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Antibody and TLR7 agonist delay viral rebound in SHIV-infected monkeys

机译:抗体和TLR7激动剂延迟SHIV感染猴子的病毒反弹

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The latent viral reservoir is the critical barrier for the development of a cure for HIV-1 infection. Previous studies have shown direct antiviral activity of potent HIV-1 Env-specific broadly neutralizing antibodies (bNAbs) administered when antiretroviral therapy (ART) was discontinued, but it remains unclear whether bNAbs can target the viral reservoir during ART. Here we show that administration of the V3 glycan-dependent bNAb PGT121 together with the Toll-like receptor 7 (TLR7) agonist vesatolimod (GS-9620) during ART delayed viral rebound following discontinuation of ART in simian-human immunodeficiency virus (SHIV) -SF162P3-infected rhesus monkeys in which ART was initiated during early acute infection. Moreover, in the subset of monkeys that were treated with both PGT121 and GS-9620 and that did not show viral rebound after discontinuation of ART, adoptive transfer studies and CD8 -depletion studies also did not reveal virus. These data demonstrate the potential of bNAb administration together with innate immune stimulation as a possible strategy for targeting the viral reservoir.
机译:潜在的病毒库是开发治疗HIV-1感染的关键障碍。先前的研究表明,停用抗逆转录病毒疗法(ART)后,所用的有效HIV-1 Env特异性中和抗体(bNAb)具有直接的抗病毒活性,但尚不清楚bNAbs是否可以在ART期间靶向病毒库。在这里,我们显示了在ART期间施用V3聚糖依赖性bNAb PGT121和Toll样受体7(TLR7)激动剂vesatolimod(GS-9620)可以在猿猴-人免疫缺陷病毒(SHIV)中终止ART后延缓病毒反弹- SF162P3感染的恒河猴,在早期急性感染过程中开始进行ART。此外,在接受PGT121和GS-9620治疗的猴子亚群中,ART终止后未显示病毒反弹,过继转移研究和CD8耗竭研究也未发现病毒。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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