Identification of a conserved universal Th epitope in HIV-1 reverse transcriptase that is processed and presented to HIV-specific CD4+ T cells by at least four unrelated HLA-DR molecules

J Immunol. 1999 Jan 1;162(1):152-60.

Abstract

CD4+ Th cells play an important role in the induction and maintenance of specific T cell immunity. Indications for a protective role of CD4+ T cells against HIV-1 infection were found in subjects who were able to control HIV-1 viremia as well as in highly HIV-1-exposed, yet seronegative, individuals. This study describes the identification of an HIV-1-specific Th epitope that exhibits high affinity binding as well as high immunogenicity in the context of at least four different HLA-DR molecules that together cover 50-60% of the Caucasian, Oriental, and Negroid populations. This HIV-1 reverse transcriptase-derived peptide (RT171-190) is highly conserved among different HIV-1 isolates. Importantly, stimulation of PBL cultures from HIV-1 seronegative donors with this peptide resulted in Thl-type lymphocytes capable of efficient recognition of HIV-1-pulsed APCs. Taken together, these data indicate that peptide RT171-190 constitutes an attractive component of vaccines aiming at induction or enhancement of HIV-1-specific T cell immunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Antigen Presentation*
  • CD4-Positive T-Lymphocytes / enzymology
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / virology
  • Clone Cells
  • Conserved Sequence*
  • Cytokines / biosynthesis
  • Epitopes, T-Lymphocyte / chemistry
  • Epitopes, T-Lymphocyte / immunology
  • Epitopes, T-Lymphocyte / metabolism*
  • HIV Reverse Transcriptase / immunology*
  • HIV Reverse Transcriptase / metabolism
  • HIV-1 / immunology*
  • HLA-DR Antigens / metabolism*
  • Humans
  • Lymphocyte Activation / drug effects
  • Molecular Sequence Data
  • Peptides / immunology
  • Peptides / metabolism
  • Peptides / pharmacology
  • Protein Binding / immunology
  • T-Lymphocyte Subsets / enzymology
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / virology
  • T-Lymphocytes, Helper-Inducer / enzymology
  • T-Lymphocytes, Helper-Inducer / immunology*
  • T-Lymphocytes, Helper-Inducer / virology

Substances

  • Cytokines
  • Epitopes, T-Lymphocyte
  • HLA-DR Antigens
  • Peptides
  • HIV Reverse Transcriptase