MOE/NHC/CAMS Key Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Front Med. 2020 Apr;14(2):149-159. doi: 10.1007/s11684-020-0764-y. Epub 2020 Apr 1.
Influenza causes seasonal outbreaks yearly and unpredictable pandemics with high morbidity and mortality rates. Despite significant efforts to address influenza, it remains a major threat to human public health. This issue is partially due to the lack of antiviral drugs with potent antiviral activity and broad reactivity against all influenza virus strains and the rapid emergence of drug-resistant variants. Moreover, designing a universal influenza vaccine that is sufficiently immunogenic to induce universal antibodies is difficult. Some novel epitopes hidden in the hemagglutinin (HA) trimeric interface have been discovered recently, and a number of antibodies targeting these epitopes have been found to be capable of neutralizing a broad range of influenza isolates. These findings may have important implications for the development of universal influenza vaccines and antiviral drugs. In this review, we focused on the antibodies targeting these newly discovered epitopes in the HA domain of the influenza virus to promote the development of universal anti-influenza antibodies or vaccines and extend the discovery to other viruses with similar conformational changes in envelope proteins.
流感每年都会引发季节性爆发和难以预测的大流行,导致高发病率和死亡率。尽管人们为应对流感做出了巨大努力,但它仍然是人类公共卫生的主要威胁。造成这种情况的部分原因是缺乏具有强大抗病毒活性和广泛针对所有流感病毒株的反应性的抗病毒药物,以及耐药变异株的快速出现。此外,设计一种具有足够免疫原性以诱导通用抗体的通用流感疫苗也很困难。最近发现了一些隐藏在血凝素 (HA) 三聚体界面中的新型表位,并且发现了许多针对这些表位的抗体能够中和广泛的流感分离株。这些发现可能对开发通用流感疫苗和抗病毒药物具有重要意义。在这篇综述中,我们重点介绍了针对流感病毒 HA 结构域中这些新发现表位的抗体,以促进通用抗流感抗体或疫苗的开发,并将这一发现扩展到其他具有类似包膜蛋白构象变化的病毒。