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接受非抑制性抗逆转录病毒治疗的C型HIV-1感染个体中的包膜共受体嗜性、耐药性和病毒进化

Envelope coreceptor tropism, drug resistance, and viral evolution among subtype C HIV-1-infected individuals receiving nonsuppressive antiretroviral therapy.

作者信息

Kassaye Seble, Johnston Elizabeth, McColgan Bryan, Kantor Rami, Zijenah Lynn, Katzenstein David

机构信息

Department of Medicine, Division of Infectious Diseases, Stanford University Medical Center, Stanford, CA 94305, USA.

出版信息

J Acquir Immune Defic Syndr. 2009 Jan 1;50(1):9-18. doi: 10.1097/QAI.0b013e31818ffdff.

Abstract

BACKGROUND

In resource-constrained settings, antiretroviral treatment (ART) is often continued based on clinical and CD4 responses, without virologic monitoring. ART with incomplete viral suppression was assessed in 27 subjects with subtype C HIV-1.

METHODS

Plasma HIV-1 RNA, drug resistance, viral tropism, and evolution in polymerase (pol) and envelope (env) genes were measured. The association between these viral parameters and CD4 cell change over time was analyzed using linear regression models.

RESULTS

Increased area under the curve of HIV-1 RNA replication was a predictor of lower CD4 cell gains (P < 0.007), while less drug resistance measured as a genotypic susceptibility score (GSS) (P = 0.065), and lower rates of evolution in pol and env genes (P = 0.08 and 0.097, respectively) measured as genetic distance were modestly associated with increasing CD4 cell counts. Evolution of pol and env were correlated (R2 = 0.48, P = 0.005), however, greater evolution was identified in env vs. pol (P < 0.05). CXCR4-usage (X4) was detected in 14/27 (52%) but no differences in CD4 cell change or plasma viremia were associated with X4-usage.

DISCUSSION

Among subtype C HIV-1 infected patients in Zimbabwe receiving incompletely suppressive ART, higher virus replication and lower CD4 cell gains were associated with drug resistance and evolution of polymerase and envelope.

摘要

背景

在资源有限的环境中,抗逆转录病毒治疗(ART)通常基于临床和CD4反应而持续进行,无需病毒学监测。对27例C型HIV-1感染者接受病毒抑制不完全的ART情况进行了评估。

方法

检测血浆HIV-1 RNA、耐药性、病毒嗜性以及聚合酶(pol)和包膜(env)基因的进化情况。使用线性回归模型分析这些病毒参数与CD4细胞随时间变化之间的关联。

结果

HIV-1 RNA复制曲线下面积增加是CD4细胞增加较少的一个预测指标(P < 0.007),而以基因型易感性评分(GSS)衡量的耐药性较低(P = 0.065),以及以遗传距离衡量的pol和env基因较低的进化率(分别为P = 0.08和0.097)与CD4细胞计数增加适度相关。pol和env的进化具有相关性(R2 = 0.48,P = 0.005),然而,env的进化比pol更显著(P < 0.05)。在14/27(52%)的患者中检测到CXCR4使用型(X4),但X4使用与CD4细胞变化或血浆病毒血症无差异相关。

讨论

在津巴布韦接受病毒抑制不完全的ART的C型HIV-1感染患者中,较高的病毒复制和较低的CD4细胞增加与耐药性以及聚合酶和包膜的进化有关。

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