Mathematical models analyzing tumor-immune interactions provide a framework by which to address specific scenarios in regard to tumor-immune dynamics. Important aspects of tumor-immune surveillance to consider is the elimination of tumor cells from a host's cell-mediated immunity as well as the implications of vaccines derived from synthetic antigen. In present studies, our mathematical model examined the role of synthetic antigen to the strength of the immune system. The constructed model takes into account accepted knowledge of immune function as well as prior work done by de Pillis et al. All equations describing tumor-immune growth, antigen presentation, immune response, and interaction rates were numerically simulated with MATLAB. Here, our work shows that a robust immune response can be generated if the immune system recognizes epitopes that are between 8 to 11 amino acids long. We show through mathematical modeling of how synthetic tumor vaccines can be utilized to mitigate a developing cancer.utilized mice that were inoculated with chemically-induced cancer cells; such cells lacked the capability to metastasize within a host. Over time, this led to the development of cancer-specific immunity in the recipient mice. This discovery provided the evidence needed for Ehrlich's hypothesis. Such experiments demonstrated that it is essential to have the presence of an antigen to elicit an immune response in the host, because if no distinctive structures exist, then no recognition would be established [9]. F. Macfarlane Burnet and Lewis Thomas, well-known immunologists during the 20 th century, hypothesized that for immunosurveillance to exist, lymphocytes would need to act aggressively akin to sentinels to recognize and eliminate a cancer threat. The cancer immunosurveillance theory revolves around three transitions states, denoted as "E's" [9]:• Elimination-The establishment of a strong cancer surveillance network by both the innate and adaptive immune system that seeks to eliminate cancer populations.• Equilibrium-The long-term process of combat between a cancer population and a host's immunosurveillance network.• Escape-The overpowering of cancer surveillance network by strong tumor variants, which results in host death.