单克隆抗体
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
中和
2019年冠状病毒病(COVID-19)
病毒学
抗体
接种疫苗
2019-20冠状病毒爆发
冠状病毒感染
免疫学
医学
生物
疾病
内科学
爆发
传染病(医学专业)
作者
Jimin Lee,James Brett Case,Rashmi Ravichandran,Daniel Asarnow,M. Alejandra Tortorici,Jack T. Brown,Shilpa Sanapala,Lauren Carter,David A. Baker,Michael S Diamond,David Veesler
标识
DOI:10.1101/2024.08.08.606885
摘要
The continued evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has compromised neutralizing antibody responses elicited by prior infection or vaccination and abolished the utility of most monoclonal antibody therapeutics. We previously described a computationally-designed, homotrimeric miniprotein inhibitor, designated TRI2-2, that protects mice against pre-Omicron SARS-CoV-2 variants. Here, we show that TRI2-2 exhibits pan neutralization of variants that evolved during the 4.5 years since the emergence of SARS-CoV-2 and protects mice against BQ.1.1, XBB.1.5 and BA.2.86 challenge when administered post-exposure by an intranasal route. The resistance of TRI2-2 to viral escape and its direct delivery to the upper airways rationalize a path toward clinical advancement.
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