Table 1.
Approach | Action Mechanism | Reference |
---|---|---|
1. To stimulate effector immune values | ||
Vaccines | Stimulates the immune system of the host | (Farkona et al., 2016) |
Cytokines | Either directly exerting an antitumor effect or indirect improving the antitumor immune response | (Disis, 2014) |
Adoptive cellular therapy | By inducing a set of high avidity effector T cells and overcoming tumor antigen tolerance | (Farkona et al., 2016, Mellman et al., 2011, Disis, 2014) |
Oncolytic virus therapy | To treat cancer, existing biological agents are being used. Despite the lack of initial virulence, genetically engineered viruses can infiltrate and lyse cancer cells. | ((Dobosz and Dzieciątkowski, 2019, Disis, 2014). |
2. To inhibit the immunosuppression mechanism | ||
Immune checkpoint blockade | ||
Monoclonal antibodies against CTLA-4 | Reactivates pre-existing antitumor T cell responses, which might be useful in cancer therapy and might initiate new | (Farkona et al., 2016) |
Antibodies against PD1 and PD-L1 | New Sufficient clinical reactions are triggered, which are frequently long-lasting | (Farkona et al., 2016) |
CTLA-4 = Cytotoxic T-lymphocyte–associated antigen 4.
PD-L1 = Programmed cell death ligand 1.