Chirwa Lovemore I, Johnson Jeffrey A, Niska Richard W, Segolodi Tebogo M, Henderson Faith L, Rose Charles E, Li Jin-Fen, Thigpen Michael C, Matlhaba Onkabetse, Paxton Lynn A, Brooks John T
aCDC-BOTUSA, Gaborone, Botswana bDivision of HIV/AIDS Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
AIDS. 2014 Jan 14;28(2):223-6. doi: 10.1097/QAD.0000000000000102.
We examined CD4 cell count and plasma viral load patterns among Botswana TDF/FTC Oral HIV Prophylaxis Trial (TDF2 study) participants who seroconverted, comparing participants assigned to receive tenofovir/emtricitabine with participants assigned to receive placebo. We also evaluated for antiretroviral drug resistance among the breakthrough HIV infections. Among nine seroconverters assigned to tenofovir/emtricitabine and 24 to placebo, there were no significant differences in their CD4 cell count or viral load profiles over time. Of the four participants who seroconverted on-study while receiving tenofovir/emtricitabine, none became infected as a result of drug-resistant HIV; moreover, no resistance mutations emerged following seroconversion.
我们对博茨瓦纳替诺福韦/恩曲他滨口服HIV预防试验(TDF2研究)中血清转化的参与者的CD4细胞计数和血浆病毒载量模式进行了检查,将分配接受替诺福韦/恩曲他滨的参与者与分配接受安慰剂的参与者进行比较。我们还评估了突破性HIV感染中的抗逆转录病毒药物耐药性。在分配接受替诺福韦/恩曲他滨的9名血清转化者和分配接受安慰剂的24名血清转化者中,他们的CD4细胞计数或病毒载量随时间变化没有显著差异。在接受替诺福韦/恩曲他滨治疗期间在研究中血清转化的4名参与者中,没有一人因耐药性HIV而感染;此外,血清转化后未出现耐药突变。