Grant Robert M, Liegler Teri, Defechereux Patricia, Kashuba Angela D M, Taylor Douglas, Abdel-Mohsen Mohamed, Deese Jennifer, Fransen Katrien, De Baetselier Irith, Crucitti Tania, Bentley Gordon, Agingu Walter, Ahmed Khatija, Damme Lut Van
AIDS. 2015 Jan 28;29(3):331-7. doi: 10.1097/QAD.0000000000000556.
Pre-exposure prophylaxis (PrEP) with daily oral emtricitabine (FTC)/tenofovir disoproxil fumarate may select for drug resistance if there is low adherence.
Plasma viral HIV-1 RNA level, CD4+ T-cell counts, and drug resistance were evaluated among seroconverting women in the FEM-PrEP trial (clinicaltrials.gov NCT00625404) using standard clinical tests, allele-specific PCR (ASPCR), and by deep sequencing. Tenofovir, FTC, and their intracellular metabolites were measured in plasma and cells.
There was no difference in plasma HIV-1 RNA level or CD4+ cell count among seroconverters in the active arm versus those receiving placebo. Tenofovir resistance was not observed. FTC resistance was detected using clinical assays in five seroconverters (four in the active arm and one in the placebo arm); two in the active arm occurred among women having moderate concentrations of PrEP drugs in the blood. The first evidence of infection occurred at the first postenrollment visit in three of the four with FTC resistance, although none had detectable viral nucleic acids at enrollment. FTC-resistant minor variants were detected in an additional four seroconverters (one in the active arm and three in the placebo arm).
Drug resistance detected during ineffective PrEP use had characteristics suggesting transmitted infection or incubating infection prior to starting PrEP.
如果依从性低,每日口服恩曲他滨(FTC)/替诺福韦酯进行暴露前预防(PrEP)可能会导致耐药性产生。
在FEM-PrEP试验(clinicaltrials.gov NCT00625404)中,使用标准临床检测、等位基因特异性PCR(ASPCR)和深度测序,对血清转化女性的血浆HIV-1 RNA水平、CD4 + T细胞计数和耐药性进行评估。检测血浆和细胞中的替诺福韦、FTC及其细胞内代谢产物。
活性治疗组血清转化者与接受安慰剂者相比,血浆HIV-1 RNA水平或CD4 +细胞计数无差异。未观察到替诺福韦耐药性。使用临床检测方法在5名血清转化者中检测到FTC耐药性(活性治疗组4名,安慰剂组1名);活性治疗组中有2例发生在血液中PrEP药物浓度中等的女性中。在4名FTC耐药者中的3名中,首次感染证据出现在入组后的首次随访中,尽管在入组时均未检测到病毒核酸。在另外4名血清转化者中检测到FTC耐药性次要变异体(活性治疗组1名,安慰剂组3名)。
在无效的PrEP使用期间检测到的耐药性具有提示在开始PrEP之前存在传播感染或潜伏感染的特征。