Taylor Barbara S, Hunt Gillian, Abrams Elaine J, Coovadia Ashraf, Meyers Tammy, Sherman Gayle, Strehlau Renate, Morris Lynn, Kuhn Louise
Division of Infectious Diseases, Department of Medicine, University of Texas Health Sciences Center at San Antonio, USA.
AIDS Res Hum Retroviruses. 2011 Sep;27(9):945-56. doi: 10.1089/aid.2010.0205. Epub 2011 Mar 23.
Data on the development of antiretroviral drug resistance in HIV-1-infected children receiving protease inhibitor (PI)-based antiretroviral therapy (ART) are limited. We examined antiretroviral resistance among a cohort of 323 South African HIV-infected children <2 years old exposed to nevirapine for prevention of mother-to-child transmission. Ritonavir (RTV) was used initially for 138 children who were <6 months old or receiving antimycobacterial therapy; otherwise children received lopinavir/ritonavir (LPV/r)-based ART. HIV-1 population sequencing of the pol gene was conducted on all pretreatment samples and on posttreatment samples for children who did not achieve HIV-1 plasma RNA <400 copies/ml by 52 weeks. Among children in the cohort, 38 died, 22 had <24 weeks follow-up, 209 achieved virologic suppression, and 54 did not. Of 41 children without virologic suppression with posttreatment HIV genotype data available, major resistance mutations were found in 32 (78%): 14 (36%) had PI mutations including V82A, M46I, and L90M; 29 (71%) had M184V/I; and three had NNRTI mutations (K103N, Y181C, and G190A). Among the children who did not achieve virologic suppression, none of the seven children treated exclusively with LPV/r developed PI-related mutations, compared with 14 of 32 (44%) who received RTV-based regimens (p=0.036); PI genotypes were unavailable for two children. Seventy-eight percent of children without virologic suppression developed resistance mutations that impact second-line ART options. Only children who received RTV-based ART developed major PI-related resistance mutations, and use of this regimen should be avoided.
关于接受基于蛋白酶抑制剂(PI)的抗逆转录病毒疗法(ART)的HIV-1感染儿童中抗逆转录病毒药物耐药性发展的数据有限。我们调查了323名南非2岁以下接受奈韦拉平预防母婴传播的HIV感染儿童队列中的抗逆转录病毒耐药性情况。最初,138名6个月以下或正在接受抗分枝杆菌治疗的儿童使用了利托那韦(RTV);否则,儿童接受基于洛匹那韦/利托那韦(LPV/r)的ART。对所有治疗前样本以及52周时未实现HIV-1血浆RNA<400拷贝/ml的儿童的治疗后样本进行了pol基因的HIV-1群体测序。在该队列儿童中,38人死亡,22人随访时间不足24周,209人实现了病毒学抑制,54人未实现。在41名有治疗后HIV基因型数据且未实现病毒学抑制的儿童中,32人(78%)发现了主要耐药突变:14人(36%)有PI突变,包括V82A、M46I和L90M;29人(71%)有M184V/I;3人有非核苷类逆转录酶抑制剂(NNRTI)突变(K103N、Y181C和G190A)。在未实现病毒学抑制的儿童中,仅接受LPV/r治疗的7名儿童均未发生PI相关突变,而接受基于RTV方案治疗的32名儿童中有14人(44%)发生了此类突变(p=0.036);有两名儿童的PI基因型数据不可用。未实现病毒学抑制的儿童中有78%发生了影响二线ART选择的耐药突变。仅接受基于RTV的ART的儿童发生了主要的PI相关耐药突变,应避免使用该方案。