The recent discovery of the molecular structure of tumor antigens expr
essed by melanoma cells has contributed to the development of therapeu
tic strategies aimed at stimulating anti-tumor immunity, The first cli
nical trials in patients with cancer involved systemic administration
of interleukin 2 alone or in combination with alpha-interferon or othe
r chemotherapy agents. Objective clinical responses were observed in 1
5 to 25% of the patients with melanomas or renal cell cancer, In order
to improve these encouraging early results, different-clinical protoc
ols are being evaluated with the goal of increasing intra-tumoral conc
entrations of the administered cytokines. Better optimization of metho
ds for immunizing against specific tumor antigens naturally leads to t
he transition from non-specific stimulation of the human immune system
to tumor antigen specific immunotherapy.