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体内CD8 +淋巴细胞的猿猴免疫缺陷病毒感染

Simian immunodeficiency virus infection of CD8+ lymphocytes in vivo.

作者信息

Dean G A, Reubel G H, Pedersen N C

机构信息

Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis 95616, USA.

出版信息

J Virol. 1996 Aug;70(8):5646-50. doi: 10.1128/JVI.70.8.5646-5650.1996.

Abstract

To determine the lymphoid target cells of simian immunodeficiency virus (SIV) in vivo, peripheral blood lymphocytes (PBL) and lymph node lymphocytes (LNL) were positively selected (>97% purity) for surface expression of CD4, CD8, or CD20 and then analyzed for SIV provirus using semiquantitative DNA amplification. We found provirus in CD4+ and CD8+ lymphocytes but none in CD20+ lymphocytes. During acute SIV infection (< or = 214 days postinoculation), the percentage of PBL and LNL CD4+ cells containing proviral DNA ranged from 0.2 to 20% and from 0.2 to 2%, respectively. Proviral burden in the CD8+ population of either PBL or LNL ranged from 0.01 to 0.2%. Virus isolation by cocultivation was positive for both CD4+ and CD8+ purified populations. No difference in proviral burden was observed between PBL and LNL subsets during acute SIV infection. Up to 19.4% of positively selected CD8+ cells also expressed CD4, and thus the provirus may reside within a dual-positive population. This dual-positive population may represent activated lymphocytes that are particularly susceptible to infection and may provide an opportunity for virus entry into the CD8+ CD4- lymphocytes in vivo.

摘要

为了在体内确定猿猴免疫缺陷病毒(SIV)的淋巴靶细胞,对外周血淋巴细胞(PBL)和淋巴结淋巴细胞(LNL)进行表面CD4、CD8或CD20表达的阳性选择(纯度>97%),然后使用半定量DNA扩增分析SIV前病毒。我们在CD4+和CD8+淋巴细胞中发现了前病毒,但在CD20+淋巴细胞中未发现。在急性SIV感染期间(接种后≤214天),含有前病毒DNA的PBL和LNL CD4+细胞的百分比分别为0.2%至20%和0.2%至2%。PBL或LNL的CD8+群体中的前病毒载量范围为0.01%至0.2%。通过共培养进行病毒分离,CD4+和CD8+纯化群体均呈阳性。在急性SIV感染期间,PBL和LNL亚群之间未观察到前病毒载量的差异。高达19.4%的阳性选择的CD8+细胞也表达CD4,因此前病毒可能存在于双阳性群体中。这个双阳性群体可能代表特别容易感染的活化淋巴细胞,并可能为病毒在体内进入CD8+ CD4-淋巴细胞提供机会。

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