IMMUNOTHERAPY
The term immunotherapy
in relation to cancer refers to processes that manipulate the immune system to
improve the body’s response against a tumor. Immunotherapy has a long history
and began in the era before the advent of cytotoxic drugs when cancer patients
were treated with Coley’s toxin. This contained a mixture of killed Streptococcus pyogenes and Serratia marcescens bacteria that
stimulated the immune system nonspecifically . The BCG vaccine, which contains
killed mycobacteria, was used in the 1960s and 1970s, to treat malignant
melanoma and has since been used to treat bladder cancer. Mycobacteria are
potent stimulators of the immune response and increase the production of
several cytokines, including interferon γ (IFN- γ) and tumor
necrosis factor α (TNF- α). Nowadays, recombinant
cytokines may be given directly to enhance the immune response. For example,
interferon α (IFN- α) has been used successfully to
treat multiple myeloma, CML, hairy cell leukemia and malignant melanoma.
Interleukin 2 (IL-2) appears to exert an anticancer effect through the
prolonged stimulation of Natural Killer cells; it has been used to treat renal
cancer and malignant melanoma .
An exciting development in immunotherapy has been the
production and clinical trials of a number of anticancer vaccines based on
tumor associated antigens. Examples include vaccines based on peptides derived
from carcinoembryonic antigens, and the BiovaxID™ vaccine for the treatment of
follicular lymphoma, a type of nonHodgkin’s lymphoma involving B lymphocytes.
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