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首页> 外文期刊>Clinical infectious diseases >Increasing HIV-1 non-B subtype primary infections in patients in France and effect of HIV subtypes on virological and immunological responses to combined antiretroviral therapy
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Increasing HIV-1 non-B subtype primary infections in patients in France and effect of HIV subtypes on virological and immunological responses to combined antiretroviral therapy

机译:法国患者中HIV-1非B亚型原发感染的增加以及HIV亚型对联合抗逆转录病毒疗法的病毒学和免疫学反应的影响

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Background. To analyze the time trends of the viral subtype distributions according to gender, risk group, and geographical origin of the patients in 1128 primary human immunodeficiency virus type 1 infection (PHI), diagnosed in France (1996-2010). To study whether the viral diversity had an impact on the virological and immunological responses in patients initiating combined antiretroviral therapy (cART) soon after infection. Methods. The study population comprised PHI patients enrolled in the ANRS-PRIMO-cohort. Subtypes were determined by phylogenetic analysis of reverse transcriptase gene. Viral suppression (<400 copies/mL and <50 copies/mL) and CD4 T-cell counts increase were assessed for those who initiated cART at PHI diagnosis. Results. Non-B subtypes (285/1128, 25.3%) were present in all regions of France and all risk groups, and increased in frequency over time. Non-B strains were highly diverse and included 6 subtypes, 10 circulating recombinant forms (CRFs), and several unique recombinant forms (URFs). Virological response in patients infected with a non-B virus was similar to that of patients with a subtype-B virus over the first 2 years of cART. Patients infected with either a CRF02-AG strain or another non-B virus had better immunological responses than those infected with a subtype-B virus. Conclusions. Over the last 15 years in France, viral diversity has increased in all risk groups. This is the first large study comparing the responses of patients treated since PHI and showing a similar virological and immunological response to cART between the 2 groups of patients (B and non-B). Our results are encouraging for countries where non-B strains predominate in view of the increasing availability of cART. ? 2012 The Author 2012. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved.
机译:背景。目的分析法国(1996-2010年)诊断的1128例原发性人类免疫缺陷病毒1型感染(PHI)中患者的性别,风险组和地理来源的病毒亚型分布的时间趋势。研究在感染后立即开始联合抗逆转录病毒治疗(cART)的患者中病毒多样性是否对病毒学和免疫学反应有影响。方法。研究人群包括ANRS-PRIMO队列中的PHI患者。通过系统发育分析逆转录酶基因确定亚型。对在PHI诊断时启动cART的患者进行了病毒抑制(<400拷贝/ mL和<50拷贝/ mL)和CD4 T细胞计数增加的评估。结果。在法国所有地区和所有危险人群中均存在非B型亚型(285/1128,占25.3%),并且其频率随时间增加。非B株非常多样,包括6个亚型,10个循环重组体(CRF)和几种独特的重组体(URF)。在cART的最初两年中,非B病毒感染患者的病毒学应答与B亚型病毒患者的病毒学应答相似。感染CRF02-AG菌株或另一种非B病毒的患者的免疫反应比感染B亚型病毒的患者更好。结论在法国的过去15年中,所有风险组的病毒多样性都在增加。这是第一项比较PHI后接受治疗的患者反应的大型研究,结果显示两组患者(B和非B)对cART的病毒学和免疫学反应相似。鉴于cART的可用性越来越高,对于非B株占主导地位的国家,我们的结果令人鼓舞。 ? 2012作者2012。由牛津大学出版社代表美国传染病学会出版。版权所有。

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