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1型人类免疫缺陷病毒(HIV-1)特异性T细胞反应与猕猴急性HIV-1感染的控制相关。

Human immunodeficiency virus type 1 (HIV-1)-specific T cell responses correlate with control of acute HIV-1 infection in macaques.

作者信息

Kent S J, Woodward A, Zhao A

机构信息

Macfarlane Burnet Centre for Medical Research, Fairfield, Victoria, Australia.

出版信息

J Infect Dis. 1997 Nov;176(5):1188-97. doi: 10.1086/514112.

DOI:10.1086/514112
PMID:9359718
Abstract

Macaca nemestrina efficiently control acute human immunodeficiency virus type 1 (HIV-1) infection. The roles of helper (Th) and cytotoxic (CTL) T cells in controlling acute HIV-1 infection in both peripheral blood and lymph node mononuclear cells (PBMC and LNMC) were assessed in this model. Th and CTL responses to HIV-1 were detected within 2 weeks following HIV-1 infection, and CTL responses to HIV-1 antigens peaked at 4 weeks after infection (>100 HIV-specific CTL/10[6] PBMC), coincident with reductions of HIV-1 RNA and DNA levels in peripheral blood. HIV-1-specific Th and CTL were present in LNMC 6 weeks after infection. Although HIV-1 antibodies were detected 2 weeks after infection, maximal HIV-1 antibody responses were not generated until > 13 weeks after inoculation. Thus, T cell responses temporally correlate with control of HIV-1 in macaques. The induction of a brisk HIV-1-specific CTL response may have been facilitated by a persistent Th response.

摘要

食蟹猴能有效控制急性1型人类免疫缺陷病毒(HIV-1)感染。在该模型中评估了辅助性(Th)和细胞毒性(CTL)T细胞在控制外周血和淋巴结单核细胞(PBMC和LNMC)中急性HIV-1感染的作用。在HIV-1感染后2周内检测到对HIV-1的Th和CTL反应,对HIV-1抗原的CTL反应在感染后4周达到峰值(>100个HIV特异性CTL/10[6]PBMC),这与外周血中HIV-1 RNA和DNA水平的降低同时发生。感染6周后,LNMC中存在HIV-1特异性Th和CTL。虽然感染后2周检测到HIV-1抗体,但直到接种后>13周才产生最大的HIV-1抗体反应。因此,T细胞反应在时间上与猕猴体内HIV-1的控制相关。持续的Th反应可能促进了快速的HIV-1特异性CTL反应的诱导。

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