Malignant tumors express antigens that may stimulate and serve as targ
ets for antitumor immunity. Virally induced tumors usually contain int
egrated proviral genomes in their cellular genomes and often express v
iral genome-encoded proteins that may stimulate specific host immune r
esponses. Antigens unique to individual tumors that stimulate specific
rejection of transplanted tumors have been demonstrated only in exper
imental animals. Other tumor antigens that potentially can stimulate i
mmune responses are shared by different tumors. These include products
of mutated or rearranged oncogenes or tumor-suppressor genes. Tumors
may also overexpress tissue differentiation antigens or embryonic anti
gens, which also have the potential to be recognized by the immune sys
tem. The recent identification of tumor antigens recognized by cytotox
ic T cells opens up new possibilities for constructing chemically defi
ned antigens for specific immunotherapy. Treatment of malignant tumors
in humans by immunologic approaches, although theoretically attractiv
e, has not yet succeeded on a large scale. Important progress in immun
otherapy of cancer is emerging with several different treatment modali
ties.