In vitro studies and animal experiments have demonstrated the reality
of physiological immune responses against tumors. Interleukin-2 was th
e first immunological agent which demonstrated an anti-tumor effect by
activating immune effecters. In vitro IL2 may generate lymphokine act
ivated killer (LAK) cells from peripheral blood lymphocytes or tumor i
nfiltrating lymphocytes (TIL) expanded from tumor. In melanoma and ren
al cell carcinoma, IL2 alone, or associated with LAK cells or TIL, ind
uces clinical responses. However, its clinical efficacy is associated
with some toxicity related to a capillary leak syndrome. This implies
an improvement in the selection of patients and in the understanding o
f IL2 action. Future directions in immunotherapy include combination o
f IL2 with other cytokines, monoclonal antibodies or chemotherapy. Cyt
okine gene therapy is designed to introduce IL2 or other cytokine gene
s into tumors to reduce systemic toxicity and to achieve high local cy
tokine concentration. Animal models and the first human trials make th
is approach promising.