL, Jones G, et al: The 2011 report on dietary reference intakes for calcium and vitamin D from the institute of medicine What clinicians need to know. J Clin Endocrinol Metab. 96:53–58. 2011. View Article : Google Scholar

169 

Holick MF, Binkley NC, Bischoff-Ferrari HA, Gordon CM, Hanley DA, Heaney RP, Murad MH, Weaver CM and Endocrine Society: Evaluation, treatment, and prevention of vitamin D deficiency: An endocrine society clinical practice guideline. J Clin Endocrinol Metab. 96:1911–1930. 2011. View Article : Google Scholar : PubMed/NCBI

170 

Palacios C and Gonzalez L: Is vitamin D deficiency a major global public health problem? J Steroid Biochem Mol Biol. 144:138–145. 2014. View Article : Google Scholar

171 

Dobson R, Cock HR, Brex P and Giovannoni G: Vitamin D supplementation. Pract Neurol. 18:35–42. 2018. View Article : Google Scholar

172 

EFSA Panel on Dietetic Products Nutrition and Allergies (NDA): Scientific opinion on the tolerable upper intake level of vitamin D. EFSA J. 10:28132012.

173 

Scientific Advisory Committee on Nutrition: Vitamin D and Health. 2016.

174 

Ebadi M and Montano-Loza AJ: Perspective: Improving vitamin D status in the management of COVID-19. Eur J Clin Nutr. 74:856–859. 2020. View Article : Google Scholar : PubMed/NCBI

175 

Maeda SS, Borba VZ, Camargo MB, Silva DM, Borges JL, Bandeira F and Lazaretti-Castro M: Recomendaçôes da Sociedade Brasileira de Endocrinologia e Metabologia (SBEM) para o diagnostico e tratamento da hipovitaminose D. Arq Bras Endocrinol Metabol. 58:411–433. 2014. View Article : Google Scholar : PubMed/NCBI

176 

Ministerio de Salud del Gobierno de Chile: Estudio para revision y actualization de las guias alimentarias para la poblacion chilena. 2013.

177 

Vasquez-Awad D, Cano-Gutiérrez CA, Gomez-Ortiz A, Gonzalez MA, Guzman-Moreno R, Martinez-Reyes JI, Rosero-Olarte O, Rueda-Beltz C and Acosta-Reyes JL: Vitamina D. Consenso colombiano de expertos. Medicina. 39:140–157. 2017.

178 

Lopez-Gonzalez D, Méndez-Sanchez L, Guagnelli MA and Clark P: Deficiencia de vitamina D en la edad pediatrica. una oportunidad de prevencion. Bol Med Hosp Infant Mex. 72:225–234. 2015.

179 

Pludowski P, Holick MF, Grant WB, Konstantynowicz J, Mascarenhas MR, Haq A, Povoroznyuk V, Balatska N, Barbosa AP, Karonova T, et al: Vitamin D supplementation guidelines. J Steroid Biochem Mol Biol. 175:125–135. 2018. View Article : Google Scholar

180 

Grant WB, Lahore H, McDonnell SL, Baggerly CA, French CB, Aliano JL and Bhattoa HP: Evidence that vitamin D supplementation could reduce risk of influenza and COVID-19 infections and deaths. Nutrients. 12:9882020. View Article : Google Scholar :

181 

Goddek S: Vitamin D3 and K2 and their potential contribution to reducing the COVID-19 mortality rate. Int J Infect Dis. 99:286–290. 2020. View Article : Google Scholar : PubMed/NCBI

Related Articles

Journal Cover

April-2021
Volume 47 Issue 4

Print ISSN: 1107-3756
Online ISSN:1791-244X

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Turrubiates‑Hernández FJ, Sánchez‑Zuno GA, González‑Estevez G, Hernández‑Bello J, Macedo‑Ojeda G and Muñoz‑Valle JF: Potential immunomodulatory effects of vitamin D in the prevention of severe coronavirus disease 2019: An ally for Latin America (Review). Int J Mol Med 47: 32, 2021.
APA
Turrubiates‑Hernández, F.J., Sánchez‑Zuno, G.A., González‑Estevez, G., Hernández‑Bello, J., Macedo‑Ojeda, G., & Muñoz‑Valle, J.F. (2021). Potential immunomodulatory effects of vitamin D in the prevention of severe coronavirus disease 2019: An ally for Latin America (Review). International Journal of Molecular Medicine, 47, 32. https://doi.org/10.3892/ijmm.2021.4865
MLA
Turrubiates‑Hernández, F. J., Sánchez‑Zuno, G. A., González‑Estevez, G., Hernández‑Bello, J., Macedo‑Ojeda, G., Muñoz‑Valle, J. F."Potential immunomodulatory effects of vitamin D in the prevention of severe coronavirus disease 2019: An ally for Latin America (Review)". International Journal of Molecular Medicine 47.4 (2021): 32.
Chicago
Turrubiates‑Hernández, F. J., Sánchez‑Zuno, G. A., González‑Estevez, G., Hernández‑Bello, J., Macedo‑Ojeda, G., Muñoz‑Valle, J. F."Potential immunomodulatory effects of vitamin D in the prevention of severe coronavirus disease 2019: An ally for Latin America (Review)". International Journal of Molecular Medicine 47, no. 4 (2021): 32. https://doi.org/10.3892/ijmm.2021.4865