| Literature DB >> 34919814 |
Jing Xue1, Huihui Chong2, Yuanmei Zhu2, Jingjing Zhang3, Ling Tong3, Jiahan Lu3, Ting Chen3, Zhe Cong3, Qiang Wei4, Yuxian He5.
Abstract
Two HIV fusion-inhibitory lipopeptides (LP-97 and LP-98) were designed with highly potent, long-acting antiviral activity. Monotherapy using a low dose of LP-98 sharply reduced viral loads and maintained long-term viral suppression in 21 SHIVSF162P3-infected rhesus macaques. We found that five treated monkeys achieved potential posttreatment control (PTC) efficacy and had lower viral DNA in deep lymph nodes, whereas monkeys with a stable viral rebound had higher viral DNA in superficial lymph nodes. The tissues of PTC monkeys exhibited significantly decreased quantitative viral outgrowth and fewer PD-1+ central memory CD4+ T cells, and CD8+ T cells contributed to virologic control efficacy. Moreover, LP-98 administrated as a pre-exposure prophylaxis (PrEP) provided complete protection against SHIVSF162P3 and SIVmac239 infections in 51 monkeys via intrarectal, intravaginal, or intravenous challenge. In conclusion, our lipopeptides exhibit high potential as an efficient HIV treatment or prevention strategy.Entities:
Keywords: CD8(+) T cells; HIV; PTC; PrEP; fusion inhibitor; lipopeptide; membrane fusion; posttreatment control; pre-exposure prophylaxis; viral reservoir
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Year: 2021 PMID: 34919814 DOI: 10.1016/j.cell.2021.11.032
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582