Human neutralizing antibodies target a conserved lateral patch on H7N9 hemagglutinin head

• Published in: Nature communications Vol. 15; no. 1; pp. 4505 - 14
• Main Authors: Jia, Manxue, Zhao, Hanjun, Morano, Nicholas C., Lu, Hong, Lui, Yin-Ming, Du, Haijuan, Becker, Jordan E., Yuen, Kwok-Yung, Ho, David D., Kwong, Peter D., Shapiro, Lawrence, To, Kelvin Kai-Wang, Wu, Xueling
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 27.05.2024; Nature Publishing Group; Nature Portfolio
• Subjects: 101/28; 13/1; 13/106; 13/109; 13/31; 38/23; 38/77; 631/250/2152/2153/1291; 631/326/596/1578; 631/45/535/1258/1259; 82/16; 82/80; 82/83; Animals; Antibodies; Antibodies, Monoclonal - immunology; Antibodies, Neutralizing - immunology; Antibodies, Viral - immunology; Avian flu; Cryoelectron Microscopy; Epitopes; Epitopes - immunology; Female; Females; Hemagglutinin Glycoproteins, Influenza Virus - immunology; Hemagglutinins; Humanities and Social Sciences; Humans; Hydrophobicity; Influenza; Influenza A; Influenza A Virus, H7N9 Subtype - immunology; Influenza, Human - immunology; Influenza, Human - prevention & control; Influenza, Human - virology; Mice; Mice, Inbred BALB C; Monoclonal antibodies; multidisciplinary; Neutralization; Neutralizing; Orthomyxoviridae Infections - immunology; Orthomyxoviridae Infections - prevention & control; Orthomyxoviridae Infections - virology; Science; Science (multidisciplinary); Sequence analysis
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-024-48758-4

Avian influenza A virus H7N9 causes severe human infections with >30% fatality. Currently, there is no H7N9-specific prevention or treatment for humans. Here, from a 2013 H7N9 convalescent case in Hong Kong, we isolate four hemagglutinin (HA)-reactive monoclonal antibodies (mAbs), with three directed to the globular head domain (HA1) and one to the stalk domain (HA2). Two clonally related HA1-directed mAbs, H7.HK1 and H7.HK2, potently neutralize H7N9 and protect female mice from lethal H7N9/AH1 challenge. Cryo-EM structures reveal that H7.HK1 and H7.HK2 bind to a β14-centered surface and disrupt the 220-loop that makes hydrophobic contacts with sialic acid on an adjacent protomer, thereby blocking viral entry. Sequence analysis indicates the lateral patch targeted by H7.HK1 and H7.HK2 to be conserved among influenza subtypes. Both H7.HK1 and H7.HK2 retain HA1 binding and neutralization capacity to later H7N9 isolates from 2016–2017, consistent with structural data showing that the antigenic mutations during this timeframe occur at their epitope peripheries. The HA2-directed mAb H7.HK4 lacks neutralizing activity but when used in combination with H7.HK2 moderately augments female mouse protection. Overall, our data reveal antibodies to a conserved lateral HA1 supersite that confer neutralization, and when combined with a HA2-directed non-neutralizing mAb, augment protection. Here the authors isolate two human antibodies, H7.HK1 and H7.HK2, that achieve broad and potent neutralization against H7N9 influenza by targeting a distinct lateral patch on the hemagglutinin head, thus making them favorable to complement other antibodies for combination therapy.