Division of HIV/AIDS Prevention, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA 30329, United States.
Rollins School of Public Health, Emory University, Atlanta, GA, United States.
EBioMedicine. 2020 Aug;58:102894. doi: 10.1016/j.ebiom.2020.102894. Epub 2020 Jul 21.
Daily oral pre- or post-exposure prophylaxis (PrEP or PEP) is highly effective in preventing HIV infection. However, many people find it challenging to adhere to a daily oral regimen. Chemoprophylaxis with single oral doses of antiretroviral drugs taken before or after sex may better adapt to changing or unanticipated sexual practices and be a desirable alternative to daily PrEP or PEP. We investigated willingness to use a single oral pill before or after sex among men who have sex with men (MSM) and assessed the biological efficacy of a potent antiretroviral combination containing elvitegravir (EVG), emtricitabine (FTC), and tenofovir alafenamide (TAF).
Data on willingness to use single-dose PrEP or PEP were obtained from the 2017 cycle of the American Men's Internet Survey (AMIS), an annual online behavioral surveillance survey of MSM in the United States. Antiretroviral drug levels were measured in humans and macaques to define drug distribution in rectal tissue and identify clinically relevant doses for macaque modeling studies. The biological efficacy of a single dose of FTC/TAF/EVG as PrEP or PEP was investigated using a repeat-challenge macaque model of rectal HIV infection.
Through pharmacokinetic assessment in humans and macaques we found that EVG penetrates and concentrates in rectal tissues supporting its addition to FTC/TAF to boost and extend chemoprophylactic activity. Efficacy estimates for a single oral dose given to macaques 4h before or 2h after SHIV exposure was 91•7%[35•7%-98•9%] and 100%, respectively, compared to 80•1%[13•9%-95•4%] and 64•6%[-19•4%-89•5%] when single doses were given 6 and 24h post challenge, respectively. A two-dose regimen at 24h and 48h after exposure was also protective [77•1%[1•7%-94•7%].
Informed by user willingness, human and macaque pharmacokinetic data, and preclinical efficacy we show that single-dose prophylaxis before or after sex is a promising HIV prevention strategy. Carefully designed clinical trials are needed to determine if any of these strategies will be effective in humans.
Funded by CDC intramural funds, CDC contract HCVJCG2-2016-03948 (to CFK), and a grant from the MAC AIDS Fund and by the National Institutes of Health [P30AI050409] - the Emory Center for AIDS Research (to MZ and TS).
每日口服暴露前或暴露后预防(PrEP 或 PEP)在预防 HIV 感染方面非常有效。然而,许多人发现很难坚持每日口服治疗方案。在性行为前或后服用单次口服剂量的抗逆转录病毒药物进行化学预防可能更适合不断变化或意外的性行为,并成为每日 PrEP 或 PEP 的理想替代方案。我们调查了男男性行为者(MSM)对性行为前或后使用单次口服药丸的意愿,并评估了含有艾维雷格(EVG)、恩曲他滨(FTC)和替诺福韦艾拉酚胺(TAF)的强效抗逆转录病毒组合的生物疗效。
通过 2017 年美国男性互联网调查(AMIS)的循环数据,这是一项针对美国 MSM 的年度在线行为监测调查,获得了对使用单次剂量 PrEP 或 PEP 的意愿的数据。在人类和猕猴中测量了抗逆转录病毒药物的水平,以确定直肠组织中的药物分布,并确定猕猴模型研究中具有临床意义的剂量。使用直肠 HIV 感染的猕猴重复挑战模型研究了 FTC/TAF/EVG 作为 PrEP 或 PEP 的单次剂量的生物学疗效。
通过对人类和猕猴的药代动力学评估,我们发现 EVG 渗透并集中在直肠组织中,支持将其添加到 FTC/TAF 中以增强和延长化学预防活性。与单剂量在暴露后 6 小时和 24 小时给药时分别为 80.1%[13.9%-95.4%]和 64.6%[-19.4%-89.5%]相比,猕猴在暴露前 4 小时或暴露后 2 小时给予单剂量时,估计的功效分别为 91.7%[35.7%-98.9%]和 100%。暴露后 24 小时和 48 小时给予两剂方案也具有保护作用[77.1%[1.7%-94.7%]。
根据用户意愿、人类和猕猴药代动力学数据以及临床前疗效,我们表明性行为前或后单次预防是一种有前途的 HIV 预防策略。需要精心设计临床试验来确定这些策略中的任何一种是否对人类有效。
美国疾病控制与预防中心内部资金、美国疾病控制与预防中心合同 HCVJCG2-2016-03948(给 CFK)以及 MAC AIDS 基金和美国国立卫生研究院的资助[P30AI050409] - 埃默里艾滋病研究中心(给 MZ 和 TS)。