脂肽
药代动力学
病毒
最大值
病毒复制
病毒学
药理学
医学
病毒载量
CD8型
免疫学
生物
免疫系统
遗传学
细菌
作者
Jing Xue,Yuanmei Zhu,Chenbo Yang,Xiaosheng Liu,Rui Hou,Wei Wang,Huihui Chong,Zhe Cong,Jingjing Zhang,Ling Tong,Jiahan Lu,Peiwen Liu,Ting Chen,Na Li,Qiang Wei,Yuxian He
出处
期刊:Cell Reports
[Cell Press]
日期:2025-09-01
卷期号:44 (9): 116228-116228
标识
DOI:10.1016/j.celrep.2025.116228
摘要
LP-98 is a lipopeptide HIV fusion inhibitor showing strong treatment and pre-exposure prophylaxis efficacies in non-human primates. In this study, we further characterized its pharmacokinetics, long-lasting antiviral activity, and post-exposure prophylaxis (PEP) efficacy using 62 macaques. In cynomolgus macaques, LP-98 achieved high concentrations (Cmax) with a half-life (T1/2) of ∼31 h, and sustained an effective therapeutic concentration for two weeks post-injection. In chronically SHIVSF162P3-infected rhesus macaques (RMs), weekly or biweekly LP-98 monotherapy efficiently suppressed virus replication. In the PEP study, early LP-98 administration (weekly for 4 weeks) provided robust protection against SHIVSF162P3 infection through intrarectal and intravenous challenges. No viral DNA or replication-competent virus was detected in tissues from protected RMs, even after CD8+ T cell depletion. Transcriptomic analyses revealed the potential immunomodulatory effects of LP-98 treatment. Collectively, our results demonstrate the importance of LP-98 for HIV prevention and treatment and facilitate its current clinical studies.
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