Identification of a shared epitope recognized by melanoma-specific, HLA-A3-restricted cytotoxic T lymphocytes

Immunol Lett. 2003 Dec 15;90(2-3):131-5. doi: 10.1016/j.imlet.2003.08.003.

Abstract

We previously established a melanoma-reactive cytotoxic T lymphocyte (CTL) line that recognizes multiple epitopes in the context of HLA-A3. To increase the number of peptides available for use in a vaccine for the treatment of melanoma, we identified one of these epitopes, SQNFPGSQK, through a combination of epitope reconstitution experiments and mass spectrometry. The SQNFPGSQK peptide was also found to be associated with HLA-A3 on an additional melanoma tumor line, thus indicating that the peptide is not unique to the melanoma tumor line from which it was isolated and thus, unlikely to arise through a mutational event. Although the protein origin of SQNFPGSQK has yet to be established, the shared nature of this epitope and the fact that it elicits a natural immune response indicates that it warrants further study to determine its usefulness as a vaccine component for the treatment of melanoma. The peptide may also be useful as a research tool for evaluating spontaneous anti-tumor immune responses in patients with melanoma.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Cell Line, Tumor
  • Chromatography, High Pressure Liquid
  • Chromium Radioisotopes
  • Epitopes, T-Lymphocyte / chemistry
  • Epitopes, T-Lymphocyte / genetics
  • Epitopes, T-Lymphocyte / immunology*
  • HLA-A3 Antigen / immunology*
  • Humans
  • Mass Spectrometry
  • Melanoma / immunology*
  • Peptides / chemistry
  • Peptides / genetics
  • Peptides / immunology
  • Sequence Homology
  • T-Lymphocytes, Cytotoxic / immunology*

Substances

  • Chromium Radioisotopes
  • Epitopes, T-Lymphocyte
  • HLA-A3 Antigen
  • Peptides