病毒学
单克隆抗体
表位
生物
抗原性
神经氨酸酶
病毒
抗体
甲型流感病毒
抗原漂移
H5N1亚型流感病毒
大流行
H5N1基因结构
糖蛋白
体外
微生物学
免疫学
2019年冠状病毒病(COVID-19)
医学
分子生物学
传染病(医学专业)
生物化学
疾病
病理
作者
Lena Hansen,Meagan McMahon,Hannah L. Turner,Xueyong Zhu,Jackson S. Turner,Gabriel Ozorowski,Daniel Stadlbauer,Juha Vahokoski,Aaron J. Schmitz,Amena A. Rizk,Wafaa B. Alsoussi,Shirin Strohmeier,Wenli Yu,José Alberto Choreño-Parra,Luis Armando Jiménez-Álvarez,Alfredo Cruz‐Lagunas,Joaquı́n Zúñiga,Philip A. Mudd,Rebecca Jane Cox,Ian A. Wilson,Andrew B. Ward,Ali H. Ellebedy,Florian Krammer
出处
期刊:Immunity
[Elsevier]
日期:2023-08-01
卷期号:56 (8): 1927-1938.e8
被引量:7
标识
DOI:10.1016/j.immuni.2023.07.004
摘要
Summary
Neuraminidase (NA) is one of the two influenza virus surface glycoproteins, and antibodies that target it are an independent correlate of protection. However, our current understanding of NA antigenicity is incomplete. Here, we describe human monoclonal antibodies (mAbs) from a patient with a pandemic H1N1 virus infection in 2009. Two mAbs exhibited broad reactivity and inhibited NA enzyme activity of seasonal H1N1 viruses circulating before and after 2009, as well as viruses with avian or swine N1s. The mAbs provided robust protection from lethal challenge with human H1N1 and avian H5N1 viruses in mice, and both target an epitope on the lateral face of NA. In summary, we identified two broadly protective NA antibodies that share a novel epitope, inhibited NA activity, and provide protection against virus challenge in mice. Our work reaffirms that NA should be included as a target in future broadly protective or universal influenza virus vaccines.
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