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Identification and characterization of HIV-1-specific CD8+ T cell epitopes presented by HLA-A*2601.

Abstract
Since HLA-A*26 is one of the most common alleles in Asia, where approximately 20% of people have this allele, identification of HIV-1-specific epitopes presented by HLA-A*26 is necessary for studies on the immunopathogenesis of AIDS and vaccine development in Asia. As presented herein, we used the reverse immunogenetics approach to identify HIV-1 epitopes presented by HLA-A*2601, one of the major HLA-A*26 subtypes. We selected 24 HLA-A*2601-binding peptides out of 110 HIV-1 peptides by using a HLA-A*2601 stabilization assay. The ability of these HLA-A*2601-binding peptides to induce peptide-specific CD8(+) T cells was tested by stimulating PBMCs from HIV-1-infected individuals having HLA-A*2601 with these peptides. Four HLA-A*2601-binding peptides induced peptide-specific CD8 T cells. Analysis using HIV-1 recombinant vaccinia-infected C1R-A*2601 cells indicated that these four peptides were HIV-1 epitopes endogenously presented by HLA-A*2601. Two epitope-specific CD8(+) T cells were predominantly detected in HIV-1 infected individuals, suggesting that these epitopes may be useful for vaccine development.
AuthorsManami Satoh, Yuji Takamiya, Shinichi Oka, Katsushi Tokunaga, Masafumi Takiguchi
JournalVaccine (Vaccine) Vol. 23 Issue 29 Pg. 3783-90 (May 31 2005) ISSN: 0264-410X [Print] Netherlands
PMID15893615 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens, Viral
  • Epitopes, T-Lymphocyte
  • HLA-A Antigens
  • Peptides
  • Interferon-gamma
Topics
  • Animals
  • Antigens, Viral (immunology)
  • CD8-Positive T-Lymphocytes (immunology)
  • Cell Line
  • Cells, Cultured
  • Cytotoxicity Tests, Immunologic
  • Epitopes, T-Lymphocyte (chemistry, immunology)
  • HIV Infections (immunology, virology)
  • HIV-1 (immunology)
  • HLA-A Antigens (immunology)
  • Humans
  • Interferon-gamma (analysis)
  • Mice
  • Peptides (chemical synthesis, chemistry, immunology)
  • Protein Binding

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