Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Division of Infectious Diseases, Brigham and Women's Hospital and Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Nature. 2022 Jan;601(7894):612-616. doi: 10.1038/s41586-021-04279-4. Epub 2021 Dec 7.
Because no currently available vaccine can prevent HIV infection, pre-exposure prophylaxis (PrEP) with antiretrovirals (ARVs) is an important tool for combating the HIV pandemic. Long-acting ARVs promise to build on the success of current PrEP strategies, which must be taken daily, by reducing the frequency of administration. GS-CA1 is a small-molecule HIV capsid inhibitor with picomolar antiviral potency against a broad array of HIV strains, including variants resistant to existing ARVs, and has shown long-acting therapeutic potential in a mouse model of HIV infection. Here we show that a single subcutaneous administration of GS-CA1 provides long-term protection against repeated rectal simian-human immunodeficiency virus (SHIV) challenges in rhesus macaques. Whereas all control animals became infected after 15 weekly challenges, a single 300 mg kg dose of GS-CA1 provided per-exposure infection risk reduction of 97% for 24 weeks. Pharmacokinetic analysis showed a correlation between GS-CA1 plasma concentration and protection from SHIV challenges. GS-CA1 levels greater than twice the rhesus plasma protein-adjusted 95% effective concentration conferred 100% protection in this model. These proof-of-concept data support the development of capsid inhibitors as a novel long-acting PrEP strategy in humans.
由于目前尚无预防 HIV 感染的疫苗,因此使用抗逆转录病毒药物(ARV)进行暴露前预防(PrEP)是抗击 HIV 大流行的重要工具。长效 ARV 有望在当前 PrEP 策略的基础上取得成功,这些策略必须每天服用,以减少给药频率。GS-CA1 是一种小分子 HIV 衣壳抑制剂,对广泛的 HIV 株具有皮摩尔级别的抗病毒效力,包括对现有 ARV 耐药的变异株,并且在 HIV 感染的小鼠模型中表现出长效治疗潜力。在这里,我们表明,单次皮下注射 GS-CA1 可提供针对恒河猴重复直肠猴免疫缺陷病毒(SHIV)挑战的长期保护。所有对照动物在 15 次每周挑战后均被感染,而单次 300mg/kg 的 GS-CA1 剂量可将暴露后感染风险降低 97%,持续 24 周。药代动力学分析表明,GS-CA1 血浆浓度与 SHIV 挑战的保护之间存在相关性。在该模型中,GS-CA1 水平高于恒河猴血浆蛋白调整的 95%有效浓度的两倍可提供 100%的保护。这些概念验证数据支持将衣壳抑制剂作为人类新型长效 PrEP 策略进行开发。