Breadth of SARS-CoV-2 neutralization and protection induced by a nanoparticle vaccine

纳米颗粒疫苗对SARS-CoV-2的中和广度和保护作用

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作者:Dapeng Li ,David R Martinez ,Alexandra Schäfer ,Haiyan Chen ,Maggie Barr ,Laura L Sutherland ,Esther Lee ,Robert Parks ,Dieter Mielke ,Whitney Edwards ,Amanda Newman ,Kevin W Bock ,Mahnaz Minai ,Bianca M Nagata ,Matthew Gagne ,Daniel C Douek ,C Todd DeMarco ,Thomas N Denny ,Thomas H Oguin 3rd ,Alecia Brown ,Wes Rountree ,Yunfei Wang ,Katayoun Mansouri ,Robert J Edwards ,Guido Ferrari ,Gregory D Sempowski ,Amanda Eaton ,Juanjie Tang ,Derek W Cain ,Sampa Santra ,Norbert Pardi ,Drew Weissman ,Mark A Tomai ,Christopher B Fox ,Ian N Moore ,Hanne Andersen ,Mark G Lewis ,Hana Golding ,Robert Seder ,Surender Khurana ,Ralph S Baric ,David C Montefiori ,Kevin O Saunders ,Barton F Haynes

Abstract

Coronavirus vaccines that are highly effective against current and anticipated SARS-CoV-2 variants are needed to control COVID-19. We previously reported a receptor-binding domain (RBD)-sortase A-conjugated ferritin nanoparticle (scNP) vaccine that induced neutralizing antibodies against SARS-CoV-2 and pre-emergent sarbecoviruses and protected non-human primates (NHPs) from SARS-CoV-2 WA-1 infection. Here, we find the RBD-scNP induced neutralizing antibodies in NHPs against pseudoviruses of SARS-CoV and SARS-CoV-2 variants including 614G, Beta, Delta, Omicron BA.1, BA.2, BA.2.12.1, and BA.4/BA.5, and a designed variant with escape mutations, PMS20. Adjuvant studies demonstrate variant neutralization titers are highest with 3M-052-aqueous formulation (AF). Immunization twice with RBD-scNPs protect NHPs from SARS-CoV-2 WA-1, Beta, and Delta variant challenge, and protect mice from challenges of SARS-CoV-2 Beta variant and two other heterologous sarbecoviruses. These results demonstrate the ability of RBD-scNPs to induce broad neutralization of SARS-CoV-2 variants and to protect animals from multiple different SARS-related viruses. Such a vaccine could provide broad immunity to SARS-CoV-2 variants.

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