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Antibody and TLR7 Agonist Delay Viral Rebound in SHIV-Infected Monkeys

机译:SHIV感染的猴子中的抗体和TLR7激动剂延迟病毒反弹。

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摘要

The latent viral reservoir is the critical barrier for the development of an HIV-1 cure. Previous studies have shown that potent HIV-1 Env-specific broadly neutralizing antibodies (bNAbs) administered at the time of antiretroviral therapy (ART) discontinuation can exert direct antiviral effects, but whether bNAbs can target the viral reservoir during ART suppression remains unknown. Here we show that the V3 glycan-dependent bNAb PGT121 together with the TLR7 agonist vesatolimod (GS-9620) administered during ART suppression delayed viral rebound following ART discontinuation in SHIV-SF162P3-infected rhesus monkeys that initiated ART during early acute infection. Moreover, the subset of PGT121+GS-9620 treated monkeys that did not show viral rebound following ART discontinuation also did not reveal virus by highly sensitive adoptive transfer and CD8 depletion studies. These data demonstrate the potential of bNAb administration together with innate immune stimulation as a possible strategy to target the viral reservoir.
机译:潜在的病毒库是开发HIV-1疗法的关键障碍。先前的研究表明,在停用抗逆转录病毒疗法(ART)时给予有效的HIV-1 Env特异的广泛中和抗体(bNAb)可以发挥直接的抗病毒作用,但是在抑制ART的过程中bNAbs是否可以靶向病毒库尚不清楚。在这里,我们显示V3聚糖依赖性bNAb PGT121以及在ART抑制期间施用的TLR7激动剂vesatolimod(GS-9620)可以在SHIV-SF162P3感染的恒河猴中终止ART中断后病毒反弹,而在早期急性感染期间启动ART。而且,经高度敏感的过继转移和CD8耗竭研究,经PGT121 + GS-9620处理的猴子的亚组在ART停用后未显示病毒反弹,也未显示病毒。这些数据证明了将bNAb连同先天性免疫刺激一起作为靶向病毒库的可能策略的潜力。

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