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减毒的 nef 缺失型 HIV-1 在体内的复制依赖性致病性。

Replication-dependent pathogenicity of attenuated nef-deleted HIV-1 in vivo.

作者信息

Gorry Paul R, Churchill Melissa, Learmont Jennifer, Cherry Catherine, Dyer Wayne B, Wesselingh Steven L, Sullivan John S

机构信息

Macfarlane Burnet Institute for Medical Research and Public Health, Melbourne, Victoria, Australia.

出版信息

J Acquir Immune Defic Syndr. 2007 Dec 1;46(4):390-4. doi: 10.1097/QAI.0b013e31815aba08.

Abstract

BACKGROUND

The Sydney Blood Bank Cohort (SBBC) of long-term survivors consists of 8 individuals infected with an attenuated nef-deleted strain of HIV-1 by means of contaminated blood products donated from a common blood donor between 1981 and 1984. We report the outcome of a 26-year prospective study documenting the clinical course of nef-deleted HIV-1 infection in 7 SBBC members.

METHODS

CD4 T-cell counts and plasma HIV-1 RNA levels were measured by flow cytometry and the COBAS AMPLICOR HIV-1 monitor version 1 or 1.5 (Roche Molecular Diagnostic Systems, Branchburg, NJ), respectively. Changes in these parameters with time were determined by least-squares analysis using STATA (StataCorp, College Station, TX) statistical software.

RESULTS

Four subjects had persistent low-level viremia. Of these, progression to AIDS and/or evidence of CD4 T-cell loss occurred in 3; the fourth viremic individual died of non-HIV-1-related causes in 1995, only 12 years after infection. Three subjects have persistently undetectable plasma HIV-1 RNA levels and remain long-term nonprogressors.

CONCLUSIONS

Our study shows that even weakened highly attenuated HIV-1 strains with nef deletions are ultimately pathogenic in humans unless replication is completely and persistently suppressed in vivo. This finding underscores the importance of aiming to achieve nothing less than complete and sustained suppression of HIV-1 replication by antiretroviral drugs and vaccines.

摘要

背景

悉尼血库长期存活者队列(SBBC)由8名个体组成,他们在1981年至1984年间因接受了来自一名普通献血者的受污染血液制品而感染了一种减毒的、缺失nef基因的HIV-1毒株。我们报告了一项为期26年的前瞻性研究结果,该研究记录了7名SBBC成员中缺失nef基因的HIV-1感染的临床病程。

方法

分别通过流式细胞术和COBAS AMPLICOR HIV-1监测仪版本1或1.5(罗氏分子诊断系统公司,新泽西州布兰奇堡)测量CD4 T细胞计数和血浆HIV-1 RNA水平。使用STATA(StataCorp公司,得克萨斯州大学城)统计软件通过最小二乘法分析确定这些参数随时间的变化。

结果

4名受试者出现持续低水平病毒血症。其中,3人进展为艾滋病和/或出现CD4 T细胞丢失的证据;第四名病毒血症患者于1995年死于非HIV-1相关原因,感染后仅12年。3名受试者的血浆HIV-1 RNA水平持续检测不到,仍然是长期非进展者。

结论

我们的研究表明,即使是缺失nef基因的高度减毒HIV-1毒株,除非在体内完全且持续地抑制其复制,否则最终对人类仍具有致病性。这一发现强调了通过抗逆转录病毒药物和疫苗实现对HIV-1复制的完全且持续抑制的重要性。

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