Duran Adriana S, Losso Marcelo H, Salomón Horacio, Harris D Robert, Pampuro Sandra, Soto-Ramirez Luis E, Duarte Geraldo, de Souza Ricardo S, Read Jennifer S
Hosp General de Agudos Jose Maria Ramos Mejia, Buenos Aires, Argentina.
AIDS. 2007 Jan 11;21(2):199-205. doi: 10.1097/QAD.0b013e328011770b.
To quantify primary resistance mutations (PRMs) among HIV-1-infected women receiving antiretroviral therapy (ART) for prevention of mother-to-child transmission (MTCT).
Peripheral blood mononuclear cell samples from HIV-1-infected women enrolled in a prospective cohort study in Argentina, the Bahamas, Brazil, and Mexico (NISDI Perinatal Study) were assayed for PRMs. Eligible women were those enrolled by March 2005 and diagnosed with HIV-1 infection during the current pregnancy, and who received ART for MTCT prophylaxis and were followed for 6-12 weeks postpartum.
Of 819 women, 198 met the eligibility criteria. At enrollment, 98% were asymptomatic, 62% had plasma viral load < 1000 copies/ml, 53% had CD4+ cell count > or = 500 cells/microl, and 78% were ART-exposed (mean duration, 8.0 weeks; 95% confidence interval, 7.1-8.9). The most complex ART regimen during pregnancy was usually (81%) a three-drug regimen [two nucleoside reverse transcriptase inhibitors (NRTIs) + one protease inhibitor or two NRTIs + one non-nucleoside reverse transcriptase inhibitor). PRMs were observed in samples from 19 (16%) of 118 women that were amplifiable at one or both time points [11/76 (14%) at enrollment; 14/97 (14%) at 6-12 weeks]. The occurrence of PRMs was not associated with clinical, immunological, or virological disease stage at either time point, whether ART-naive versus exposed at enrollment, or the most complex or number of antiretroviral drug regimens received during pregnancy (P > 0.1). Of 55 women with amplifiable samples at both time points, PRMs were detected in 11 samples (20%).
PRMs occurred among 16.1% of relatively healthy HIV-1-infected mothers from Latin American and Caribbean countries receiving MTCT prophylaxis.
对接受抗逆转录病毒疗法(ART)以预防母婴传播(MTCT)的HIV-1感染女性中的原发性耐药突变(PRM)进行定量分析。
对在阿根廷、巴哈马、巴西和墨西哥开展的一项前瞻性队列研究(NISDI围产期研究)中入组的HIV-1感染女性的外周血单个核细胞样本进行PRM检测。符合条件的女性为2005年3月前入组且在本次妊娠期间被诊断为HIV-1感染,接受ART预防MTCT并在产后随访6至12周的女性。
819名女性中,198名符合入选标准。入组时,98%无症状,62%血浆病毒载量<1000拷贝/毫升,53% CD4 +细胞计数≥500个/微升,78%暴露于ART(平均持续时间8.0周;95%置信区间,7.1 - 8.9)。孕期最复杂的ART方案通常(81%)为三联疗法[两种核苷类逆转录酶抑制剂(NRTI)+一种蛋白酶抑制剂或两种NRTI +一种非核苷类逆转录酶抑制剂]。在118名女性的样本中,有19名(16%)在一个或两个时间点可扩增出PRM [入组时11/76(14%);6至12周时14/97(14%)]。PRM的出现与两个时间点的临床、免疫或病毒学疾病阶段均无关,无论入组时是否初治或暴露于ART,还是孕期接受的最复杂抗逆转录病毒药物方案或数量(P>0.1)。在两个时间点样本均可扩增的55名女性中,11个样本(20%)检测到PRM。
在接受MTCT预防的来自拉丁美洲和加勒比国家的相对健康的HIV-1感染母亲中,16.1%出现了PRM。