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人类免疫缺陷病毒特异性CD8(+) T细胞反应无法预测结构化间歇性抗逆转录病毒治疗期间的病毒生长和清除率。

Human immunodeficiency virus-specific CD8(+) T-cell responses do not predict viral growth and clearance rates during structured intermittent antiretroviral therapy.

作者信息

Oxenius Annette, McLean Angela R, Fischer Marek, Price David A, Dawson Sarah J, Hafner Roland, Schneider Christine, Joller Helen, Hirschel Bernard, Phillips Rodney E, Weber Rainer, Günthard Huldrych F

机构信息

Nuffield Department of Clinical Medicine, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, UK.

出版信息

J Virol. 2002 Oct;76(20):10169-76. doi: 10.1128/jvi.76.20.10169-10176.2002.

DOI:10.1128/jvi.76.20.10169-10176.2002
PMID:12239291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC136545/
Abstract

There is a continuing search for better ways to use existing drugs against human immunodeficiency virus (HIV). One idea is to use short therapy interruptions to "autovaccinate" HIV-infected patients. A group of 13 chronically HIV-infected patients enrolled in a trial of such so-called structured treatment interruptions (STIs) were intensively studied with respect to their viral load (VL) and HIV-specific CD8+ T-cell (cytotoxic T-lymphocyte [CTL]) responses. We found that 10 of the 13 patients had plateau VLs after STIs that were lower than their pretreatment VLs. While viral rebound rates became lower over STIs, there were no changes in clearance rates. Although numbers of CTLs did increase over the same time that viral rebounds decreased, there was no correlation between CTL count and either viral rebound rates or clearance rates. Finally, we asked whether absolute numbers of or changes in numbers of CTLs predict plateau VLs after STIs. No measure of CTLs was able to predict plateau VLs. Thus, there was no signature in these data of an important contribution to virological control from HIV-specific CD8+ T lymphocytes.

摘要

人们一直在寻找更好地使用现有抗人类免疫缺陷病毒(HIV)药物的方法。一种想法是利用短期治疗中断来对HIV感染患者进行“自体疫苗接种”。一组13名长期感染HIV的患者参与了一项所谓的结构化治疗中断(STIs)试验,研究人员对他们的病毒载量(VL)和HIV特异性CD8 + T细胞(细胞毒性T淋巴细胞[CTL])反应进行了深入研究。我们发现,13名患者中有10名在STIs后的VL平台期低于其治疗前的VL。虽然在STIs期间病毒反弹率降低,但清除率没有变化。尽管在病毒反弹减少的同一时间内CTL数量确实增加了,但CTL计数与病毒反弹率或清除率之间没有相关性。最后,我们询问CTL的绝对数量或数量变化是否能预测STIs后的VL平台期。没有任何CTL指标能够预测VL平台期。因此,这些数据中没有迹象表明HIV特异性CD8 + T淋巴细胞对病毒学控制有重要贡献。

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2
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3
Structured treatment interruptions for the management of HIV infection.用于管理HIV感染的结构化治疗中断
JAMA. 2001 Dec 19;286(23):2981-7. doi: 10.1001/jama.286.23.2981.
4
HIV viral load response to antiretroviral therapy according to the baseline CD4 cell count and viral load.根据基线CD4细胞计数和病毒载量,HIV病毒载量对抗逆转录病毒疗法的反应。
JAMA. 2001 Nov 28;286(20):2560-7. doi: 10.1001/jama.286.20.2560.
5
Analysis of total human immunodeficiency virus (HIV)-specific CD4(+) and CD8(+) T-cell responses: relationship to viral load in untreated HIV infection.人类免疫缺陷病毒(HIV)特异性CD4(+)和CD8(+) T细胞反应的全面分析:与未经治疗的HIV感染中病毒载量的关系
J Virol. 2001 Dec;75(24):11983-91. doi: 10.1128/JVI.75.24.11983-11991.2001.
6
Structured antiretroviral treatment interruptions in chronically HIV-1-infected subjects.慢性HIV-1感染受试者的结构化抗逆转录病毒治疗中断
Proc Natl Acad Sci U S A. 2001 Nov 6;98(23):13288-93. doi: 10.1073/pnas.221452198. Epub 2001 Oct 30.
7
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8
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9
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10
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