不断扩大的艾滋病毒抗体广泛中和。

IF 2.7 3区 医学 Q3 VIROLOGY
Laura E McCoy
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引用次数: 39

摘要

特别是在过去十年中,已经分离和描述了大量抗HIV的广泛中和抗体(bnAbs)。这种不断扩大的bnAbs阵列至关重要地导致了HIV包膜蛋白上新表位的鉴定,抗体可以通过该表位阻断广泛的HIV毒株。此外,这些研究已经对包膜蛋白上的这些易损位点产生了高分辨率的理解。他们还阐明了bnab抗体的作用机制,并提供了它们产生的B细胞本体的详细描述。然而,仍然不可能预测哪些艾滋病毒感染者将继续发展呼吸,也不可能通过免疫在人类中诱导中和广度。这篇综述的目的是讨论到目前为止获得的主要见解,并评估继续分离和表征新的bnAbs的需求。虽然新的表位可能仍有待发现,但进一步表征bnAb的一个更明确的可能好处是,可以更好地了解抗hiv免疫应答中bnAb发展的关键决策点。这反过来可能会导致如何通过免疫触发bnAbs的新见解,并更清楚地定义使用bnAbs作为治疗剂的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The expanding array of HIV broadly neutralizing antibodies.

The expanding array of HIV broadly neutralizing antibodies.

A large array of broadly neutralizing antibodies (bnAbs) against HIV have been isolated and described, particularly in the last decade. This continually expanding array of bnAbs has crucially led to the identification of novel epitopes on the HIV envelope protein via which antibodies can block a broad range of HIV strains. Moreover, these studies have produced high-resolution understanding of these sites of vulnerability on the envelope protein. They have also clarified the mechanisms of action of bnAbs and provided detailed descriptions of B cell ontogenies from which they arise. However, it is still not possible to predict which HIV-infected individuals will go onto develop breath nor is it possible to induce neutralization breadth by immunization in humans. This review aims to discuss the major insights gained so far and also to evaluate the requirement to continue isolating and characterizing new bnAbs. While new epitopes may remain to be uncovered, a clearer probable benefit of further bnAb characterization is a greater understanding of key decision points in bnAb development within the anti-HIV immune response. This in turn may lead to new insights into how to trigger bnAbs by immunization and more clearly define the challenges to using bnAbs as therapeutic agents.

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来源期刊
Retrovirology
Retrovirology 医学-病毒学
CiteScore
5.80
自引率
3.00%
发文量
24
审稿时长
>0 weeks
期刊介绍: Retrovirology is an open access, online journal that publishes stringently peer-reviewed, high-impact articles on host-pathogen interactions, fundamental mechanisms of replication, immune defenses, animal models, and clinical science relating to retroviruses. Retroviruses are pleiotropically found in animals. Well-described examples include avian, murine and primate retroviruses. Two human retroviruses are especially important pathogens. These are the human immunodeficiency virus, HIV, and the human T-cell leukemia virus, HTLV. HIV causes AIDS while HTLV-1 is the etiological agent for adult T-cell leukemia and HTLV-1-associated myelopathy/tropical spastic paraparesis. Retrovirology aims to cover comprehensively all aspects of human and animal retrovirus research.
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