偏肺病毒
抗体
病毒学
变性肺病毒
多克隆抗体
免疫学
单克隆抗体
免疫系统
生物
原罪
呼吸道感染
呼吸系统
血凝素(流感)
抗原漂移
解剖
作者
Scott A. Rush,Gurpreet Brar,Ching‐Lin Hsieh,Émilie Chautard,Jennifer N. Rainho-Tomko,Chris D. Slade,Christine A. Bricault,Ana Kume,James Kearns,Rachel Groppo,Sophia T. Mundle,Linong Zhang,Danilo R. Casimiro,Tong‐Ming Fu,Joshua M. DiNapoli,Jason S. McLellan
出处
期刊:Cell Reports
[Elsevier]
日期:2022-09-01
卷期号:40 (12): 111399-111399
被引量:17
标识
DOI:10.1016/j.celrep.2022.111399
摘要
Human metapneumovirus (hMPV) is a major cause of acute respiratory infections in infants and older adults, for which no vaccines or therapeutics are available. The viral fusion (F) glycoprotein is required for entry and is the primary target of neutralizing antibodies; however, little is known about the humoral immune response generated from natural infection. Here, using prefusion-stabilized F proteins to interrogate memory B cells from two older adults, we obtain over 700 paired non-IgM antibody sequences representing 563 clonotypes, indicative of a highly polyclonal response. Characterization of 136 monoclonal antibodies reveals broad recognition of the protein surface, with potently neutralizing antibodies targeting each antigenic site. Cryo-EM studies further reveal two non-canonical sites and the molecular basis for recognition of the apex of hMPV F by two prefusion-specific neutralizing antibodies. Collectively, these results provide insight into the humoral response to hMPV infection in older adults and will help guide vaccine development.
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