Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Department of Pediatrics, Surin Hospital, Surin, Thailand.
J Pediatric Infect Dis Soc. 2021 Feb 13;10(1):1-6. doi: 10.1093/jpids/piaa004.
Maraviroc, a C-C chemokine receptor 5 (CCR5) antagonist, has been used as an alternative antiretroviral drug in treatment-experienced adults and children infected by CCR5-tropic human immunodeficiency virus type 1 (HIV-1) isolates. Prior to widespread use of this drug, rates of HIV-1 coreceptor tropism and factors associated with coreceptor tropism had to be determined.
HIV-1-infected individuals aged <20 years with HIV-1 viral loads >1000 RNA copies/mL who were treatment-experienced or treatment-naive were enrolled. HIV-1 coreceptor tropism was determined using a genotypic test in which V3 sequences were analyzed with GENO2PHENO version 2.5 and a false discovery rate of 5%.
Fifty-two HIV-1-infected patients were recruited. The median age of participants was 14.9 years (interquartile range [IQR], 8.9-16.8 years). The median CD4 cell count was 396.0 cells/µL (IQR, 72.0-630.3 cells/µL). The median HIV-1 viral load was 43 339 RNA copies/mL (IQR, 8874-197 055 copies/mL). Thirty-nine patients (75%) were treatment-experienced. The most prevalent HIV-1 subtype in this population was CRF01_AE (36 patients, 69.2%). Based on analyses of V3 loop sequences, 5 of 13 treatment-naive patients (38.5%) and 11 of 39 treatment-experienced patients (28.2%) were infected by R5 viruses, while 7 of 13 treatment-naive patients (53.8%) and 19 of 39 treatment-experienced patients (48.7%) were infected by X4 viruses. The only factor associated with the presence of X4 viruses was HIV-1 subtype CRF01_AE.
X4-tropic viruses are associated with the CRF01_AE subtype. Hence, testing of HIV tropism should be performed before treatment with CCR5 inhibitors in children in areas where CRF01_AE predominates.
马拉维若(Maraviroc)是一种 C-C 趋化因子受体 5(CCR5)拮抗剂,已被用作治疗经验丰富的成人和儿童感染 CCR5 嗜性人类免疫缺陷病毒 1(HIV-1)分离株的替代抗逆转录病毒药物。在广泛使用这种药物之前,必须确定 HIV-1 核心受体嗜性以及与核心受体嗜性相关的因素。
我们招募了年龄<20 岁且 HIV-1 病毒载量>1000 RNA 拷贝/mL 的、有治疗经验或无治疗经验的 HIV-1 感染者。使用 GENO2PHENO 版本 2.5 分析 V3 序列,并采用错误发现率为 5%的基因测试来确定 HIV-1 核心受体嗜性。
共纳入 52 名 HIV-1 感染者。参与者的中位年龄为 14.9 岁(四分位距[IQR],8.9-16.8 岁)。中位 CD4 细胞计数为 396.0 个/µL(IQR,72.0-630.3 个/µL)。中位 HIV-1 病毒载量为 43339 RNA 拷贝/mL(IQR,8874-197055 拷贝/mL)。39 名患者(75%)有治疗经验。该人群中最常见的 HIV-1 亚型为 CRF01_AE(36 名患者,69.2%)。基于 V3 环序列分析,13 名无治疗经验的患者中有 5 名(38.5%)和 39 名有治疗经验的患者中有 11 名(28.2%)感染了 R5 病毒,而 13 名无治疗经验的患者中有 7 名(53.8%)和 39 名有治疗经验的患者中有 19 名(48.7%)感染了 X4 病毒。唯一与 X4 病毒存在相关的因素是 HIV-1 亚型 CRF01_AE。
X4 嗜性病毒与 CRF01_AE 亚型相关。因此,在以 CRF01_AE 为主的地区,在使用 CCR5 抑制剂治疗之前,应检测 HIV 嗜性。