Immunotherapy of mice with preexisting cancers with heat shock protein
preparations derived from autologous cancer resulted in retarded prog
ression oi the primary cancer, a reduced metastatic load, and prolonga
tion of life-span. Treatment with heat shock protein preparations deri
ved from cancers other than the autologous cancer did not provide sign
ificant protection. Spontaneous cancers (lung cancer and melanoma), ch
emically induced cancers (fibrosarcoma and colon carcinoma), and an ul
traviolet radiation-induced spindle cell cacinoma were tested, and the
results support the efficacy of autologous cancer-derived heat shock
protein-peptide complexes in immunotherapy of cancers without the need
to identify specific tumor antigenic epitopes.