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诱导广泛中和抗体的 HIV-1 疫苗策略。

Strategies for HIV-1 vaccines that induce broadly neutralizing antibodies.

机构信息

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, USA.

Department of Medicine, Duke University School of Medicine, Durham, NC, USA.

出版信息

Nat Rev Immunol. 2023 Mar;23(3):142-158. doi: 10.1038/s41577-022-00753-w. Epub 2022 Aug 12.

Abstract

After nearly four decades of research, a safe and effective HIV-1 vaccine remains elusive. There are many reasons why the development of a potent and durable HIV-1 vaccine is challenging, including the extraordinary genetic diversity of HIV-1 and its complex mechanisms of immune evasion. HIV-1 envelope glycoproteins are poorly recognized by the immune system, which means that potent broadly neutralizing antibodies (bnAbs) are only infrequently induced in the setting of HIV-1 infection or through vaccination. Thus, the biology of HIV-1-host interactions necessitates novel strategies for vaccine development to be designed to activate and expand rare bnAb-producing B cell lineages and to select for the acquisition of critical improbable bnAb mutations. Here we discuss strategies for the induction of potent and broad HIV-1 bnAbs and outline the steps that may be necessary for ultimate success.

摘要

经过近四十年的研究,一种安全有效的 HIV-1 疫苗仍然难以捉摸。HIV-1 疫苗的开发具有挑战性有很多原因,包括 HIV-1 的巨大遗传多样性及其复杂的免疫逃逸机制。HIV-1 包膜糖蛋白不能被免疫系统很好地识别,这意味着在 HIV-1 感染或通过疫苗接种的情况下,只有很少的强效广谱中和抗体(bnAbs)被诱导产生。因此,HIV-1-宿主相互作用的生物学需要设计新的疫苗开发策略,以激活和扩大罕见的产生 bnAb 的 B 细胞谱系,并选择获得关键的不可能的 bnAb 突变。在这里,我们讨论了诱导强效广谱 HIV-1 bnAbs 的策略,并概述了最终取得成功可能需要采取的步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae44/9372928/a061f2fa4511/41577_2022_753_Fig1_HTML.jpg

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