Abstract
In animal models complete and permanent eradication of tumors can be achieved by adoptive transfer of tumor specific T cells, combined with interleukin 2. The most active cells are CD8+ cytotoxic T lymphocytes (CTL), which recognize peptides of 8-10 amino acids in length, bound to the antigen presenting groove of MHC class I molecules. In the case of virus-induced tumors these peptides are processed from viral proteins. Potentially immunogenic human tumors include melanoma and renal cell carcinoma in addition to the virus-associated cancers Burkitt's lymphoma and cervical carcinoma. The potential of CTL therapy of human cancer needs to be tested with cloned tumor cells. Remedies to over-come poor immunogenicity and evasion by tumor cells of CTL mediated-destruction are discussed.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Amino Acid Sequence
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Animals
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Antigens, Neoplasm / immunology
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HLA Antigens / immunology
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Histocompatibility Antigens Class I / immunology
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Histocompatibility Antigens Class II / immunology
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Humans
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Immune Tolerance
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Immunologic Factors / therapeutic use
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Immunotherapy, Adoptive*
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Interferon-gamma / therapeutic use
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Interleukin-2 / therapeutic use
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Killer Cells, Lymphokine-Activated / immunology
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Lymphocytes, Tumor-Infiltrating / immunology
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Mice
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Molecular Sequence Data
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Neoplasms / immunology
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Neoplasms / prevention & control
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Neoplasms / therapy*
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Neoplasms, Experimental / immunology
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Neoplasms, Experimental / therapy
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Peptide Fragments / immunology
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Peptide Fragments / therapeutic use
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Rats
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T-Lymphocyte Subsets / immunology
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T-Lymphocytes, Cytotoxic / immunology
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T-Lymphocytes, Cytotoxic / transplantation*
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Vaccination
Substances
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Antigens, Neoplasm
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HLA Antigens
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Histocompatibility Antigens Class I
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Histocompatibility Antigens Class II
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Immunologic Factors
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Interleukin-2
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Peptide Fragments
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Interferon-gamma