Page 97 - Bio Engineering Approaches to Cancer Diagnosis and Treatment
P. 97

4.6 Cancer vaccine     95












































                  FIGURE 4.12  Schematic of cancer vaccine function or release of tumor cell antigen as a
                  result of cancer cell death.

                  advanced. Moreover, immunotherapy has seen tremendous growth by demonstrating
                  that T cells can show tumor suppression and antitumor activity. Tumor cells typically
                  express mutated proteins or normal proteins in a higher rate which cause them to be
                  recognized by CTLs (cytotoxic T lymphocytes) [71].
                     Schematic of cancer vaccine function (or release of tumor antigens as a result of
                  tumor cell death) are shown in Fig. 4.12. Firstly, APCs (DCs, neutrophils, lymphatic
                  endothelial cells, and macrophages) must recognize the antigen, then the T cells need
                  to be activated by APCs, and in the last stage activated T helpers as well as T cyto-
                  toxic must move to the tumor site and change the immunosuppressive microenviron-
                  ment to an inflammatory condition. This alteration in the tumor microenvironment
                  helps the cytotoxic T cells to fight against T cells [70].
                     First, by vaccine administration or tumor antigen release APCs recognize tumor
                  antigens and represent them on their surface, then they migrate into Lymph node and
                  cause T cells differentiation and proliferation. Afterwards, mature T cells go through
   92   93   94   95   96   97   98   99   100   101   102