Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, USA.
Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
Nat Rev Immunol. 2023 Mar;23(3):142-158. doi: 10.1038/s41577-022-00753-w. Epub 2022 Aug 12.
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.
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。