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抗逆转录病毒疗法可逆转与HIV相关的淋巴细胞凋亡异常。

Anti-retroviral therapy reverses HIV-associated abnormalities in lymphocyte apoptosis.

作者信息

Johnson N, Parkin J M

机构信息

Department of Immunology, St Bartholomew's and the Royal London School of Medicine and Dentistry, UK.

出版信息

Clin Exp Immunol. 1998 Aug;113(2):229-34. doi: 10.1046/j.1365-2249.1998.00640.x.

DOI:10.1046/j.1365-2249.1998.00640.x
PMID:9717972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1905043/
Abstract

The objective of this study was to assess the role of anti-retroviral therapy (ART) on the susceptibility of peripheral blood lymphocytes (PBL) from HIV-1-infected individuals to activation-induced apoptosis and in comparison with changes in CD4 lymphocyte counts. Eleven symptomatic HIV+ patients were studied. Ex vivo apoptosis was measured in phytohaemagglutinin (PHA)-stimulated PBL and CD4 subsets by flow cytometry, at baseline and after 1 month (4-6 weeks) and 2/3 months of ART. Six patients had extended studies of the effects of therapy to a maximum of 21 months. Lymphocyte apoptosis was significantly elevated in HIV+ patients at baseline (median 22% compared with 7.5% in HIV- risk-matched controls; P < 0.05). This decreased to control levels on ART (7.4% at 4-6 weeks, P < 0.01, and 6.2% at 8-12 weeks, P < 0.05, compared with baseline). Similar changes occurred in the CD4+ subpopulation. The decrease in apoptosis was maintained for several months, but the effect was rapidly lost if ART was discontinued. CD4 counts showed a reciprocal relationship to changes in apoptosis. The association of changes in apoptosis with those in CD4 counts suggests a link between programmed cell death and lymphocyte depletion. Apoptosis reduced in some individuals without any reduction in viral load, suggesting apoptosis may be influenced by factors in addition to the overall extent of HIV replication.

摘要

本研究的目的是评估抗逆转录病毒疗法(ART)对HIV-1感染者外周血淋巴细胞(PBL)激活诱导凋亡易感性的作用,并与CD4淋巴细胞计数的变化进行比较。对11名有症状的HIV+患者进行了研究。通过流式细胞术在基线以及ART治疗1个月(4 - 6周)和2/3个月后,测量植物血凝素(PHA)刺激的PBL和CD4亚群中的体外凋亡情况。6名患者对治疗效果进行了最长达21个月的扩展研究。HIV+患者在基线时淋巴细胞凋亡显著升高(中位数为22%,而HIV风险匹配对照组为7.5%;P < 0.05)。在ART治疗时这一数值降至对照水平(4 - 6周时为7.4%,P < 0.01;8 - 12周时为6.2%,与基线相比P < 0.05)。CD4+亚群也出现了类似变化。凋亡的减少持续了数月,但如果停止ART治疗,这种效果会迅速消失。CD4计数与凋亡变化呈反比关系。凋亡变化与CD4计数变化之间的关联表明程序性细胞死亡与淋巴细胞耗竭之间存在联系。在一些个体中凋亡减少,但病毒载量没有任何降低,这表明凋亡可能受到除HIV复制总体程度之外的因素影响。

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