Interleukin 7 increases human immunodeficiency virus type 1 LAI-mediated Fas-induced T-cell death

被引:22
作者
Lelièvre, JD
Petit, F
Arnoult, D
Ameisen, JC
Estaquier, J
机构
[1] Fac Med Henri Mondor, Lab INSERM, U421, F-94010 Creteil, France
[2] Fac Bichat Claude Bernard, INSERM, EMI, U9922, Paris, France
[3] Inst Pasteur, Unite Physiopathol Infect Lentivirales, Paris, France
关键词
D O I
10.1128/JVI.79.5.3195-3199.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Fas-mediated T-cell death is known to occur during human immunodeficiency virus (HIV) infection. In this study, we found that HIV type 1 LAI (HIV-1(LAI)) primes CD8(+) T cells from healthy donors for apoptosis, which occurs after Fas ligation. This effect is counteracted by a broad caspase inhibitor (zVAD-fmk). Fas-mediated cell death does not depend on CD8(+) T-cell infection, because it occurred in the presence of reverse transcriptase inhibitors. However, purified CD8(+) T cells are sensitive to Fas only in the presence of soluble CD4. Finally, we found that interleukin 7 (IL-7) increases Fas-mediated CD4(+) and CD8(+) T-cell death induced by HIV-1(LAI). Since high levels of IL-7 are a marker of poor prognosis during HIV infection, our data suggest that enhancement of Fas-mediated T-cell death by HIV-1(LAI) and IL-7 is one of the mechanisms involved in progression to AIDS.
引用
收藏
页码:3195 / 3199
页数:5
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