McFadden William M, Faerch Mia, Kirby Karen A, Dick Robert A, Torbett Bruce E, Sarafianos Stefan G
Center for ViroScience and Cure, Laboratory of Biochemical Pharmacology, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA; Children's Healthcare of Atlanta, Atlanta, GA 30322, USA.
Center for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA 98101, USA.
Trends Mol Med. 2025 Feb 27. doi: 10.1016/j.molmed.2025.01.013.
Antiretroviral therapy (ART) impairs viral replication in people living with HIV (PLWH) by suppressing infection or spread. However, not all treatment strategies apply to preventive applications like pre-exposure prophylaxis (PrEP) for uninfected individuals. To prevent the establishment of HIV infection, PrEP must block viral replication either before, or at the stage of integration into the host genome. A promising PrEP approach under investigation utilizes lenacapavir (LEN), which targets the HIV-1 capsid protein (CA) potently before integration. LEN, a first-in-class antiretroviral, has shown high protective efficacy in the ongoing PURPOSE trials thus far. Here, we discuss clinical investigations of LEN, theoretical suitability of preclinical CA-binding antivirals in PrEP, and other key considerations for preventing HIV-1 infection by targeting the capsid.
抗逆转录病毒疗法(ART)通过抑制感染或传播来损害HIV感染者(PLWH)体内的病毒复制。然而,并非所有治疗策略都适用于预防应用,如针对未感染个体的暴露前预防(PrEP)。为了预防HIV感染的建立,PrEP必须在病毒整合到宿主基因组之前或在该阶段阻断病毒复制。正在研究的一种有前景的PrEP方法利用了来那卡韦(LEN),它在整合前有效地靶向HIV-1衣壳蛋白(CA)。LEN是一流的抗逆转录病毒药物,在目前正在进行的PURPOSE试验中已显示出高保护效力。在此,我们讨论LEN的临床研究、临床前CA结合抗病毒药物在PrEP中的理论适用性,以及通过靶向衣壳预防HIV-1感染的其他关键考虑因素。