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Immunologic approaches to the treatment of human cancer based on a guinea pig model
Authors:B. Zbar  E. Ribi  M. Kelly  D. Granger  C. Evans  H. J. Rapp
Affiliation:(1) Biology Branch, National Cancer Institute, National Institutes of Health, Public Health Service, U.S. Dept. of Health, Education and Welfare, 20014 Bethesda, Maryland, U.S.A.;(2) Rocky Mountain Laboratory, National Institute of Allergy and Infectious Disease, U.S. Dept. of Health, Education and Welfare, 59840 Hamilton, Montana, U.S.A.;(3) Department of Medicine, Strong Memorial Hospital, Rochester, 14620 New York, U.S.A.
Abstract:Summary Local immunotherapy is a form of cancer treatment where exogenous antigen is introduced into the area of the tumor. Under favorable circumstances, the perfused tumor regresses, systemic tumor-specific transplantation immunity is augmented, and distant microscopic metastases regress. Successful local immunotherapy requires an immunologically competent host, small tumor burden, and tumor located usually in the skin. A wide variety of biologic agents are capable of promoting local immunotherapy. BCG has been most widely studied. The antitumor activity of two different preparations of the Tice substrain of BCG were compared. No significant differences in antitumor activity were found. Alternative approaches to intralesional injection were sought. Intradermal injection of BCG adjacent to dermal tumors, prior to surgery, led to eradication of axillary metastases and to the development of tumor-specific transplantation immunity.Successful local BCG immunotherapy is a by-product of the host response to BCG infection. Involved are lymphocytes specifically sensitized to mycobacterial antigens, lymphocyte mediators, and macrophages which develop the capacity to kill tumor cells. Tumor-cell killing may be mediated by exocytosis of macrophage lysosomes into tumor cells. Complete and permanent tumor eradication probably requires the development of tumor-specific transplantation immunity mediated by sensitized lymphocytes. Local infection of the tumor may augment the development of this tumor-specific immunity.
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