Pircher Mathilde, Diafouka Merlin, Papuchon Jennifer, Recordon-Pinson Patricia, Mahambou Dominique Nsonde, Akolbout Maryse, Simon Bernard, Fleury Hervé
Laboratoire de Virologie (WHO accredited), CHU de Bordeaux et CNRS UMR 5234 (Microbiologie Fondamentale et Pathogénicité), Université de Bordeaux 2, Bordeaux, France.
AIDS Res Hum Retroviruses. 2012 Dec;28(12):1798-802. doi: 10.1089/aid.2012.0083. Epub 2012 Jul 17.
One hundred patients have been enrolled in the CTA (ambulatory treatment center) of Brazzaville, Republic of Congo, from February to April 2011: 41 naive individuals and 59 patients at failure of first line regimen [two nucleoside reverse transcriptase inhibitors (NRTIs) plus one nonnucleoside reverse transcriptase inhibitor (NNRTI)]. Phylogenetic analysis of HIV-1 isolates allowed identification of subtypes and circulating recombinant forms (CRFs). The drug resistance mutations (DRMs) in reverse transcriptase and protease were analyzed in both subpopulations. Globally, 92 viruses were characterized, exhibiting a high diversity of HIV-1 with a majority of undetermined recombinant forms (URF) followed by CRF02_AG, CRF37_cpx, G, A1, B, D, H, and several other subtypes and CRF: F1, A2, C, CRF13_cpx, CRF11_cpx, CRF20_BG, CRF21_A2D, CRF33_01B G, CRF02_AG, CRF37_cpx, and A1. In naive patients, DRMs were observed with percentages ranging from 4% to 9% depending on drug classes. In treated patients at failure, numerous DRMs could be noted that induce actual or potential resistance to major NRTIs and NNRTIs.
2011年2月至4月,刚果共和国布拉柴维尔的门诊治疗中心(CTA)招募了100名患者:41名初治个体和59名一线治疗方案(两种核苷类逆转录酶抑制剂[NRTIs]加一种非核苷类逆转录酶抑制剂[NNRTIs])失败的患者。对HIV-1分离株进行系统发育分析,以鉴定亚型和循环重组形式(CRFs)。对两个亚组的逆转录酶和蛋白酶中的耐药性突变(DRMs)进行了分析。总体而言,共鉴定了92种病毒,呈现出HIV-1的高度多样性,其中大多数为未确定的重组形式(URF),其次是CRF02_AG、CRF37_cpx、G、A1、B、D、H以及其他几种亚型和CRF:F1、A2、C、CRF13_cpx、CRF11_cpx、CRF20_BG、CRF21_A2D、CRF33_01B G、CRF02_AG、CRF37_cpx和A1。在初治患者中,根据药物类别观察到DRMs的比例在4%至9%之间。在治疗失败的患者中,可发现许多DRMs,这些突变导致对主要NRTIs和NNRTIs产生实际或潜在的耐药性。