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Broad protection against clade 1 sarbecoviruses after a single immunization with cocktail spike-protein-nanoparticle vaccine

Nature Communications. 2023-07; 
Peter J. Halfmann; Kathryn Loeffler; Augustine Duffy; Makoto Kuroda; Jie E. Yang; Elizabeth R. Wright; Yoshihiro Kawaoka; Ravi S. Kane
Products/Services Used Details Operation
PCR Cloning and Subcloning dimer was cloned into pET-28b between the Ndel and XhoI restriction sites, and an AviTag was inserted between residues 14 and 15 of the second monomer by GenScript Biotech Corporation (Piscataway, NJ) 14 , 29 . The MS2-AviTag plasmid was co-transformed with a plasmid containing BirA biotin-protein ligase into BL21( Get A Quote

摘要

The 2002 SARS outbreak, the 2019 emergence of COVID-19, and the continuing evolution of immune-evading SARS-CoV-2 variants together highlight the need for a broadly protective vaccine against ACE2-utilizing sarbecoviruses. While updated variant-matched formulations are a step in the right direction, protection needs to extend beyond SARS-CoV-2 and its variants to include SARS-like viruses. Here, we introduce bivalent and trivalent vaccine formulations using our spike protein nanoparticle platform that completely protect female hamsters against BA.5 and XBB.1 challenges with no detectable virus in the lungs. The trivalent cocktails elicit highly neutralizing responses against all tested Omicron variants and the ... More

关键词

Protein vaccines, Nanobiotechnology, SARS-CoV-2, SARS virus