Ruone Susan, Paxton Lynn, McLaurin Tony, Taylor Allan, Hanson Debra, Heneine Walid, Brooks John T, García-Lerma José Gerardo
*Laboratory Branch, Division of HIV/AIDS Prevention, National Center for HIV, Hepatitis, STD, and Prevention, Centers for Disease Control and Prevention, Atlanta, GA; and †Epidemiology Branch, Division of HIV/AIDS Prevention, National Center for HIV, Hepatitis, STD, and Prevention, Centers for Disease Control and Prevention, Atlanta, GA.
J Acquir Immune Defic Syndr. 2016 Jun 1;72(2):129-32. doi: 10.1097/QAI.0000000000000921.
We describe HIV-1 evolutionary dynamics in the 4 participants from the TDF2-PrEP trial who became HIV-1 infected while prescribed emtricitabine and tenofovir disoproxil fumarate (FTC/TDF). At seroconversion, virus diversity in the 2 participants with detectable drug was only 0.05% (95% confidence intervals: 0.04 to 0.06) and 0.07% (0.06 to 0.08) compared with 2.25% (1.95 to 2.6) and 0.42% (0.36 to 0.49) in those with no detectable drug and 0.07%-0.69% in 5 placebo recipients (P > 0.5). At 10 months, diversity in adherent participants was only 0.37% (0.31 to 0.41) and 0.86% (0.82 to 0.90) compared with 0.5%-1.7% among participants who did not take FTC/TDF (P > 0.5). Although limited by the small number of infections that reduced the power to detect differences, we found that sequences from seroconverters with detectable drug were more homogeneous than those from placebo or nonadherent seroconverters.
我们描述了来自TDF2-PrEP试验的4名参与者感染HIV-1的进化动态,这些参与者在服用恩曲他滨和替诺福韦酯富马酸盐(FTC/TDF)时感染了HIV-1。在血清转化时,2名可检测到药物的参与者的病毒多样性仅为0.05%(95%置信区间:0.04至0.06)和0.07%(0.06至0.08),而未检测到药物的参与者为2.25%(1.95至2.6)和0.42%(0.36至0.49),5名安慰剂接受者为0.07%-0.69%(P>0.5)。在10个月时,坚持服药的参与者的多样性仅为0.37%(0.31至0.41)和0.86%(0.82至0.90),而未服用FTC/TDF的参与者为0.5%-1.7%(P>0.5)。尽管受感染病例数少影响,检测差异的能力有限,但我们发现,可检测到药物的血清转化者的序列比安慰剂或未坚持服药的血清转化者的序列更具同质性。