Figure 1. Residual infiltrating tumor cells after standard of care treatments may be eliminated by tumor-specific T cells stimulated by immunotherapies, such as gene-mediated cytotoxic immunotherapy (GMCI).

Standard of care treatment for newly diagnosed GBM includes surgical resection followed by radiation and temozolomide chemotherapy. However, progression occurs in more than two thirds of patients within 1 year due to growth of residual, infiltrating tumor cells. Immunotherapies may increase the efficacy of the immune system to fight against this minimal residual disease. GMCI involves injection of AdV-tk to the tumor bed at the time of surgery followed by oral valacyclovir prodrug administration to induce immunogenic tumor cell death. Surgery, radiation, and the viral vector stimulate infiltration of antigen-presenting cells (APC). Tumor-associated antigens (TAA) are presented by MHC class I and II molecules on APCs stimulating tumor-specific CD4 and CD8 T cells. The HSV-tk protein expressed from the AdV-tk vector has a superantigen-like effect that further stimulates proliferation of T cells. Thus, the approach generates an antitumor vaccine effect that may compliment standard of care to improve outcomes for patients with GBM.