Direct measurement of CD8+T cell responses in macaques infected with simian immunodeficiency virus

被引:32
|
作者
Donahoe, SM
Moretto, WJ
Samuel, RV
Metzner, KJ
Marx, PA
Hanke, T
Connor, RI
Nixon, DF
机构
[1] Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10016 USA
[2] John Radcliffe Hosp, Inst Mol Med, MRC, Human Immunol Unit, Oxford OX3 9DS, England
[3] Tulane Univ, Med Ctr, Dept Trop Med, Covington, LA 70433 USA
[4] Tulane Univ, Med Ctr, Tulane Reg Primate Res Ctr, Covington, LA 70433 USA
关键词
D O I
10.1006/viro.2000.0404
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The simian immunodeficiency virus (SIV) macaque model system has been used extensively to study AIDS pathogenesis and to test candidate vaccines for their ability to protect against homologous or heterologous challenge with pathogenic SIV or SHIV. Recent studies suggest that stimulation of HIV-1-specific CTL responses is important for effective vaccination against HIV-1. While quantitative measurements of SIV-specific cytotoxic T lymphocyte (CTL) responses have been facilitated by the use of tetrameric peptide complexes, this technique is currently limited to the study of Mamu-A*01-positive rhesus macaques. Furthermore, very few SIV-specific CTL epitopes have been identified, and there is limited identification of other MHC alleles in macaques. in this study, cytokine flow cytometry (CFC) was used to quantify SIV-specific CD8+ antigen-reactive T cells in macaques infected with SIV. We found a strong correlation (r = 0.96, P < 0.001) between CD8+ antigen-reactive T cells stained with the Mamu-A*01 p11C, C-M tetramer and production of intracellular TNF-or in the CFC assay. Furthermore, the CFC assay was used to identify a novel SIV-specific CTL epitope in Envelope (SIV Env, a.a. 486-494, sequence AEVAELYRL). The use of the CFC assay facilitates the study of antigen-reactive T cell responses in SIV infection and vaccination. (C) 2000 Academic Press.
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收藏
页码:347 / 356
页数:10
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