Cheung Crystal Sao-Fong, Gorman Jason, Andrews Sarah F, Rawi Reda, Reveiz Mateo, Shen Chen-Hsiang, Wang Yiran, Harris Darcy R, Nazzari Alexandra F, Olia Adam S, Raab Julie, Teng I-Ting, Verardi Raffaello, Wang Shuishu, Yang Yongping, Chuang Gwo-Yu, McDermott Adrian B, Zhou Tongqing, Kwong Peter D
Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Structure. 2022 Jul 7;30(7):993-1003.e6. doi: 10.1016/j.str.2022.04.003. Epub 2022 Apr 29.
Several influenza antibodies with broad group 2 neutralization have recently been isolated. Here, we analyze the structure, class, and binding of one of these antibodies from an H7N9 vaccine trial, 315-19-1D12. The cryo-EM structure of 315-19-1D12 Fab in complex with the hemagglutinin (HA) trimer revealed the antibody to recognize the helix A region of the HA stem, at the supersite of vulnerability recognized by group 1-specific and by cross-group-neutralizing antibodies. 315-19-1D12 was derived from HV1-2 and KV2-28 genes and appeared to form a new antibody class. Bioinformatic analysis indicated its group 2 neutralization specificity to be a consequence of four key residue positions. We specifically tested the impact of the group 1-specific N33 glycan, which decreased but did not abolish group 2 binding of 315-19-1D12. Overall, this study highlights the recognition of a broad group 2-neutralizing antibody, revealing unexpected diversity in neutralization specificity for antibodies that recognize the HA stem supersite.
最近分离出了几种具有广泛2组中和活性的流感抗体。在此,我们分析了来自一项H7N9疫苗试验的其中一种抗体315-19-1D12的结构、类别和结合情况。315-19-1D12 Fab与血凝素(HA)三聚体复合物的冷冻电镜结构显示,该抗体识别HA茎干的A螺旋区域,位于1组特异性抗体和跨组中和抗体识别的超易损位点。315-19-1D12源自HV1-2和KV2-28基因,似乎形成了一种新的抗体类别。生物信息学分析表明,其2组中和特异性是四个关键残基位置的结果。我们专门测试了1组特异性N33聚糖的影响,它降低了但并未消除315-19-1D12与2组的结合。总体而言,这项研究突出了一种广泛的2组中和抗体的识别,揭示了识别HA茎干超易损位点的抗体在中和特异性方面意想不到的多样性。