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Broadly Neutralizing Anti-HIV Antibodies Prevent HIV Infection of Mucosal Tissue Ex Vivo

机译:广泛中和抗HIV抗体可防止粘膜组织的艾滋病毒感染

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Broadly neutralizing monoclonal antibodies (nAbs) specific for HIV are being investigated for use in HIV prevention. Due to their ability to inhibit HIV attachment to and entry into target cells, nAbs may be suitable for use as topical HIV microbicides. As such, they would present an alternative intervention for individuals who may not benefit from using antiretroviral-based products for HIV prevention. We theorize that nAbs can inhibit viral transmission through mucosal tissue, thus reducing the incidence of HIV infection. The efficacy of the PG9, PG16, VRC01, and 4E10 antibodies was evaluated in an ex vivo human model of mucosal HIV transmission. nAbs reduced HIV transmission, causing 1.5- to 2-log(10) reductions in HIV replication in ectocervical tissues and approximate to 3-log(10) reductions in HIV replication in colonic tissues over 21 days. These antibodies demonstrated greater potency in colonic tissues, with a 50-fold higher dose being required to reduce transmission in ectocervical tissues. Importantly, nAbs retained their potency and reduced viral transmission in the presence of whole semen. No changes in tissue viability or immune activation were observed in colonic or ectocervical tissue after nAb exposure. Our data suggest that topically applied nAbs are safe and effective against HIV infection of mucosal tissue and support further development of nAbs as a topical microbicide that could be used for anal as well as vaginal protection.
机译:正在研究对HIV的宽度中和单克隆抗体(NABs)用于预防艾滋病毒。由于它们能够抑制艾滋病毒附着和进入靶细胞的能力,Nabs可以适合用作局部HIV杀微生物剂。因此,它们将为可能无法使用基于抗逆转录病毒的产品进行艾滋病毒预防的替代干预。我们理论发现NAB可以通过粘膜组织抑制病毒速度,从而降低HIV感染的发生率。在粘膜HIV透射的前体内人模型中评价PG9,PG16,VRCO1和4E10抗体的功效。 NABs降低了HIV透射,导致截断组织中的艾滋病毒复制中的1.5-至2-逻辑(10)减少,并在21天内在结肠组织中的HIV复制中的3-逻辑(10)减少。这些抗体在结肠组织中表现出更大的效力,需要50倍的剂量,以减少各种截障组织中的透射。重要的是,NABs在整个精液存在下保留了它们的效力并降低了病毒传播。在NAB暴露后,在结肠癌或地间截障组织中没有观察组织活力或免疫活化的变化。我们的数据表明,局部施用的Nabs对粘膜组织的HIV感染安全有效,并支持NAB的进一步发展作为可用于肛门和阴道保护的局部微生物剂。

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