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4.6 Cancer vaccine     97





































                  FIGURE 4.13  Main strategies in cancer vaccine production.

                     It would be worthy to illustrate divergent strategies in the way of cancer vaccine
                  production. In spite of ancient infectious prohibition vaccines with the purpose of
                  prevention, cancer vaccines are on the basis of triggering the immune system, promi-
                  nently the CD8 + T cell in order to combat the cancer [73].

                  4.6.1.1  Dendritic cell vaccine
                  Dendritic cells control the activity of B cells and T cells, by moving and migrating to
                  lymphatic organs and by secretion of cytokines, they ignite immune responses [79].
                     From the aforementioned information, DCs have considered to be one of the
                  most useful APCs, that could help the sensitization of MHC restricted T cells to
                  commence the immune responses [79,80]. To illustrate the functional ability of DCs
                  in cancer vaccination it is not necessary to mention that tumor has the ability to sup-
                  press the maturity and trigger apoptosis of body DCs. DCs vaccines are exogenous
                  APCs which could compensate the tumor suppression effect and motivate specific T
                  cells recognizing tumor antigens [73].
                     In 1995 the first DC vaccine prepared for clinical trial on patients with meta-
                  static melanoma, patients were administrated with APCs along with nanopeptide of
                  MAGE-1 [81].
                     Some other investigation on DCs transfecting with tumor RNAs and DNAs, these
                  vaccines have shown immunogenic responses [82-84].
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