Identification of new epitopes from four different tumor-associated antigens: recognition of naturally processed epitopes correlates with HLA-A*0201-binding affinity

J Immunol. 2001 Jul 15;167(2):787-96. doi: 10.4049/jimmunol.167.2.787.

Abstract

Forty-two wild-type and analogue peptides derived from p53, carcinoembryonic Ag, Her2/neu, and MAGE2/3 were screened for their capacity to induce CTLs, in vitro, capable of recognizing tumor target lines. All the peptides bound HLA-A*0201 and two or more additional A2 supertype alleles with an IC(50) of 500 nM or less. A total of 20 of 22 wild-type and 9 of 12 single amino acid substitution analogues were found to be immunogenic in primary in vitro CTL induction assays, using normal PBMCs and GM-CSF/IL-4-induced dendritic cells. These results suggest that peripheral T cell tolerance does not prevent, in this system, induction of CTL responses against tumor-associated Ag peptides, and confirm that an HLA class I affinity of 500 nM or less is associated with CTL epitope immunogenicity. CTLs generated by 13 of 20 of the wild-type epitopes, 6 of 9 of the single, and 2 of 5 of the double substitution analogues tested recognized epitopes generated by endogenous processing of tumor-associated Ags and expressed by HLA-matched cancer cell lines. Further analysis revealed that recognition of naturally processed Ag was correlated with high HLA-A2.1-binding affinity (IC(50) = 200 nM or less; p = 0.008), suggesting that high binding affinity epitopes are frequently generated and can be recognized as a result of natural Ag processing. These results have implications for the development of cancer vaccines, in particular, and for the process of epitope selection in general.

Publication types

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

MeSH terms

  • Alleles
  • Amino Acid Substitution / immunology
  • Antigen Presentation*
  • Antigens, Neoplasm / immunology
  • Antigens, Neoplasm / metabolism*
  • Carcinoembryonic Antigen / immunology
  • Carcinoembryonic Antigen / metabolism
  • Cell Line, Transformed
  • Cells, Cultured
  • Cytotoxicity Tests, Immunologic
  • Epitopes, T-Lymphocyte / immunology
  • Epitopes, T-Lymphocyte / metabolism*
  • Female
  • HLA-A2 Antigen / immunology
  • HLA-A2 Antigen / metabolism*
  • Humans
  • Lymphocyte Activation
  • Male
  • Neoplasm Proteins / immunology
  • Neoplasm Proteins / metabolism
  • Peptide Fragments / immunology
  • Peptide Fragments / metabolism
  • Protein Binding / genetics
  • Protein Binding / immunology
  • Receptor, ErbB-2 / immunology
  • Receptor, ErbB-2 / metabolism
  • T-Lymphocytes, Cytotoxic / immunology
  • T-Lymphocytes, Cytotoxic / metabolism
  • Tumor Cells, Cultured
  • Tumor Suppressor Protein p53 / immunology
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Antigens, Neoplasm
  • Carcinoembryonic Antigen
  • Epitopes, T-Lymphocyte
  • HLA-A2 Antigen
  • MAGEA3 protein, human
  • MAGEB2 protein, human
  • Neoplasm Proteins
  • Peptide Fragments
  • Tumor Suppressor Protein p53
  • Receptor, ErbB-2