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Approaches to the induction of HIV broadly neutralizing antibodies

机译:艾滋病毒广泛中和抗体的诱导方法

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Purpose of reviewA vaccine that elicits antibody responses that can neutralize the diversity of HIV clades has not yet been achieved, and is a major focus of HIV vaccine research. Here, we provide an update on the barriers to eliciting such antibodies, and how advances in immunogen design may circumvent these roadblocks, focusing on data published in the last year.Recent findingsStudies of how broadly neutralizing antibodies (bNAbs) develop in HIV-infected donors continue to produce key insights, suggesting that for some viral targets there are common pathways to developing breadth. Germline-targeting strategies, that aim to recruit rare precursors of bNAbs, have shown promise in immunogenicity studies, and structural biology has led to advances in immunogen design. Mapping of strain-specific tier 2 vaccine responses has highlighted the challenges that remain in driving antibodies toward breadth.SummaryElucidation of the HIV envelope structure, together with an understanding of how bNAbs emerge in vivo has guided the design of new immunogens and vaccine strategies that show promise for eliciting protective antibodies.
机译:审查目的尚未实现引起中和HIV进化枝多样性的抗体反应的疫苗,这是HIV疫苗研究的主要重点。在这里,我们提供了有关引出此类抗体的障碍的最新信息,以及免疫原设计的进展如何绕开这些障碍的方法,重点是去年发表的数据。继续产生关键见解,这表明对于某些病毒靶标,存在发展广度的常见途径。旨在招募稀有bNAb前体的生殖细胞靶向策略在免疫原性研究中显示出了希望,结构生物学已导致免疫原设计的进步。菌株特异性2级疫苗反应的定位图突出显示了驱动抗体趋向广度的挑战。总结对HIV包膜结构的阐明以及对bNAb在体内如何出现的理解指导了设计新的免疫原和疫苗策略的研究有望引发保护性抗体。

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