Cytotoxic T lymphocyte therapy of cancer and tumor escape mechanisms

Semin Cancer Biol. 1991 Oct;2(5):347-54.

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

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antigens, Neoplasm / immunology
  • HLA Antigens / immunology
  • Histocompatibility Antigens Class I / immunology
  • Histocompatibility Antigens Class II / immunology
  • Humans
  • Immune Tolerance
  • Immunologic Factors / therapeutic use
  • Immunotherapy, Adoptive*
  • Interferon-gamma / therapeutic use
  • Interleukin-2 / therapeutic use
  • Killer Cells, Lymphokine-Activated / immunology
  • Lymphocytes, Tumor-Infiltrating / immunology
  • Mice
  • Molecular Sequence Data
  • Neoplasms / immunology
  • Neoplasms / prevention & control
  • Neoplasms / therapy*
  • Neoplasms, Experimental / immunology
  • Neoplasms, Experimental / therapy
  • Peptide Fragments / immunology
  • Peptide Fragments / therapeutic use
  • Rats
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocytes, Cytotoxic / immunology
  • T-Lymphocytes, Cytotoxic / transplantation*
  • Vaccination

Substances

  • Antigens, Neoplasm
  • HLA Antigens
  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • Immunologic Factors
  • Interleukin-2
  • Peptide Fragments
  • Interferon-gamma