Peptide-MHC multimer-based monitoring of CD8 T-cells in HIV-1 infection and AIDS vaccine development

Expert Rev Vaccines. 2015 Jan;14(1):69-84. doi: 10.1586/14760584.2015.962520. Epub 2014 Nov 5.

Abstract

The use of MHC multimers allows precise and direct detecting and analyzing of antigen-specific T-cell populations and provides new opportunities to characterize T-cell responses in humans and animals. MHC-multimers enable us to enumerate specific T-cells targeting to viral, tumor and vaccine antigens with exceptional sensitivity and specificity. In the field of HIV/SIV immunology, this technique provides valuable information about the frequencies of HIV- and SIV-specific CD8(+) cytotoxic T lymphocytes (CTLs) in different tissues and sites of infection, AIDS progression, and pathogenesis. Peptide-MHC multimer technology remains a very sensitive tool in detecting virus-specific T -cells for evaluation of the immunogenicity of vaccines against HIV-1 in preclinical trials. Moreover, it helps to understand how immune responses are formed following vaccination in the dynamics from priming point until T-cell memory is matured. Here we review a diversity of peptide-MHC class I multimer applications for fundamental immunological studies in different aspects of HIV/SIV infection and vaccine development.

Keywords: AIDS; CD4+ T-cells; CD8+ CTL; CD8+ T-cells; HIV-1; MHC class I molecules; SIV; TCR; affinity; avidity; cytokines; peptide-MHC multimer; peptide-MHC tetramer; vaccine.

Publication types

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

MeSH terms

  • AIDS Vaccines / immunology*
  • Antigens, Viral / immunology
  • CD8-Positive T-Lymphocytes / immunology*
  • Cytological Techniques / methods*
  • Fluorometry
  • HIV Infections / immunology*
  • HIV-1 / immunology*
  • Histocompatibility Antigens Class I / immunology
  • Humans
  • Immunologic Techniques / methods*
  • Recombinant Proteins / immunology
  • Staining and Labeling / methods*

Substances

  • AIDS Vaccines
  • Antigens, Viral
  • Histocompatibility Antigens Class I
  • Recombinant Proteins