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Peripheral CD4 loss of regulatory T cells is associated with persistent viraemia in chronic HIV infection
被引:58
作者:
Baker, C. A. R.
Clark, R.
Ventura, F.
Jones, N. G.
Guzman, D.
Bangsberg, D. R.
Cao, H.
机构:
[1] Calif Dept Hlth Serv, VRDL, Richmond, CA 94804 USA
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
关键词:
HIV;
regulatory T cells;
effector T cells;
viraemia;
D O I:
10.1111/j.1365-2249.2006.03319.x
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Chronic HIV infection is associated with T cell abnormalities and altered effector function. Regulatory T cells (T-reg) are CD4(+) T cells that play a critical role in regulating the immune system. The impact of regulatory T cells on HIV infection and disease progression may be highly significant. We hypothesize that chronic antigenic stimulation from a persistent, high viraemic state may promote a population of T-reg that contributes to HIV-associated immune dysfunction. We evaluated the pattern of T-reg in chronically infected, HIV-positive individuals over a course of 6 months. T-reg are depleted at a distinct rate from that of absolute CD4 cells and loss of T-reg is slower in the presence of viral suppression. In vitro depletion of CD25(+) CD4(+) cells resulted in increased Gag-specific CD4 and CD8 responses. A significant correlation between ex vivo measurement of T-reg and Gag-specific CD4 T cell responses was observed (r = -0.41, P = 0.018) with a trend observed with Gag-specific CD8 T cell responses (P = 0.07). The impact of HIV infection on the T-reg population directly complicates the measured effect of T-reg on the immune dysfunction although our data support the important role of T-reg on modulating the effector T cell response in chronic infection.
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页码:533 / 539
页数:7
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