Ex vivo T cell-based HIV suppression assay to evaluate HIV-specific CD8+ T-cell responses

被引:68
作者
Saez-Cirion, Asier [1 ]
Shin, So Youn [1 ]
Versmisse, Pierre [1 ]
Barre-Sinoussi, Francoise [1 ]
Pancino, Gianfranco [1 ]
机构
[1] Inst Pasteur, Unite Regulat Infect Retrovirales, Paris, France
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; CONTROLLERS; INFECTION; NONPROGRESSORS; VACCINE; GAG; REPLICATION; ASSOCIATION; LYMPHOCYTES; MECHANISMS;
D O I
10.1038/nprot.2010.73
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To advance T cell-based HIV vaccine development, it is necessary to evaluate the immune correlates of a protective CD8(+) T-cell response. We have developed an assay that assesses the capacity ex vivo of HIV-specific CD8(+) T cells to suppress HIV-1 infection of autologous CD4(+) T cells. this assay directly reflects the ultimate effector function of CD8(+) T cells, the elimination of infected cells, and accurately differentiates the effective CD8(+) T-cell response in spontaneous HIV controllers from ineffective responses in other patients. In this article, we describe all the steps from cell purification to assessment of viral replication by HIV-p24 ELISA and analysis, along with conditions for cell culturing, and how to choose the viral infectious dose that gives the most reliable results. We also depict the conditions of a rapid assay on the basis of flow cytometry analysis of intracellular HIV-Gag products. these procedures take 14-17 d when the p24 ELISA assay is used, or 6 d with the intracellular Gag assay.
引用
收藏
页码:1033 / 1041
页数:9
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