Public Health - Seattle & King County, Seattle, Washington, United States of America.
Department of Epidemiology, University of Washington, Seattle, Washington, United States of America.
PLoS One. 2022 Aug 29;17(8):e0272958. doi: 10.1371/journal.pone.0272958. eCollection 2022.
The risk of HIV pre-exposure prophylaxis (PrEP) failure with sufficient medication adherence is extremely low but has occurred due to transmission of a viral strain with mutations conferring resistance to PrEP components tenofovir (TDF) and emtricitabine (FTC). The extent to which such strains are circulating in the population is unknown.
We used HIV surveillance data to describe primary and overall TDF/FTC resistance and concurrent viremia among people living with HIV (PLWH). HIV genotypes conducted for clinical purposes are reported as part of HIV surveillance. We examined the prevalence of HIV strains with mutations conferring intermediate to high level resistance to TDF/FTC, defining primary resistance (predominantly K65R and M184I/V mutations) among sequences reported within 3 months of HIV diagnosis and total resistance for sequences reported at any time. We examined trends in primary resistance during 2010-2019 and total resistance among all PLWH in 2019. We also monitored resistance with viremia (≥1,000 copies/mL) at the end of 2019 among PLWH.
Between 2010 and 2019, 2,172 King County residents were diagnosed with HIV; 1,557 (72%) had a genotypic resistance test within three months; three (0.2%) had primary TDF/FTC resistance with both K65R and M184I/V mutations. Adding isolated resistance for each drug resulted in 0.3% with primary TDF resistance and 0.8% with primary FTC resistance. Of 7,056 PLWH in 2019, 4,032 (57%) had genotype results, 241 (6%) had TDF/FTC resistance and 15 (0.4% of those with a genotype result) had viremia and TDF/FTC resistance.
Primary resistance and viremia combined with TDF/FTC resistance are uncommon in King County. Monitoring trends in TDF/FTC resistance coupled with interventions to help ensure PLWH achieve and maintain viral suppression may help ensure that PrEP failure remains rare.
充分的药物依从性下,HIV 暴露前预防(PrEP)失败的风险极低,但由于传播对 PrEP 成分替诺福韦(TDF)和恩曲他滨(FTC)具有耐药性的病毒株,这种情况已经发生。目前尚不清楚此类病毒株在人群中的传播程度。
我们使用 HIV 监测数据描述了 HIV 感染者(PLWH)中原发性和总体 TDF/FTC 耐药性以及并发病毒血症。因临床目的进行的 HIV 基因型检测结果作为 HIV 监测的一部分进行报告。我们检查了具有中高度 TDF/FTC 耐药性突变的 HIV 株的流行率,将报告的 HIV 诊断后 3 个月内的序列中的原发性耐药(主要为 K65R 和 M184I/V 突变)和任何时候报告的总耐药定义为原发性耐药。我们检查了 2010 年至 2019 年期间原发性耐药的趋势以及 2019 年所有 PLWH 中的总耐药性。我们还监测了 2019 年底 PLWH 中病毒载量(≥1,000 拷贝/ml)与耐药性的关系。
2010 年至 2019 年间,金县有 2172 名居民被诊断出 HIV 感染;1557 人(72%)在三个月内进行了基因耐药性检测;其中 3 人(0.2%)同时具有 K65R 和 M184I/V 突变的原发性 TDF/FTC 耐药性。每种药物的单独耐药性导致 0.3%的原发性 TDF 耐药和 0.8%的原发性 FTC 耐药。2019 年,7056 名 PLWH 中有 4032 人(57%)有基因型结果,241 人(6%)有 TDF/FTC 耐药性,15 人(有基因型结果的人占 0.4%)有病毒血症和 TDF/FTC 耐药性。
金县原发性耐药和病毒血症合并 TDF/FTC 耐药性并不常见。监测 TDF/FTC 耐药性的趋势,并结合干预措施,以帮助确保 PLWH 实现并维持病毒抑制,这可能有助于确保 PrEP 失败仍然罕见。