Loss of CD4+ T cell proliferative ability but not loss of human immunodeficiency virus type 1 specificity equates with progression to disease

被引:103
作者
Wilson, JDK
Imami, N
Watkins, A
Gill, J
Hay, P
Gazzard, B
Westby, M
Gotch, FM
机构
[1] Chelsea & Westminster Hosp, Imperial Coll Sch Med Chelsea & Westminster, Dept Immunol, London SW10 9NH, England
[2] Chelsea & Westminster Hosp, Imperial Coll Sch Med Chelsea & Westminster, Dept HIV Genitourinary Med, London SW10 9NH, England
[3] Roche Discovery, Welwyn Garden City, Herts, England
[4] St George Hosp, Dept Genitourinary Med, Tooting, England
基金
英国惠康基金;
关键词
D O I
10.1086/315764
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this study, we compared human immunodeficiency virus (HIV) type 1-specific proliferative responses with HIV-1-induced intracellular cytokine production in a cohort of clinically nonprogressing patients and individuals with progressive HIV-1 infection. We found strong HIV-1-specific proliferative responses in the clinical nonprogressor cohort that correlated with significant numbers of circulating HIV-1-specific CD4(+) T cells. In contrast, HIV-1-specific proliferative responses were absent in most individuals with progressive HIV-1 infection, even though interferon-gamma-producing HIV-1-specific CD4(+) T cells were detectable by flow cytometry. The implication of these data is that the important dysfunction seen in most HIV-positive patients from very early in disease may be an inability of HIV-1-specific CD4(+) memory T cells to proliferate in response to HIV antigens rather than an absolute loss of circulating virus-specific CD4(+) T cells.
引用
收藏
页码:792 / 798
页数:7
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