Human immunodeficiency virus type-1 (HIV-1)- and Epstein-Barr virus specific cytotoxic T lymphocyte precursors exhibit different kinetics in HIV-1-infected persons

被引:27
作者
Geretti, AM
Dings, MEM
vanEls, CACM
vanBaalen, CA
Wijnholds, FJ
Borleffs, JCC
Osterhaus, ADME
机构
[1] ERASMUS UNIV ROTTERDAM, INST VIROL, 3000 DR ROTTERDAM, NETHERLANDS
[2] NATL INST PUBL HLTH & ENVIRONM PROTECT, LAB VACCINE DEV & IMMUNE MECHANISMS, 3720 BA BILTHOVEN, NETHERLANDS
[3] UNIV UTRECHT HOSP, DEPT IMMUNOL & INTERNAL MED, UTRECHT, NETHERLANDS
关键词
D O I
10.1093/infdis/174.1.34
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 frequencies of human immunodeficiency virus type 1 (HIV-1) Gag- and Epstein-Barr virus (EBV)-specific cytotoxic T lymphocyte precursors (CTLp) were studied longitudinally in peripheral blood mononuclear cells from 9 HIV-1-infected persons. By antigen-specific stimulation, HIV-1 Gag-specific CTLp were detected in vitro throughout the course of HIV-1 infection, even after the onset of overt disease. In 4 patients, however, HIV-I Gag-specific CTLp frequencies declined over time in the presence: of maintained EBV-specific CTLp. This decline was correlated with decreasing CD4 (r = .38; P < .05) and CDS (r = .75; P < .001) cell numbers. The maintenance of EBV-specific CTLp in patients with low CD4 cell numbers indicated that EBV-specific CTL-mediated immunity may remain longer unaffected by HIV-1-induced immune dysfunction. Consistent with this observation, the growth of EBV-specific CTL could be supported in vitro by EBV-infected lymphoblastoid B cell lines, independent of both CD4 cells and exogenous cytokines.
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页码:34 / 45
页数:12
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