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人类免疫缺陷病毒(HIV)优先感染HIV特异性CD4 + T细胞。

HIV preferentially infects HIV-specific CD4+ T cells.

作者信息

Douek Daniel C, Brenchley Jason M, Betts Michael R, Ambrozak David R, Hill Brenna J, Okamoto Yukari, Casazza Joseph P, Kuruppu Janaki, Kunstman Kevin, Wolinsky Steven, Grossman Zvi, Dybul Mark, Oxenius Annette, Price David A, Connors Mark, Koup Richard A

机构信息

Vaccine Research Center, NIAID, NIH, Maryland 20892, USA.

出版信息

Nature. 2002 May 2;417(6884):95-8. doi: 10.1038/417095a.

Abstract

HIV infection is associated with the progressive loss of CD4(+) T cells through their destruction or decreased production. A central, yet unresolved issue of HIV disease is the mechanism for this loss, and in particular whether HIV-specific CD4(+) T cells are preferentially affected. Here we show that HIV-specific memory CD4(+) T cells in infected individuals contain more HIV viral DNA than other memory CD4(+) T cells, at all stages of HIV disease. Additionally, following viral rebound during interruption of antiretroviral therapy, the frequency of HIV viral DNA in the HIV-specific pool of memory CD4(+) T cells increases to a greater extent than in memory CD4(+) T cells of other specificities. These findings show that HIV-specific CD4(+) T cells are preferentially infected by HIV in vivo. This provides a potential mechanism to explain the loss of HIV-specific CD4(+) T-cell responses, and consequently the loss of immunological control of HIV replication. Furthermore, the phenomenon of HIV specifically infecting the very cells that respond to it adds a cautionary note to the practice of structured therapy interruption.

摘要

HIV感染与CD4(+) T细胞通过破坏或生成减少而逐步丧失有关。HIV疾病的一个核心但尚未解决的问题是这种丧失的机制,尤其是HIV特异性CD4(+) T细胞是否受到优先影响。在此我们表明,在HIV疾病的所有阶段,感染个体中的HIV特异性记忆CD4(+) T细胞比其他记忆CD4(+) T细胞含有更多的HIV病毒DNA。此外,在抗逆转录病毒治疗中断期间病毒反弹后,HIV特异性记忆CD4(+) T细胞库中HIV病毒DNA的频率比其他特异性记忆CD4(+) T细胞增加的程度更大。这些发现表明,HIV特异性CD4(+) T细胞在体内优先被HIV感染。这提供了一种潜在机制来解释HIV特异性CD4(+) T细胞反应的丧失,进而解释对HIV复制免疫控制的丧失。此外,HIV特异性感染对其产生反应的细胞这一现象给结构化治疗中断的实践敲响了警钟。

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