抗体
噬菌体展示
流式细胞术
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
糖蛋白
单链
病毒学
免疫学
中和
2019年冠状病毒病(COVID-19)
生物
医学
分子生物学
疾病
病理
传染病(医学专业)
作者
Peng Shan-shan,Syed Hamad Ali Shah,Shengsheng Mei,Eu Gene Vong,Yi Sun,Jin-biao Zhan
标识
DOI:10.1016/j.intimp.2023.111020
摘要
As SARS-CoV-2 variants continue spreading globally, the discovery of broad spectrum therapeutically active antibodies with retaining good protective activity is a global priority. It was reported that infection with SARS-CoV-2 could cause acute lung injury (ALI) in clinical investigations. Therefore, we discovered that anti-RBD scFv is effective against SARS-CoV-2-induced ALI. To begin, we utilized the receptor binding domain (RBD) of spike glycoprotein as a target to produce single-chain antibodies (scFvs) through an intensive phage display technology. The binding affinity and inhibitory effect of the scFvs were evaluated via ELISA and flow cytometry. Moreover, anti-RBD scFv No.35 significantly prevented ALI caused by LPS and SARS-CoV-2 spike RBD protein in mouse model. Thus, the anti-RBD scFv will aid the development of potential antibody treatments and reduce the inflammatory response of SARS-CoV-2.
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