Neutralization and beyond: Antibodies and HIV-1 acquisition.

Current Topics In Virology Pub Date : 2018-01-01
Allison S Thomas, Melissa Ghulam-Smith, Manish Sagar
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Abstract

It is widely accepted that an effective HIV-1 preventative vaccine must elicit antibodies that can block virus acquisition. Although, anti-HIV-1 broadly neutralizing antibodies (bnAbs) have been isolated, unfortunately, no vaccine immunogens have been designed that can elicit these bnAbs in uninfected at-risk individuals. Some studies have suggested that other antibody functionalities, besides neutralization, such as antibody-dependent cellular cytotoxicity (ADCC), may prevent HIV-1 acquisition. In contrast to bnAbs, ADCC-inducing antibodies may be more amenable to elicitation by current vaccine technologies. This review will provide clarity about the role of nAbs and ADCC-inducing antibodies in preventing transmission, highlight mechanisms that potentially explain how ADCC-mediating antibodies may work, and speculate about the generation of these novel protective antibodies. Anti-HIV-1 ADCC-inducing antibodies may provide a new avenue for developing an effective HIV-1 vaccine.

中和与超越:抗体与 HIV-1 感染。
人们普遍认为,有效的 HIV-1 预防性疫苗必须能激发出阻止病毒感染的抗体。虽然已经分离出了抗 HIV-1 的广泛中和抗体(bnAbs),但遗憾的是,还没有设计出能在未感染的高危人群中诱导出这些 bnAbs 的疫苗免疫原。一些研究表明,除了中和抗体外,其他抗体功能(如抗体依赖性细胞毒性(ADCC))也可防止 HIV-1 感染。与 bnAbs 相比,ADCC 诱导抗体可能更适于通过当前的疫苗技术激发。本综述将阐明nAbs和ADCC诱导抗体在预防传播中的作用,强调可能解释ADCC介导抗体如何发挥作用的机制,并推测这些新型保护性抗体的产生。抗HIV-1 ADCC诱导抗体可能为开发有效的HIV-1疫苗提供一条新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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