Superior control of HIV-1 replication by CD8+ T cells is reflected by their avidity, polyfunctionality, and clonal turnover

被引:578
作者
Almeida, Jorge R.
Price, David A.
Papagno, Laura
Arkoub, Zaina Ait
Sauce, Delphine
Bornstein, Ethan
Asher, Tedi E.
Samri, Assia
Schnuriger, Aurelie
Theodorou, Ioannis
Costagliola, Dominique
Rouzioux, Christine
Agut, Henri
Marcelin, Anne-Genevieve
Douek, Daniel
Autran, Brigitte
Appay, Victor [1 ]
机构
[1] INSERM, Cellular Immunol Lab, U543, Avenir Grp, F-75654 Paris 13, France
[2] Univ Paris 06, Hop La Pitie Salpetriere, Virol Lab, UPRES EA2387, F-75013 Paris, France
[3] Univ Paris 06, Hop La Pitie Salpetriere, U720, INSERM, F-75013 Paris, France
[4] NIH, Human Immunol Sect, Vaccine Res Ctr, Bethesda, MD 20892 USA
[5] Univ Oxford, John Radcliffe Hosp, Weatherall Inst Mol Med, Oxford OX3 9DS, England
[6] Univ Rene Descartes Paris 5, Virol Lab, Hop Necker Enfants Malad, F-75015 Paris, France
基金
英国医学研究理事会;
关键词
D O I
10.1084/jem.20070784
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The key attributes of CD8(+) T cell protective immunity in human immunodeficiency virus ( HIV) infection remain unclear. We report that CD8(+) T cell responses specific for Gag and, in particular, the immunodominant p24 epitope KK10 correlate with control of HIV- 1 replication in human histocompatibility leukocyte antigen ( HLA) - B27 patients. To understand further the nature of CD8(+) T cell - mediated antiviral efficacy, we performed a comprehensive study of CD8(+) T cells specific for the HLA- B27 - restricted epitope KK10 in chronic HIV- 1 infection based on the use of multiparametric flow cytometry together with molecular clonotypic analysis and viral sequencing. We show that B27- KK10 - specific CD8(+) T cells are characterized by polyfunctional capabilities, increased clonal turnover, and superior functional avidity. Such attributes are interlinked and constitute the basis for effective control of HIV- 1 replication. These data on the features of effective CD8(+) T cells in HIV infection may aid in the development of successful T cell vaccines.
引用
收藏
页码:2473 / 2485
页数:13
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