The IL-2 family of cytokines has been extensively studied in the field of cancer immunotherapy (9). IL-2 is produced by antigen-activated CD4⁺ T cells, CD8⁺ T cells, NK cells and NKT cells (9). IL-2 serves roles in the regulation, proliferation and activation of Tregs, CD4⁺ and CD8⁺ T cells, B cells, mature dendritic cells (DCs) and endothelial cells (9). The main challenge in using IL-2 in immunotherapy lies in the differential expression of the IL-2 α receptor (IL-2Rα) on various types of cells, as IL-2 affects peripheral Tregs (CD25⁺, CD4⁺ and Foxp3⁺) more efficiently than effector T cells (CD8⁺ and NK cells) (10). IL-2Rα and IL-2Rβγ are constitutively expressed on Tregs at high levels (10). This allows Tregs to respond to low doses of IL-2 in order to prevent autoimmune pathologies, and thus suppress the immune response (9). By contrast, CD4⁺, CD8⁺ and NK cells respond only to high doses of IL-2 due to the transient expression of the receptor, which is regulated by multiple transcription factors including nuclear factor of activated T cells, NF-κB and activator protein 1 (10). The key for using cytokines in cancer treatment lies in increasing the antitumor activity of CD8⁺ T cells and NK cells, while counteracting the immunosuppressive activity of regulatory T cells that can hinder the response of the effector cells (10).

High doses of IL-2 have been demonstrated to increase the activity of low-IL-2 affinity cells (NK and CD8⁺) and to initiate an antitumor response (11). However, this response is largely suppressed and counteracted by the increased activity of Tregs; a response rate of only 12.5% was observed in patients with metastatic cancer who received successive high doses of IL-2 (11). On the other hand, low doses of IL-2 activate the high-affinity receptors present only in Tregs, thus preventing the activation of the antitumor immune response (11). As a result, previous studies have used varying approaches to eliminate the counteraction of Tregs on the activation of effector T cells and NK cells. One of the main approaches involves using the ALKS 4230 protein, a fusion protein of the circularly permutated IL-2 and the extracellular domain of IL-2Rα (12). This method targets IL-2 to the intermediate-affinity receptors expressed by NK and CD8⁺ cells and not the high-affinity receptors expressed by immunosuppressive cells (12). A previous study has demonstrated that ALKS 4230 lowers the frequency of toxicity incidents occurring in patients undergoing a high-IL-2 dosage regimen and improves the antitumor efficacy by counteracting the immunosuppressive pathway (12). ALKS4230 is currently being considered as a potential cancer immunotherapy treatment (12). Other immunotherapy approaches focus on using IL-21 rather than IL-2 (12). IL-21 has been demonstrated to activate NK cells, while poorly activating T cells, including Tregs; IL-21 does not promote the proliferation and activation of CD4⁺, CD25⁺ and Fox3⁺ cells nor the secretion of IL-2 (13). In the absence of IL-2, IL-21 is unable to compensate for IL-2 by maintaining the production and activation of Tregs (13). However, IL-21 is capable of promoting the proliferation of NK and CD2⁺ T cells (13). Thus, IL-21 indirectly counteracts the immunosuppressive effect of Tregs, while maintaining the proliferation of NK and effector T cells (13). IL-21 has been demonstrated to be relatively safe and tolerated, in contrast to IL-2 treatment, which leads to Vascular Leak Syndrome (13).

The serum half-life of IL-2 is only 7 min; thus, for effective treatment, patients would have to receive a high dose of IL-2 every 8 h (14). However, due to the presence of high-affinity IL-2 receptors on endothelial cells, consecutive high doses of IL-2 may lead to toxicity including capillary leak syndrome, which causes a sudden drop in blood pressure that can potentially lead to organ failure and death (14). To solve this issue, a number of studies have examined the impact of the conjugation of IL-2 to PEG polymers on its serum half-life. PEGylated IL-2 (PEG–IL-2) has been demonstrated to have the same activity as IL-2, but with a 200% increase in circulating half-life (14). Addition of Polyethylene glycol to IL-2 increases its retention by protecting it from enzymatic digestion and renal clearance, thus increasing its serum half-life to 1 day (14). In a study where patients treated with two cycles of high dose unconjugated IL-2 were compared with patients receiving a hybrid regimen combining an initial high dose of IL-2 with successive weekly doses of PEG-IL-2, the results revealed that the relative response rate to unconjugated IL-2 was 19%, compared with 17% for the combination of IL-2 and PEG-IL-2 combination (14). Thus, the use of high-dose IL-2 followed by PEG-IL-2 is a well-tolerated regimen that decreases the side effects of constant high IL-2 doses, but has no significant effects on the antitumor activity compared with high IL-2 dosages in patients with renal cell cancer and metastatic melanoma (14).

IL-2 cancer therapy has been studied as a monotherapy and in combination with other therapeutic approaches including chemotherapy, peptide vaccines and other combinations of cytokines (15). IL-2 immunotherapy has been approved by the US FDA for the treatment of solid tumors such as metastatic renal cancer and melanoma. In a study where patients were administered a high dose of IL-2 (600,000-720,000 IU/kg) every 8 h, the overall response rate was 15%, with a complete response rate of 7% (16). Another study used IL-2 in combination with lymphokine activated killer (LAK) cells, and an overall response rate of 25–30% was observed (16). A subsequent study focused on combining ex vivo expanded tumor infiltrating lymphocytes (TILs) with a high-dose IL-2 regimen and lymphodepletion for the treatment of patients with metastatic melanoma (17). In this approach, TILs were rapidly expanded in the presence of anti-CD3, feeder cells and IL-2, and infused into the patients, and an overall response of 50% was reported in patients with metastatic melanoma (17).

The effective use of IL-2 in cancer treatment is hampered by several drawbacks, the main one being its short serum half-life, which is mostly due to rapid metabolism and elimination by the kidneys (18). Thus, IL-2 has to be administered repeatedly (every 8 h) at high doses, which can lead to severe toxicity such as hypotension, cardiac problems and pulmonary edema (18). In addition, Krieg et al (18) have reported that the binding of IL-2 to high-affinity IL-2Ra-expressing endothelial cells causes acute vasodilation effects that, in turn, lead to the development of vascular leak syndrome.

Cytokines are a diverse group of molecules, each of which can be used to target specific cells and activate unique pathways to obtain an overall therapeutic effect. Cytokines can also be combined with other therapeutic agents that work synergistically in order to provide significant advantages over monotherapy (19). Ovarian cancer is a type of cancer in which combination immunotherapy has shown promising results; one of the emerging therapies for ovarian cancer is targeting its arginine auxotrophy by depriving it of arginine, using a recombinant human arginase, inducing autophagy and subsequenT cell death (19). On the other hand, combination immunotherapy has also been effective in the treatment of ovarian cancer. A study by Ingersoll et al has demonstrated that combining cellular therapy using peripheral blood mononuclear cells with IL-2 and IFN cytokines significantly increases the survival of an ovarian cancer xenograft mouse model (20). This is consistent with another study that has reported that such a combination also exhibited increased cytotoxic effects on two ovarian cancer cell lines compared with those of monotherapy (21). Additionally, combining interferon α-2b and interleukin-2 cytokine treatment with adoptive cell transfer and cryosurgery has demonstrated promising results in patients with advanced oral mucosa melanoma (21).

IL-2 has been extensively studied in renal cancer and melanoma; however, other interleukins are also emerging in the field of cancer immunotherapy (16). Interleukins such as IL-15, IL-10 and IL-21 are of major importance in cancer immunotherapeutic studies (7). IL-5 binds to the same receptor as IL-2 and activates STAT5 (7). However, IL-5 initiates a different downstream signaling pathway, which has different effects on CDC8⁺ cell differentiation and memory cell formation (3).

IL-15 is crucial for the proliferation and maintenance of memory T cells as well as for promoting the survival and increasing the cytotoxicity of NK and CD8⁺ T cells (22). IL-15 also induces the release and proliferation of other proinflammatory cytokines such as IFN-γ (22). Notably, IL-15 has no affinity for the IL-2Rα chain (CD25) and thus does not activate Tregs (22). As a result, IL-15 has been extensively studied as an alternative of IL-2 in cancer immunotherapy. For example, in a recent clinical trial, patients with renal cell carcinoma, non-small cell lung cancer (NSCLC) and melanoma received subcutaneous IL-15 injections, and the results demonstrated a dose-dependent increase in the number of active NK cells (23). In addition, a number of patients exhibited marked disease stabilization, especially patients with renal cell carcinoma, who presented with >2 years of increased disease stability (23). However, one study reported that IL-15 has a very short serum half-life of only 2.5 h due to its small size, resulting in rapid elimination from circulation (24). In addition, high doses of IL-15 have deleterious effects on the lymphocytes (22). Thus, trans-presentation has been adopted as a solution for this issue by increasing the specificity of IL-15 and increasing its half-life (25).

IL-15 binds to the high-affinity IL-15 receptor IL-15Rα on the cell surface, which stimulates IL-15 signaling in the neighboring cells (26). This process is of great importance in activating the cytotoxic immune response and has been studied as an approach to stimulate direct cytokine delivery to responsive cells (26).

Several studies have focused on engineering IL-15 variants with a longer half-life (27–29). One of the promising fusion proteins includes the RNase L inhibitor protein, where IL-15 is fused to the binding domain of IL-15Rα, also termed the sushi domain (27). This fusion protein was shown to increase the survival of mice bearing multiple myeloma (29). Another study focused on constructing a triple-fusion protein termed Sushi-IL15-Apo (28). The Sushi-IL15-Apo protein comprises the fusion of human IL-15 to the sushi domain and to apolipoprotein A-I (28). The receptor of the apolipoprotein A-I is expressed at high levels in tumor cells, and thus IL-15 activity can be specifically targeted to tumor cells (28).

Another fusion protein of IL-15 is ALT-803, in which IL-15 is fused to the sushi domain and an IgG1 Fc domain (29). A study in mice has reported that this fusion protein successfully promotes IL-2 activity (29). In a dose-escalation phase I clinical study, patients with hematological cancer received ALT-803 following relapse in response to the allotransplantation of bone marrow (30). Treatment with the fusion protein was well-tolerated in all patients, and the results demonstrated increased numbers of NK and CD8⁺ cells (30). Another study has reported that ALT-803 in combination with intravesical bacillus Calmette-Guérin therapy exhibited sustained and complete responses in nine patients with localized bladder cancer; as a result, this combination treatment was approved by the FDA for non-muscle invasive bladder cancer (31). A study investigated the use in IL-15 in combination therapies and as an adjuvant in T- or NK-cell therapies (31).

Another cytokine from the IL-2 family is IL-21, which exerts poor effects on the activation of Tregs, but is considered a potent driver of NK cell activation and proliferation (7). IL-21 has been studied alone and in combination therapies in cancer trials (7,32). In a study of the combination therapy of IL-21 with rituximab in patients with non-Hodgkin lymphoma, eight out of 19 patients presented with promising clinical responses (32). However, clinical trials with IL-21 are still minimal, and future studies are required that focus on its use in combination therapy.

Anti-inflammatory cytokines such as IL-10 are also a major subject of cancer immunotherapy studies. Although IL-10 inhibits the cytokine release in T and NK cells, a previous study has highlighted that IL-10 inhibits antigen-induced apoptosis of cytotoxic T cells (CD8⁺) in cases of chronic infections and tumors (33). This was demonstrated in a phase I clinical trial of patients treated with PEG-conjugated IL-10; the results were promising, with only 15% of patients presenting with grade 3 immune adverse effects and PEG-IL-10 being well tolerated in the majority of the patients (33). The current focus is on the use of IL-10 in combination therapy with vaccines or other chemotherapeutic agents (34).

A number of other cytokines, including IFN-α and TNF-α, have been extensively studied in cancer immunotherapy. In 1986, IFN-α was approved by the FDA for the treatment of patients with hairy cell leukemia (35). Since then, it has been a candidate for the treatment of solid tumors and other hematological malignancies at high doses (35). A major study has demonstrated that high doses of IFN-α trigger apoptosis and inhibit the proliferation of cancer cells (35).

Similar to other cytokines, extending the serum half-life of IFN-α has also been achieved through PEGylation (36). PEG-IFN-α has been approved as an adjuvant in the treatment of melanoma (36). A previous study focusing on IFN-α in combination therapies has reported that IFN-α increases patient survival rates by enhancing the antitumor responses of cytotoxic chemotherapies (37). However, the issue with IFN-α is that high doses induce autoimmune responses due to its role in potentiating dendritic cells, which induce cross-priming of apoptotic antigens to cytotoxic T cells (38). One method to overcome the cytotoxic activity of IFN-α and only provoke the immune-stimulatory activity involves the fusion of IFN-α to apolipoprotein A-I (39). Apo-IFN-α exhibits an increased half-life, enhanced immunostimulatory activity and tumor targeting, as well as decreased cytotoxicity compared with those of IFN-α (39).

Other approaches to overcome the cytotoxicity of IFN-α focus on fusing a mutated IFN-α with reduced affinity for its receptor to a cell-specific targeting domain C-type lectin domain-containing 9A, which is a molecule expressed on cross-priming specialized dendritic cells (40). The mutated cytokines termed activity-on-target cytokines, or AcTakines, exhibit strong antitumor activity in lymphoma, breast carcinoma and melanoma in humanized mice with no side effects (40).

Another cytokine that may be used as a potential cancer therapeutic is the TNF-α. This pro-inflammatory cytokine is secreted mainly by antigen-presenting cells such as monocytes, macrophages and DCs, as well as by other cell types such as endothelial cells, fibroblasts and adipocytes under acute inflammation and stress conditions (41). TNF-α was the first cytokine studied for cancer immunotherapy (41). Numerous studies have focused on the tumor cell apoptosis and antitumor activity of TNF-α in various malignancies, such as AIDS-associated Kaposi's sarcoma (41–44). Phase I clinical trials of TNF-α have revealed dose-limiting toxicities such as nausea, vomiting, anorexia, hypotension and thrombocytopenia, with little to no tumor response (42). Chronic TNF-α exposure also induced the cell death of T lymphocytes and, as a result, promoted tumor growth (43).

Considering the range of toxicities observed in animal studies, the antitumor efficacy of TNF-α in humans was not evident; however, a number of studies described the localized administration of TNF-α in patients as an approach to avoid the toxicities associated with its systemic use (44–46). In a study on localized intratumoral administration of TNF-α to patients with Kaposi's sarcoma, the results demonstrated a reduction in the cancer lesions in 15 out of 16 patients (44).

A clinically successful approach of TNF-α therapy is its use in combination with the alkylating agent melphalan in isolated limb perfusion protocols (45). This combination therapy approach has also been adopted for patients with soft tissue sarcomas and melanomas and has exhibited an 80% complete response rate (45). The high response rates were associated with increased endothelium permeability, facilitating the diffusion of chemotherapy into the tumor and the direct killing of the tumor endothelium (45). In addition, tumor vascular collapse and hemorrhagic necrosis were observed upon TNF-α and melphalan administration (46). TNF-α-ILP therapy was approved for high-grade soft tissue carcinoma treatment in Europe in 1998 (47).

Cytokines are potent yet complex immune mediators that still require extensive research. Future research should focus on two main approaches in cytokine therapies: Limiting the effects of cytokines at the site of tumor to avoid systemic inflammatory side effects and studying the efficacy of these treatments in combination therapies.

Numerous studies have tested the efficacy and biological effects of CTLA-4 and PD-1 blockage through either monotherapy or combined therapy. For instance, to test for the efficiency of ICIs in advanced melanoma, Wolchok et al (50) randomly treated previously untreated patients with either the anti-CTLA-4 human monoclonal antibody ipilimumab monotherapy, the anti-PD-1 antibody Nivolumab monotherapy or a combination of ipilimumab and Nivolumab. Assessment of the results was based on three variables: i) Overall survival (OS), the time from randomization of treatments until death; ii) objective response rate (ORR), the ratio of patients that exhibited partial or complete response to a specific treatment; and iii) the rate of progression-free survival (PFS), the time elapsed between randomization and the first documented disease or death (50). The results demonstrated that patients who underwent combined treatment exhibited the highest ORR (58%), a higher rate of PFS (11.5 months) and the highest rate of OS among the three groups throughout a 3-year analysis period (50). This was compared with a 44 and 19% ORR, 6.9 and 2.9 months of PFS, and 52 and 34% OS rate in patients that underwent Nivolumab and ipilimumab monotherapy, respectively (50). Therefore, for previously untreated patients with advanced melanoma, more promising results were observed using the combination therapy of Nivolumab and Ipilimumab compared with either treatment alone (50).

Although NSCLC is a poorly immunogenic malignancy, ICIs may be encouraging therapeutic agents for this type of tumor, as they exhibit antitumor activity (50). As previously reported for patients with advanced melanoma, monotherapy of the anti-CTLA-1 antibody ipilimumab leads to an improvement in the OS rate (50). However, this is not the case for patients with NSCLC, unless ipilimumab is combined with other immunotherapies, such as PD-1 inhibitors (48). When patients with NSCLC were treated with both ipilimumab and Nivolumab using the same doses used in previous studies for the treatment of melanoma, the ORR was 16%, but was accompanied by a high rate of grade 3/4 treatment-related AEs and treatment-related discontinuations (49 and 35%, respectively) (48). However, when the doses were adjusted, increased tolerability and positive antitumor activities were observed in the patients, with the ORR of 39–47% and a decrease in the rate of treatment-related discontinuation to 13–14% (48).

Systemic cancers are often accompanied by brain metastasis, a CNS complication which affects ~20% of adults with systemic malignancies (51). These most commonly include lung cancer, melanoma and breast cancer (51). Brain metastasis is becoming more apparent as awareness about it is increasing and diagnostic techniques are improving (42).

CNS is considered to be an immune-privileged environment and, to date, treatments for brain metastasis were based on stereotactic radiosurgery, whole-brain radiotherapy and other local therapies. However, increasing knowledge regarding the lymphatic system of the CNS and the alterations of the blood-brain barrier by the tumor microenvironment suggests that it is possible for immune cells to circulate in and out of the CNS (42). Consequently, it is currently considered possible to use ICIs to trigger peripheral T cells to exert antitumor effects within the CNS (49). This is supported by the association between the high density of TILs and OS in both primary tumors and brain metastasis (42).

The first ICI to exhibit efficacy in the treatment of brain metastasis was ipilimumab; this was discovered incidentally when patients treated for metastatic melanoma also presented with durable CNS responses (51). These results were subsequently confirmed during treatments of patients with melanoma brain metastasis using ipilimumab (51). Clinical data of these studies has demonstrated improvements in ORR, CNS disease control and response rate and PFS, establishing the basis for further ICI therapy. Additionally, anti-PD1 monoclonal antibodies nivolumab and pembrolizumab have exhibited similar efficacy for previously untreated melanoma brain metastasis (51).

On the other hand, in accordance with what has been previously observed in the treatment of melanoma and NSCLC, combined therapy exhibits the most promising CNS response rates to immunotherapy (51). In one of the studies aiming to demonstrate the efficacy of combination immunotherapy for untreated patients with melanoma brain metastasis, clinical outcomes of monotherapy using nivolumab were compared with those of combined therapy with Nivolumab and ipilimumab (51). The CNS response rates were higher when patients were treated with combined therapy (46%) compared with those observed following monotherapy (20%), which included CNS complete response rates of 17 and 12%, respectively (51). However, combination therapy was associated with high toxicity, with grade ≥3 AEs observed in 63% of patients receiving Nivolumab and ipilimumab, compared with 16% of patients receiving nivolumab alone (51).

Therefore, with promising clinical results for the treatment of brain metastasis, systemic immunotherapy contradicts the paradigm of the immune-privileged brain, especially with the use of combined therapy.

As aforementioned, a number of studies have reported that combination therapy of anti-CTLA-1 and anti-PD-1 antibodies is more efficacious compared with the respective monotherapies (48,50,51). However, the combination has also been demonstrated to increase the number and frequency of AEs (52). The most common AEs are cutaneous, including pruritus, rash and dermatitis; other AEs are gastrointestinal (mainly diarrhea and colitis), hepatic, endocrine (thyroid glands), pulmonary (most commonly pneumonitis), renal, pancreatic, neurological and rarely cardiac, including autoimmune myocarditis, heart failure, cardiomyopathy or cardiac fibrosis (52). The cardiac AEs are mostly documented among patients with history of cardiac pathologies, suggesting that these AEs represent a deterioration of existing cardiac disorders (52).

One potential cause of the apparent increase in AEs compared with each monotherapy may be the assessment of an optimal dosage regimen (53). In the treatment of patients with NSCLC, different outcomes were obtained when the administered doses of ICIs were adjusted (48). AEs may also arise from the tumor-affected organs, specifically as the disease progresses and the tumor undergoes biological changes (53). For instance, pulmonary events such as pneumonitis are more likely occur in patients with NSCLC compared with those with melanoma, whereas rashes or vitiligo are frequently observed in patients with melanoma (54,55). Notably, with the exception of endocrine events which are considered irreversible and hard to manage (53), most of the other AEs can be well managed and are reversible, especially with steroid co-treatment (54). A previous study has reported that following corticosteroid administration, a patient experienced a rapid increase in the ejection fraction that had been previously reduced to 15% due to of autoimmune myocarditis (52).

It remains unclear whether it may be safe to re-treat patients that presented with grade ≥2 irAEs with ICIs. Previous studies have reported that re-treating with ICIs is feasible, but often leads to the recurrence of grade ≥2 irAEs. Although no deaths were recorded, irAEs occurred on 22 out of 40 patients in one study that evaluated the effectiveness of rechallenging with ICIs after an irAE (55). Thus, re-administration of ICIs may be safe if patients are closely monitored, especially if these patients have previously achieved a complete or partial response prior to the first occurrence of an irAE in their initial treatment (56).

Assessing rechallenges remains specific to each case and to the risk-benefit ratio. For example, re-treatments may only be considered if the grades of the irAEs decrease to 0 or 1 (56). Treatment decisions also depend on the potential severity of irAE reoccurrence, especially if these are cardiac or neurological, as the tools for imaging and biological monitoring that allow estimations of future recurrence of irAEs are lacking for neurological irAEs (56).

Researchers are currently developing predictive biomarkers of treatment response, one of which is the tumor cell expression of PD-1 ligand 1 (PD-L1), which binds to the PD-1 inhibitory receptors on T cells (51,57). The use of predictive biomarkers may allow improved patient selection for treatment and may help predict the extent of the response to treatment using ICIs (57). For example, in one study, patients with NSCLC with PD-L1⁺ brain metastasis exhibited a higher intracranial response rate (29%) compared with no response for patients with PD-L1⁻ brain metastasis (51). In addition, the expression of PD-L1 differs with the type of cancer, and has been reported to be highest among patients with NSCLC and lowest in melanoma, where PD-L1⁺ cells were mainly non-tumor cells that were present in the tumor microenvironment (51). Furthermore, following treatment with CTLA-4/PD-1 checkpoint inhibitors, PD-L1 expression correlates with improved PFS and OS rates in NSCLC and renal cell carcinoma (57). However, PD-L1⁺ non-tumor cells exhibit a greater degree of response compared with PD-L1⁺ tumor cells (57). One explanation may be that macrophages and activated lymphocytes that express PD-L1 may interact with PD-1 inhibitory receptors on T cells, inhibiting their proliferative functions (57).

Therefore, numerous variables and conflicting data, including tumor type, identity of cells expressing PD-L1, various reagents and staining methods, as well as the incompatible cut-off points for determining positivity, complicate the use of PD-L1 as a predictive biomarker to assess the efficiency of treatment involving ICIs (57).

Another potential clinical biomarker for the detection and treatment assessment of brain metastasis is the tumor mutational burden (TMB). For instance, in one series of experiments, high TMB in brain metastasis was more common compared with that in primary tumors and was reported in 39% of the cases (51).

In conclusion, ICIs are a centerpiece of immunotherapy, as they exhibit antitumor activity across a range of tumor types. In addition, combined therapy with anti-CTLA-4 and anti-PD-1 antibodies results in higher rates of OS and PFS compared with those following monotherapies with either of the two ICIs. However, these high response rates are accompanied by a variety of irAEs, which are, in most types of tumor, reversible and manageable when steroids are administered. Rechallenging with ICIs following occurrence of irAEs is considered to be feasible if patients are closely monitored. Finally, further studies are needed to assess the predictive role of PD-L1 expression as a biomarker.

One form of adoptive cell transfer is TIL therapy, which enhances the function of the naturally occurring T lymphocytes; T cells infiltrating the tumor are harvested from the patient, activated and expanded, an infused back into the patient in order to destroy tumor cells (60).

Engineered TCR therapy is applied to patients whose T cells do not proliferate sufficiently to challenge the tumor (60). In this approach, T cells are harvested, activated, expanded and equipped with receptors that target specific cancer antigens that are protein, carbohydrate or glycolipid-based (60).

CAR T-cell therapy has the ability to target cancer cells even when their antigen is not bound to the surface of major histocompatibility complex (MHC) by equipping patient T cells with a synthetic receptor termed CAR (60). However, the range of potential antigen targets is limited, since CAR T cells only recognize antigens that naturally occur on cell surfaces (60). CAR T-cell therapy involves genetic modification of T cells harvested from patients with cancer in vitro to recognize a cancer-specific antigen (60). The engineering of T cells has exhibited potential in cancer therapy, especially in overcoming the limitations of TIL and TCR therapies of being unable to recognize cancer antigens unless they are expressed by MHC molecules (65). However, these modified cells do not undergo normal tolerance mechanisms, such as thymic education (60). In addition to their reactivity against target molecules, these cells may react against antigens present in healthy tissues (59). One potential solution for this toxicity is to modify the antigen specificity of T cells in a transient manner (59). Another strategy uses a drug-inducible suicide gene or a cell-expressed ligand that is targeted by a depleting antibody in order to allow the removal of donor T cells (59). In other approaches, the CAR activity depends on small molecule drugs, co-expression of two tumor antigens or non-expression of a non-tumor antigen (59). In addition, the use of a bi-specific antibody or a biotin-binding immune receptor in conjunction with a biotinylated molecule targeting a tumor antigen brings together lymphocytes and tumor cells, which may aid the selective and conditional antigen targeting (59).

NK cells have been incorporated in adoptive cell therapy by equipping NK cells with cancer-targeting CARs (66). NK cells are innate lymphocytes that recognize and lyse transformed or virally infected cells without prior activation (67). Adoptive cancer therapy with NK cells has been tested in clinical trials due to the ability of NK cells to induce antigen-independent immune responses against malignancies that are not restricted by the MHC (68). Allogeneic NK therapy has an advantage against autologous T cell ACT due to a favorable therapeutic and safety profile, suggesting that NK cells may be a suitable alternative for CAR-based therapies (69). Cancer treatment-induced immune defects associated with the use of patient-derived immune cells may be avoided by using NK cells obtained from healthy donors (68). In addition, NK cells recognize cancer cells and trigger tumor lysis by expressing various endogenous activating receptors (68). CAR-expressing NK cells function even when the CAR target antigens are downregulated in cancer cells during treatment (68). Additionally, in contrast to T cells, NK cells do not produce autocrine growth factors such as IL-2, which limits their lifespan; therefore, NK cells do not remain in circulation, reducing the risk of long-term AEs and eliminating the need for introducing suicide genes (68). NK cells have also been reported to not induce graft-versus-host disease or other types of alloimmune or autoimmune toxicity, allowing versatile cellular immunotherapy with allogeneic NK cells from healthy donors (68).

Several factors appear to be important for the effectiveness of ACT therapy including cell dose, cytolytic effector function and the long-term persistence of transferred cells (70). The latter is associated with a minimal differentiated phenotype, which maintains the capacity of producing a continuous supply of cytolytic effector progeny (70). The quality of the transduced cells that are administered to the patient is also of great importance, and this area has been extensively studied (70). Lowering the dose of IL-2 added to the cells and reducing the time that the transduced cells spend in culture (between 5 and 7 days) has been demonstrated to provide promising results, as the culture conditions may induce strong dependence on cytokines (70).

Naïve rather than central memory T cells give rise to an effector progeny with improved antitumor immunity following ACT (71). Effector cells derived from naïve T cells lose the expression of the central memory cell marker L-selectin more rapidly compared with those derived from central memory T cells, but do not acquire the expression of killer cell lectin-like receptor G1, which is a marker for terminal differentiation and replicative senescence (71). Thus, naïve-derived cells exhibit high proliferation and cytokine production following ACT (71). These results suggest that superior efficacy of ACT is obtained by insertion of genes that confer antitumor specificity into naïve T cells compared with central memory T cells (71).

The terminal differentiation status of transferred T cells and their low-affinity binding to tumor-associated antigens (TAAs) limit the effectiveness of patient-derived tumor-specific T cell ACT (72). TAAs are expressed in healthy tissues a low level (72). Transgenic TCRs or CARs recognize TAAs with high affinity and without MHC restriction, resulting in cytotoxic T cell activity against the tumor (72). However, a high risk of targeting healthy self-tissues occurs when central tolerance is overlooked. In order to achieve the greatest efficiency on tumors with the lowest risk of off-target and side effects, the choice of the TAA and of the TCR affinity is crucial (72).

Following transplantation into patients, infused T cells become functionally fatigued, and consequently their efficiency decreases (70). CD8⁺ T cells lose their antitumor efficacy as they produce IFN-γ, which activates the innate and adaptive immune response (73). This limitation may be resolved by the adoptive transfer of tumor antigen-specific stem cell memory T (TSCM) cells (73). TSCM cells are similar to naïve T cells but are also highly proliferative, exhibit a long lifespan and produce numerous effector T cells following antigen stimulation (73).

T cell-T cell interactions enhance the function of T cells within hours of molecular (antigen) stimulation (70). Enhanced cell motility is a short-time consequence of molecular stimulation, leading to aggregation and further activation (70). Functional activation of T cells is halted in the absence of T cell-T cell interactions even when continuous molecular stimulation is performed (70). Cryopreservation of the cellular product to perform lot release testing studies, followed by direct reinfusion to patients after conditioning chemotherapy is standard practice of CAR or TCR T cell therapy (70). An intermediate step of short-term ex vivo culture with molecular stimulation to induce T cell-T cell interactions may be favorable and result in more functional cells reinfused to the patients (70).

Compared with other immunotherapies, ACT has certain advantages, including T cell populations having optimal recognition of autologous tumor antigens that can be preferentially isolated ex vivo for therapy (74). These selected T cells can be expanded to large numbers under in vitro conditions that overcome tolerizing factors within the tumor microenvironment. In addition, regulatory and immunosuppressive factors can be eliminated by conditioning the host prior to cell transfer.

Since single-agent monotherapies are continuously proving futile, combination therapies utilizing two or more types of ACT or combinations of ACT and cell-based therapies have exhibited promising potential in the treatment of cancer such as melanoma (74). Traditional melanoma treatment includes the use of the chemotherapeutic agent dacarzabine, which exhibits a modest patient response of 10–20% with a complete response rate <5% (74). Our previous studies have investigated the use of anthrax lethal toxin in murine models as a potential therapeutic agent for this disease and elaborated on the cellular mechanisms involved in the inhibition of Tregs (75).

In combination therapy, the use of TIL with high-dose IL2 generated a clinical response rate of 55%, in which T cell-mediated tumor regression was observed (76). Additionally, T cell-based therapies that involve the co-delivery of cytokines such as IL-12, IFN-α, IFN-γ and TNF-α have enhanced the patient response (77). Other types of cancer such as glioblastoma multiforme (GBM) have been reported to respond to similar therapies. For example, our previous studies investigated the use of metformin, a biguanide agent used to treat type 2 diabetes mellitus, as well as human recombinant arginase I (Co)-PEG5000 [HuArgI (CO)-PRG5000] for the treatment of GBM (78,79). In the context of immunotherapy, CAR T cell-based approaches in combination with radiotherapy exert synergistic efficacy in GBM (77).

EBV-induced lymphoma can be effectively treated with ACT therapy that restores anti-EBV immunity using viral-antigen-specific T cells (80). Repetitive in vitro stimulation of peripheral blood lymphocytes (PBLs) with EBV-B lymphoblastic cell lines has been used to generate lymphocyte cultures highly enriched for EBV-antigen-specific T cells that are suitable for ACT therapy and inhibit EBV-induced lymphoproliferation (80).

ACT therapies exhibit limited success in treating tumors that do not express viral antigens due to the difficulty in generating tumor-antigen-specific cells (80). One review that surveyed clinical trials involving non-specific activated lymphocytes or non-specific PBLs activated in vitro with anti-CD3 reported a low response rate for this therapy, suggesting the necessity of using tumor antigen-specific lymphocytes in ACT (80).

Tumor recurrence is observed when cytotoxic T cell responses are inhibited by a subset of TGFβ-responsive squamous cell carcinoma stem cells which evade immunotherapy via the expression of CD80, a co-stimulatory molecule involved in T-cell activation and the activity of normal and malignant B cells (81). Tumor-initiating stem cells (tSCs) possess self-renewal and differentiation capacities (81). These cells fuel and sustain tumor growth by overcoming the immune surveillance barrier (81). The ability of a regressed tumor to regrow implies that at least a number of tSCs acquire the ability to resist the enhanced antitumor immunity (81). One hypothesis is that tSCs exhibit limited antigen presentation and are therefore undetectable by the immune system (73). Alternatively, tSCs may be able to avoid immune attacks due to their antigen-editing, independent molecular features (82). These tSCs may become invasive in response to enriched TFGβ around the vessels; they are also more tumorigenic than tSCs distant from blood vessels, which do not receive a TGFβ stimulus (82). TGFβ-responding tSCs survive chemotherapy and induce tumor relapse (83).

An effective mouse ACT model was established in a previous study, in which skin squamous cell carcinoma (SCC) tSCs were tracked, and their susceptibility was directly determined and compared with antigen-specific antitumor immune responses (81). The results demonstrated that TGFβ-responding tSCs exhibited resistance to cytotoxic T cell responses and were responsible for tumor recurrence following ACT therapy (81). In addition, the aforementioned study demonstrated that within the tumor, these stem cells expressed the immune cell ligand CD80, the silencing of which diminished their resistance to immune surveillance and weakened tumor relapse (81).

ACT is an effective cancer treatment, but it also has severe side effects. The variation and severity of these side effects vary depending on the patient health prior to treatment, the type and stage of cancer, as well as the type of T-cell transfer being used (84). The toxicity is observed as a result of direct T-cell attacks on normal tissues, i.e., autoimmunity (85). However, a number of normal tissues tolerate a certain degree of autoimmunity, and effective targeting of the antigens by these cells is still possible (85).

In CAR T-cell therapy, cytokine release syndrome is a side effect defined by the release of large amounts of cytokines into the blood, which ultimately leads to fever, chills, difficulty breathing, nausea, tachycardia, fatigue and muscle pain (84). Treatment with the monoclonal antibody tocilizumab is used to control this side effect (86). In addition, allergic reactions to CAR T cells have been recorded in a number of patients; the symptoms of allergic reactions include fever, difficulty breathing and chills (86). Increased risk of infection is observed as a side effect of certain types of CAR T-cell therapy when treating leukemias and lymphomas (86). The increased risk of infection occurs due to the recognition by CAR T cells of CD19, which is expressed on the surface of B cells; the CAR T-cells destroy the CD19⁺ B cells, leading to a decreased ability to fight infections (86). Immunoglobulin therapy is used to treat this side effect by administering antibodies to help fight infections (86).

TIL therapy causes capillary leak syndrome that is characterized by the leak of fluid and proteins out of small blood vessels into the surrounding tissues, leading to severe low blood pressure, which may lead to multiple organ failure (84). Neurological side effects that affect the brain have also been observed, and the symptoms include headaches, altered consciousness, speech changes, seizures and confusion (86). In addition, severe rashes leading to vitiligo occur in certain patients (86). A number of patients experience uveitis with impaired vision and decreased hearing, possibly due to autoimmunity against pigmented cells in the stria vascularis of the inner ear (85). These toxicities respond well to topical corticosteroids (85). In addition, hepatotoxicity has been observed in certain patients with renal cancer, as well as severe diarrhea in patients with colorectal cancer (85).

DNA vaccines are usually bacterial plasmids containing genes encoding tumor antigens coupled to CMV promoters (89). These vaccines aim to induce an innate immune response that augments the adaptive immune response towards the tumor presenting these antigens (89). Thus, DNA vaccines aim to boost the production of T cells such as CD8⁺ and CD4⁺ cells that specifically target the tumor (5). Another aim of DNA vaccines is breaking immune tolerance and inducing an immune memory, especially in the cases where a DNA vaccine is used to prime the T cells against the antigen to improve the benefits of other therapeutic techniques (1). In the case of DNA vaccines, the DNA sequence may be engineered to improve protein expression, for instance by replacing the leader sequence with other sequences and adding immunoglobulins as well as performing codon and RNA optimization (5). In addition, a novel technique that has emerged recently in DNA vaccines and provides hope for cancer vaccination is synthetic consensus vaccines that rely on generating consensus DNA sequences based on comparing the native sequences between various species; these synthetic consensus sequences are able to break immune tolerance due to the increased diversity compared with that of the native sequences (5,90). DNA vaccines can also be used in combination with other therapies to overcome certain limitations. ICIs targeting PD1 and CTLA4 have been demonstrated to enhance the antitumor activity of a DNA vaccine against mastocytoma by boosting its antitumor immunity, leading to a ≤90% survival rate (91). A previous clinical study has also investigated the therapeutic effects of combining DNA vaccines with cytokines such as IL-2 and IFN-γ (88). In addition, the use of DNA vaccines is supported by the fact that intrinsic unmethylated CpG islands in the bacterial plasmid function as an adjuvant, thus stimulating the immune response to the vaccine (92). To determine the most effective combination of treatments and DNA vaccines, assessment of the tumor microenvironment as well as cells involved in the immunosuppressive behavior in that niche should be performed (93).

The mode of delivery should be taken into consideration when discussing the cellular mechanisms of DNA vaccines. DNA vaccines can be delivered through a variety of different routes including intramuscular, subcutaneous, mucosal or transdermal delivery (94). In addition, it is important to ensure that the plasmid transfects the cells, for which electroporation may be used (94). Furthermore, when the vaccine infects the cell, the plasmid is replicated in the cell, which is driven by the eukaryotic CMV promoter to produce that target antigens; following production of the antigens, they are then expressed in MHC class I and II, which are recognized by various immune cells and are capable of producing humoral and cellular immune responses (5).

The advantages of using DNA vaccines include their low cost, ability to elicit antigen-specific immune responses, easy sequence alteration, large-scale production and storage (93). In addition, DNA vaccines are not infectious and do not cause diseases or elicit immune responses in individuals of a specific MHC class (93). Therefore, in contrast to personalized vaccines, DNA vaccines may be considered versatile (93). Finally, as these antigens are expressed in the cells, they undergo post-translational modifications that form proteins similar to the host proteins, which ensures appropriate immune presentation (94).

On the other hand, certain disadvantages associated with DNA vaccines have been reported. DNA vaccines are negatively charged due to their DNA base and have a low molecular weight, which may cause difficulty in cellular uptake and poor antigenic production, leading to poor immune responses (92). Additionally, challenges occur in selecting the appropriate tumor antigen and combating the problems of poor immunogenicity and immunosuppressive microenvironments, which may lead to weak results in this field (95).

The only DNA cancer vaccine that has reached a phase III clinical trial is VGX-3100, which is a DNA vaccine targeting precancerous lesions that may progress to cervical cancer, termed CIN2/3 (96). This vaccine appears to elicit durable responses, but has not yet been approved by the FDA (96). In addition, DNA vaccines have been studied for breast, prostate, cervical, ovarian and pancreatic cancer, glioblastoma, melanoma, renal cell and urothelial carcinomas, but no significant progress has been reported beyond phase II clinical trials or even preclinical animal models (97).

Peptide vaccines consist of nongenetic components of the disease to be treated, such a tumor or an infectious agent, in order to elicit an immune response (98). Peptide vaccines do not unnecessarily overload the immune system, as only the epitope of interest is delivered to the immune system of the individual (99). These vaccines are also cheap and can be easily produced (99). However, they usually fail to elicit an immune response due to the presence of immunosuppressive molecules in the tumor microenvironment (100), and the safety of these vaccines when combined with adjuvants remains unclear; thus, the safety of usage of adjuvants should be assessed and eliminated in order to ensure the efficacy of peptide vaccines (99). Therefore, current research aims to improve peptide vaccines. For example, peptide vaccines may be potentiated by combination with other molecules, such as avasimibe, a molecule that aids in cholesterol metabolism and increases the potentiation of a Kras vaccine targeting lung tumors (101), indomecathin, which reduces the rate of proliferation in tumor cells and increases the apoptotic rate when used in conjunction with a MUC1 peptide vaccine (100), or by adding adjuvants as the antigens by themselves provide low immunogenicity and MHC restriction (102). Future research is required to enhance the immune response in other manners such as utilizing protein nanoparticles that surround the peptides, which is an approach that offers numerous merits including a symmetrical structure, biodegradability and an appropriate size for the delivery of vaccines (103).

One FDA-approved vaccine that is not strictly a peptide vaccine, but may be considered to be one, is IMLYGIC or T-VEC, which is a modified herpes simplex virus 1 that replicates in the lesions of patients with recurrent melanoma, causing cell lysis and death (104). The reason why it may be considered a peptide vaccine is that this virus is engineered to express the granulocyte-macrophage colony-stimulating factor, which promotes the antitumor response and priming of T cells (104).

DCs were first described by Robert Steinman in 1973 due to their unique shape and high MHC expression (105). DC vaccines are vaccines produced by harvesting patient DCs and transfecting them with the tumor antigen ex vivo; these cells are then re-introduced into the patient's body which can usually occur via many routes including intradermal, intravenous, intranodal and intralymphatic routes, to destroy the tumor cells that they readily recognize (106). DCs possess an ability to modulate adaptive immune responses, which renders them as potent stimulatory tools for memory and immune cells (91,106). In addition, DCs stimulate naïve T cells (106). However, DCs are low in number in the peripheral blood and tissues, and thus, their population needs to be enhanced in vivo or ex vivo prior to vaccine administration (107). The advantages of DC vaccines include their personalized nature, the feasibility of producing an immune response since dendritic cells are major players in the activation of adaptive responses, their ability to specify the response towards one antigen or a group of antigens and the relatively safety in individuals as they do not cause AEs (108). By contrast, DC-based vaccines, similar to other vaccines, face certain hurdles, such as tumor immunosuppression and the limited functions of monocyte-derived dendritic cells, which are the cells used to generate this type of vaccines (109). In addition, since they are personalized, DC vaccines tend to be expensive (109). As with other types of vaccines, DC vaccines suppress tumor growth and increase the number of T cells infiltrating the tumor microenvironment, which can be more efficient compared with other types of vaccines in certain cases, such as in murine lung carcinoma (LL2), the study was done in vitro and the DC vaccine was able to exhibit superior immunogenicity compared with an antigen-adjuvant vaccine (102). Furthermore, DC cancer vaccines may also be used with other treatments for enhanced results, including ICIs such as anti-PD-1 and adjuvants (110). Using a mathematical model, Lai and Friedman (111) have demonstrated a synergistic effect of the combination of a DC cancer vaccine and anti-PD1 in cancer therapy. In laboratory preparation of DC vaccines, observing and controlling culture conditions is crucial since DCs are highly sensitive to their environment (110). Particular care should be taken in identifying the molecules that allow efficient delivery of DC cells to the lymph nodes for maturation (110).

One example of an FDA-approved DC cancer vaccine is Sipuleucel-T or PROVENGE, which is used in the treatment of metastatic castration-resistant prostate cancer with metastasis beyond the prostate gland that cannot be treated by hormone therapy (112). DC vaccines for other types of cancer have not been approved; however, current efforts are aimed towards metastatic melanoma, breast and prostate cancer (113).

Whole-cell cancer vaccines contain whole tumor cells that have been modified ex vivo (114). Despite the lack of strong results in cancer vaccination, whole-cell vaccines offer numerous advantages. One advantage is that whole-cell vaccines express both tumor-specific and tumor-associated antigens (114). Additionally, whole-cell vaccines elicit strong cellular as well as humoral immune responses (114). However, tumor cells possess immune evasion strategies, which must be considered when modifying tumor cells to achieve adequate immunogenicity (115). In addition, whole-cell vaccines have not elicited strong immune responses in clinical trials, possibly because advanced tumors build immune tolerance that hinders immune recognition (114). Whole-cell vaccines are also time consuming, laborious and costly due to the numerous procedures needed to acquire, maintain, manipulate and reintroduce tumor cells to the individual (108). Carbohydrate antigens in the context of whole-cell vaccines are also important as they are expressed on the surface of cells in the form glycoproteins, proteoglycans and glycolipids, and are necessary for various biological processes including aberrant processes implicated in carcinogenesis (116). Xia et al (116) have developed a glycol-antigen microarray to study antibody responses to carbohydrates induced by whole-cell vaccines and reported high IgG and IgM responses induced by the GVAX pancreatic cancer vaccine, indicating the importance of other types of antigens in addition to peptide antigens (116). In terms of combination therapy, one study by Chen et al (117) has reported that combining a whole-cell breast cancer vaccine with the standard chemotherapeutic alkylating agent cyclophosphamide increases the clinical benefits of this agent in treating Her2⁺ metastatic breast cancer.

Cancer vaccination has been a potent field of research for the treatment of cancer in the past 30 years (88). Cancer vaccines can be used in two different manners: A prophylactic application that aims to prevent disease or as vaccine-mediated postoperative immunotherapy for recurrent and metastatic tumors. One major challenge for cancer vaccines is the interpatient variability of cellular responses, which causes a robust immune response in certain individuals, but no response in others (88). Another challenge is that cancer vaccines by themselves may not be efficient and require prior priming or co-priming of the immune system using other substances that potentiate the vaccine (101,102,118). In addition, limited knowledge is currently available on the intracellular processing and tracking in humans as opposed to animals due to ethical concerns (88). However, despite these drawbacks, cancer vaccines may have positive inclinations in the future, especially when combined with other types of treatment (88).

Antibodies are proteins engineered to target an epitope present on cancer cells (when used for immunotherapeutic purposes) and are produced, collected and administered to a patient and they circulate throughout the body until they meet the aforementioned antigen. They recruit other immune system agents to eliminate the antigen via three main mechanisms: Activating antibody-dependenT cellular cytotoxicity (ADCC), blocking growth factor (GF) receptors, and activating complement-dependent cytotoxicity (CDC) by complement activation (Fig. 1) (120). Understanding the mechanisms by which mAbs work must precede their application to ensure efficacy.

For activating ADCC, a specifically designed mAb attaches to a previously specified antigen and allows NK cells to recognize and eliminate it by releasing cytotoxic agents, which kills the cell by apoptosis (121,122). Targeting GF receptors is achieved by using several mAbs to competitively inhibit these receptors (123). For instance, targeting epidermal growth factor receptor blocks its use, causing the internalization and downregulation of the receptor (123). In CDC, a mAb binds to antigens on the targeT cell surface and triggers multiple pathways in the complement cascade, where complements (various soluble plasma proteins and membrane proteins) bind to the mAbs, induce an attack and lead to the lysis of the targeted cell (124).

There are three types of mAbs that are used in cancer treatment: Naked, conjugated and bi-specific. Naked mAbs are used without any drugs (125). For example, rituximab induces tumor cell death through the dependent and independent mechanisms centered on Fc (125). The dependent mechanism contains the aforementioned ADCC mechanism mediated by NK cells and macrophages, antibody-dependenT cellular phagocytosis mediated by macrophages and CDC (125). Apoptosis is directly induced by the independent Fc mechanisms by the binding of a mAb to its receptor or by its blocking of receptor-ligand interactions, as is the case with the HER2 receptor-mediated GF signaling on cancer cells (126). Conjugated mAbs are tools through which chemotherapeutic agents and radioactive molecules are led directly to targeted cells (125). The conjugation of mAbs with radioactive substances, such as iodine-131 or yttrium-90, generates cytotoxic molecules, such as monomethyl auristatin E or emtansine, improves efficacy compared with that of naked mAbs and generates antibody-drug conjugates (125). This facilitates the delivery of cytotoxic agents to tumor cells, increasing their efficiency (126). Bispecific (or bifunctional) mAbs are a type of mAbs in which two IgG chains of different specificity are amalgamated; they can be administered to effectively bind two different surface antigens, which eases the burden of the patient significantly by decreasing the frequency with which this procedure is administered (127).

mAb monotherapy has been successful in treating certain patients with cancer, but current studies are shifting towards combining mAb with other antitumor therapies for a more effective treatment: mAbs and ICIs (128,129). The effect of the mAb cetuximab in treating head and neck squamous cell carcinoma appears to be enhanced when combined with inhibitors of the immune checkpoint PD-1/PD-1L such as anti-PD-1 antibodies and pembrolizumab (128). In addition, resistance to the monotherapy of the mAb trastuzumab in advanced HER2⁺ breast cancer may be overcome with the use of pembrolizumab (129).

In addition to immune checkpoint blockage, cytokine immunotherapy is also synergistic with monoclonal antibody therapy. An engineered PEGylated IL-2 is currently undergoing clinical trials in which it is combined with the mAb Nivolumab for the treatment of advanced solid tumors (130). PEGylated IL-2 has also exhibited potential therapeutic advantage when combined with the mAb Atezolizumab in treating NSCLC (131).

There are several side effects for mAb treatments against cancer. In one case, upon treating 496 patients with metastatic melanoma with anti-PD1 antibodies, 242 side effects were described in 138 patients, including skin, gastrointestinal and renal system side effects, and, in certain cases, rare side effects including diabetes mellitus and pancreatitis (23). In addition, in patients with melanoma treated with Nivolumab or pembrolizumab, side effects were observed in the respiratory tract, musculoskeletal system, nervous system, eyes, heart and blood (132).

As far as the future of monoclonal antibodies is concerned, this technology may improve the current shortcomings in cancer therapeutics. mAbs possess specificity for certain conformations to ensure improved selectivity and fulfillment of therapeutic goals. However, the most prominent limitation currently is that the majority of mAbs are unable to recognize 3D configurations. Thus, 3D-recognizing antibodies may be valuable to offer an extra level of neutralization.