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.
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Authors | Manami Satoh, Yuji Takamiya, Shinichi Oka, Katsushi Tokunaga, Masafumi Takiguchi |
Journal | Vaccine
(Vaccine)
Vol. 23
Issue 29
Pg. 3783-90
(May 31 2005)
ISSN: 0264-410X [Print] Netherlands |
PMID | 15893615
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antigens, Viral
- Epitopes, T-Lymphocyte
- HLA-A Antigens
- Peptides
- Interferon-gamma
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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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