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亚优势CD8 + T细胞反应参与对艾滋病病毒复制的持久控制。

Subdominant CD8+ T-cell responses are involved in durable control of AIDS virus replication.

作者信息

Friedrich Thomas C, Valentine Laura E, Yant Levi J, Rakasz Eva G, Piaskowski Shari M, Furlott Jessica R, Weisgrau Kimberly L, Burwitz Benjamin, May Gemma E, León Enrique J, Soma Taeko, Napoe Gnankang, Capuano Saverio V, Wilson Nancy A, Watkins David I

机构信息

Wisconsin National Primate Research Center, 1220 Capitol Court, Madison, WI 53715-1299, USA.

出版信息

J Virol. 2007 Apr;81(7):3465-76. doi: 10.1128/JVI.02392-06. Epub 2007 Jan 24.

Abstract

"Elite controllers" are individuals that durably control human immunodeficiency virus or simian immunodeficiency virus replication without therapeutic intervention. The study of these rare individuals may facilitate the definition of a successful immune response to immunodeficiency viruses. Here we describe six Indian-origin rhesus macaques that have controlled replication of the pathogenic virus SIVmac239 for 1 to 5 years. To determine which lymphocyte populations were responsible for this control, we transiently depleted the animals' CD8+ cells in vivo. This treatment resulted in 100- to 10,000-fold increases in viremia. When the CD8+ cells returned, control was reestablished and the levels of small subsets of previously subdominant CD8+ T cells expanded up to 2,500-fold above pre-depletion levels. This wave of CD8+ T cells was accompanied by robust Gag-specific CD4 responses. In contrast, CD8+ NK cell frequencies changed no more than threefold. Together, our data suggest that CD8+ T cells targeting a small number of epitopes, along with broad CD4+ T-cell responses, can successfully control the replication of the AIDS virus. It is likely that subdominant CD8+ T-cell populations play a key role in maintaining this control.

摘要

“精英控制者”是指在未经治疗干预的情况下能够持久控制人类免疫缺陷病毒或猴免疫缺陷病毒复制的个体。对这些罕见个体的研究可能有助于明确针对免疫缺陷病毒的成功免疫反应的定义。在此,我们描述了6只印度裔恒河猴,它们已控制致病性病毒SIVmac239的复制达1至5年。为了确定是哪些淋巴细胞群体负责这种控制,我们在体内短暂清除了这些动物的CD8 +细胞。这种处理导致病毒血症增加了100至10000倍。当CD8 +细胞恢复时,病毒复制控制得以重新建立,先前占次要地位的CD8 + T细胞小亚群的水平比清除前水平扩大了2500倍。这一波CD8 + T细胞伴随着强烈的Gag特异性CD4反应。相比之下,CD8 + NK细胞频率变化不超过三倍。总之,我们的数据表明,靶向少数表位的CD8 + T细胞与广泛的CD4 + T细胞反应一起,可以成功控制艾滋病病毒的复制。占次要地位的CD8 + T细胞群体可能在维持这种控制中起关键作用。

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