免疫原
病毒学
病毒
免疫
甲型流感病毒
医学
中和
疫苗效力
抗体
免疫学
生物
微生物学
接种疫苗
单克隆抗体
作者
Jaehyun Hwang,Inyoung Jang,Eun Young Bae,Jaeseok Choi,Jeong Hwan Kim,Sang Beum Lee,Jong Hyun Kim,J. Lee,Hyonchol Jang,Hyoung Tae Kim,Jong-Woo Lim,Minjoo Yeom,Eun‐Hee Jang,Seong‐Eun Kim,Hyoung Hwa Jeong,Jung Ho Kim,Seung‐Yong Seong,Daesub Song,Woonsung Na
标识
DOI:10.1016/j.biopha.2024.116781
摘要
Influenza A virus causes numerous deaths and infections worldwide annually. Therefore, we have considered nanobodies as a potential treatment for patients with severe cases of influenza. We developed a nanobody that was expected to have protective efficacy against the A/California/04/2009 (CA/04; pandemic 2009 flu strain) and evaluated its therapeutic efficacy against CA/04 in mice experiments. This nanobody was derived from the immunization of the alpaca, and the inactivated CA/04 virus was used as an immunogen. We successfully generated a nanobody library through bio-panning, phage ELISA, and Bio-layer interferometry. Moreover, we confirmed that administering nanobodies after lethal doses of CA/04 reduced viral replication in the lungs and influenza-induced clinical signs in mice. These research findings will help to develop nanobodies as viral therapeutics for CA/04 and other infectious viruses.
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