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SARS-CoV-2 mRNA vaccine design enabled by prototype pathogen preparedness

Authors :
Corbett, Kizzmekia S.
Edwards, Darin K.
Leist, Sarah R.
Abiona, Olubukola M.
Boyoglu-Barnum, Seyhan
Gillespie, Rebecca A.
Himansu, Sunny
Schäfer, Alexandra
Ziwawo, Cynthia T.
DiPiazza, Anthony T.
Dinnon, Kenneth H.
Elbashir, Sayda M.
Shaw, Christine A.
Woods, Angela
Fritch, Ethan J.
Martinez, David R.
Bock, Kevin W.
Minai, Mahnaz
Nagata, Bianca M.
Hutchinson, Geoffrey B.
Wu, Kai
Henry, Carole
Bahl, Kapil
Garcia-Dominguez, Dario
Ma, LingZhi
Renzi, Isabella
Kong, Wing-Pui
Schmidt, Stephen D.
Wang, Lingshu
Zhang, Yi
Phung, Emily
Chang, Lauren A.
Loomis, Rebecca J.
Altaras, Nedim Emil
Narayanan, Elisabeth
Metkar, Mihir
Presnyak, Vlad
Liu, Cuiping
Louder, Mark K.
Shi, Wei
Leung, Kwanyee
Yang, Eun Sung
West, Ande
Gully, Kendra L.
Stevens, Laura J.
Wang, Nianshuang
Wrapp, Daniel
Doria-Rose, Nicole A.
Stewart-Jones, Guillaume
Bennett, Hamilton
Alvarado, Gabriela S.
Nason, Martha C.
Ruckwardt, Tracy J.
McLellan, Jason S.
Denison, Mark R.
Chappell, James D.
Moore, Ian N.
Morabito, Kaitlyn M.
Mascola, John R.
Baric, Ralph S.
Carfi, Andrea
Graham, Barney S.
Source :
Nature; October 2020, Vol. 586 Issue: 7830 p567-571, 5p
Publication Year :
2020

Abstract

A vaccine for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is needed to control the coronavirus disease 2019 (COVID-19) global pandemic. Structural studies have led to the development of mutations that stabilize Betacoronavirusspike proteins in the prefusion state, improving their expression and increasing immunogenicity1. This principle has been applied to design mRNA-1273, an mRNA vaccine that encodes a SARS-CoV-2 spike protein that is stabilized in the prefusion conformation. Here we show that mRNA-1273 induces potent neutralizing antibody responses to both wild-type (D614) and D614G mutant2SARS-CoV-2 as well as CD8+T cell responses, and protects against SARS-CoV-2 infection in the lungs and noses of mice without evidence of immunopathology. mRNA-1273 is currently in a phase III trial to evaluate its efficacy.

Details

Language :
English
ISSN :
00280836 and 14764687
Volume :
586
Issue :
7830
Database :
Supplemental Index
Journal :
Nature
Publication Type :
Periodical
Accession number :
ejs54406072
Full Text :
https://doi.org/10.1038/s41586-020-2622-0