Characterization of virus-specific CD8+ effector T cells in the course of HIV-1 infection:: longitudinal analyses in slow and rapid progressors

被引:22
作者
Jansen, CA
Piriou, E
Bronke, C
Vingerhoed, J
Kostense, S
van Baarle, D
Miedema, F
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Clin Viroimmunol, Sanquin Res, NL-1066 CX Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Landsteiner Lab, NL-1066 CX Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Human Retrovirol, NL-1105 AZ Amsterdam, Netherlands
关键词
HIV; EBV; CMV; CTL; cellular differentiation; AIDS;
D O I
10.1016/j.clim.2004.08.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Studies in humans have provided evidence that CD8(+) T cells exhibit distinct phenotypical and functional properties dependent on virus specificity. It is not known how these T-cell phenotypes develop over the course of infection. Dynamics and properties of T cells specific for human immunodeficiency virus (HIV), cytomegalovirus (CMV), and Epstein-Barr virus (EBV) in HIV infection were investigated in relation to viral load. In rapid progressors, HIV-specific CD8(+) T cells were less differentiated early in infection and did not develop a more differentiated phenotype. In slow progressors, perforin expression of HIV-specific CD8(+) T cells slightly increased over time. HIV and EBV loads were detectable in all individuals, while CMV load could not be detected. Thus, in individuals with progressive HIV infection, HIV-specific T cells are less differentiated already early in infection. This apparent block in differentiation may be partly caused by chronic viremia or lack of CD4(+) T-cell help. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:299 / 309
页数:11
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