The hypothesis of immunologic surveillance of neoplasia is predicted on the
theory that the immune system is capable of discriminating self from forei
gn antigens, and that tumour-specific antigens are regarded by the immune s
ystem as nonself. An alternate view proposed was that the immune system has
evolved to detect danger by employing 'professional' antigen-presenting ce
lls as sentinels of tissue distress.
The field of tumour immunology has witnessed short bursts of great exciteme
nt followed by longer periods of pessimism. Enthusiasm appears to be rising
again as many tumour-associated antigens have been identified and their us
e in vaccines is currently the subject of many clinical trials. The develop
ment of genetic engineering has allowed the conversion of anti-tumour mouse
monoclonal antibodies into mouse-human chimerized antibodies and humanized
reagents, which are undergoing clinical trials. Although 'immuno-genethera
py' appears to be a promising approach, much work still needs to be done to
understand the mechanisms involved so that efficacious treatment modalitie
s can be designed.