Université Paris Descartes EA 3620, Sorbonne Paris Cité, Paris.
Clin Infect Dis. 2013 Mar;56(6):880-7. doi: 10.1093/cid/cis999. Epub 2012 Dec 7.
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.
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.
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.
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.
分析了 1128 例原发性人类免疫缺陷病毒 1 型感染(PHI)患者的病毒亚型分布的时间趋势,这些患者的性别、风险组和地理起源分布在法国(1996-2010 年)。研究病毒多样性是否对感染后不久开始联合抗逆转录病毒治疗(cART)的患者的病毒学和免疫学反应产生影响。
研究人群包括在 ANRS-PRIMO 队列中登记的 PHI 患者。通过逆转录酶基因的系统发生分析确定亚型。对那些在 PHI 诊断时开始 cART 的患者评估病毒抑制(<400 拷贝/mL 和 <50 拷贝/mL)和 CD4 T 细胞计数增加情况。
非 B 亚型(285/1128,25.3%)存在于法国所有地区和所有风险组,且随着时间的推移频率增加。非 B 株高度多样化,包括 6 种亚型、10 种循环重组形式(CRF)和几种独特重组形式(URF)。在 cART 的前 2 年内,感染非 B 病毒的患者的病毒学反应与感染 B 病毒的患者相似。感染 CRF02_AG 株或另一种非 B 病毒的患者比感染 B 病毒的患者具有更好的免疫反应。
在过去的 15 年中,法国所有风险组的病毒多样性都有所增加。这是第一项比较自 PHI 以来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)的 cART 具有相似的病毒学和免疫学反应。鉴于 cART 的可用性不断增加,对于非 B 株占主导地位的国家,我们的研究结果令人鼓舞。