A mutated HLA-A2 molecule recognized by autologous cytotoxic T lymphocytes on a human renal cell carcinoma

J Exp Med. 1996 Jun 1;183(6):2501-8. doi: 10.1084/jem.183.6.2501.

Abstract

Many human tumor cells have been shown to express antigens that are recognized by autologous cytotoxic T lymphocytes (CTL) and the molecular nature of a number of melanoma antigens has been defined recently. Here we describe the characterization of an antigen recognized on a renal cell carcinoma by autologous CTL clones. This antigen is encoded by the HLA-A2 gene present in the tumor cells. The sequence of this gene differs from the HLA-A2 sequence found in autologous peripheral blood lymphocytes by a point mutation that results in an arginine to isoleucine exchange at residue 170, which is located on the alpha-helix of the alpha 2 domain. Transfection experiments with the normal and mutated HLA-A2 cDNA demonstrated that this amino acid replacement was responsible for the recognition of the HLA-A2 molecule expressed on the tumor cells. The mutant HLA-A2 gene was also detected in the original tumor tissue from the patient, excluding the possibility that the mutation had appeared in vitro. Thus, HLA class I molecules carrying a tumor-specific mutation can be involved in the recognition of tumor cells by autologous CTL.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Carcinoma, Renal Cell / genetics
  • Carcinoma, Renal Cell / immunology*
  • Cell Line
  • Chlorocebus aethiops
  • Cytotoxicity, Immunologic*
  • DNA Primers
  • Gene Library
  • Genes, MHC Class I*
  • HLA-A2 Antigen / chemistry
  • HLA-A2 Antigen / genetics*
  • HLA-A2 Antigen / immunology
  • Humans
  • Kidney Neoplasms / genetics
  • Kidney Neoplasms / immunology*
  • Models, Structural
  • Molecular Sequence Data
  • Point Mutation*
  • Polymerase Chain Reaction
  • Protein Structure, Secondary
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / immunology
  • T-Lymphocytes, Cytotoxic / immunology*
  • Transfection
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • DNA Primers
  • HLA-A2 Antigen
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha