CTL recognition of HIV-1-infected cells via cross-recognition of multiple overlapping peptides from a single 11-mer Pol sequence

Eur J Immunol. 2012 Oct;42(10):2621-31. doi: 10.1002/eji.201242483. Epub 2012 Aug 6.

Abstract

It is known that overlapping HIV-1 peptides of different lengths can be presented by a given HLA class I molecule. However, the role of those peptides in CD8(+) T cells recognition of HIV-1-infected cells remains unclear. Here we investigated the recognition of overlapping 8-mer to 11-mer peptides of Pol 155-165 by HLA-B*54:01-restricted CD8(+) T cells. The analysis of ex vivo T cells using ELISPOT and tetramer binding assays showed that there were different patterns of CD8(+) T-cell responses to these peptides among chronically HIV-1-infected HLA-B*54:01(+) individuals, though the response to the 9-mer peptide was the strongest among them. CD8(+) T-cell clones with TCRs specific for the 9-mer, 10-mer, and/or 11-mer peptides effectively killed HIV-1-infected cells. Together, these results suggest that the 9-mer and 10-mer peptides could be predominantly presented by HLA-B*54:01, though it remains possible that the 11-mer peptide was also presented by this HLA allele. The present study demonstrates effective CD8(+) T-cell recognition of HIV-1-infected cells via presentation of multiple overlapping HIV-1 peptides and cross-recognition by the CD8(+) T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigen Presentation
  • Clone Cells
  • Cross Reactions
  • Cytotoxicity, Immunologic
  • Enzyme-Linked Immunospot Assay
  • HIV Infections / immunology*
  • HIV-1 / immunology*
  • HLA-B Antigens / immunology
  • Humans
  • Peptide Fragments / genetics
  • Peptide Fragments / immunology*
  • Protein Binding
  • Receptors, Antigen, T-Cell / metabolism
  • T-Lymphocytes, Cytotoxic / immunology*
  • T-Lymphocytes, Cytotoxic / virology
  • pol Gene Products, Human Immunodeficiency Virus / genetics
  • pol Gene Products, Human Immunodeficiency Virus / immunology*

Substances

  • HLA-B Antigens
  • HLA-B54 antigen
  • Peptide Fragments
  • Receptors, Antigen, T-Cell
  • pol Gene Products, Human Immunodeficiency Virus