Back to Search Start Over

Bivalent and Monovalent SARS-CoV-2 Variant Vaccine Boosters Improve coverage of the known Antigenic Landscape: Results of the COVID-19 Variant Immunologic Landscape (COVAIL) Trial

Authors :
Angela Branche
Nadine Rouphael
David Diemert
Ann Falsey
Cecilia Losada
Lindsey (R) Baden
Sharon Frey
Jennifer Whitaker
Susan Little
Evan Anderson
Emmanuel Walter
Richard Novak
Richard Rupp
Lisa Jackson
Tara Babu
Angelica Kottkamp
Annie Luetkemeyer
Lilly Immergluck
Rachel Presti
Martin Backer
Patricia Winokur
Siham Mahgoub
Paul Goepfert
Dahlene Fusco
Elissa Malkin
Jeff Bethony
Edward Walsh
Daniel Graciaa
Hady Samaha
Amy Sherman
Stephen Walsh
Getahun Abate
Zacharoula Oikonomopoulou
Hana El Sahly
Thomas Martin
Satoshi Kamidani
Michael Smith
Benjamin Ladner
Laura Porterfield
Maya Dunstan
Anna Wald
Tamia Davis
Robert Atmar
Mark Mulligan
Kirsten Lyke
Christine Posavad
Megan Meagher
David Stephens
Kathleen Neuzil
Kuleni Abebe
Heather Hill
Jim Albert
Kalyani Telu
Jinjian Mu
Teri Lewis
Lisa Giebeig
Amanda Eaton
Antonia Netzl
Sam Wilks
Sina Tureli
Mamodikoe Makhene
Sonja Crandon
David Montefiori
Mat Makowski
Derek Smith
Seema Nayak
Paul Roberts
John Beigel
Publication Year :
2023
Publisher :
Research Square Platform LLC, 2023.

Abstract

Vaccine protection against COVID-19 wanes over time and has been impacted by the emergence of new variants with increasing escape of neutralization. The COVID-19 Variant Immunologic Landscape (COVAIL) randomized clinical trial (clinicaltrials.gov NCT 05289037) compares the breadth, magnitude and durability of antibody responses induced by a second COVID-19 vaccine boost with mRNA (Moderna mRNA-1273 and Pfizer-BioNTech BNT162b2), or adjuvanted recombinant protein (Sanofi CoV2 preS DTM-AS03) monovalent or bivalent vaccine candidates targeting ancestral and variant SARS-CoV-2 spike antigens (Beta, Delta and Omicron BA.1). We found that boosting with a variant strain is not associated with loss in neutralization against the ancestral strain. However, while variant vaccines compared to the prototype/wildtype vaccines demonstrated higher neutralizing activity against Omicron BA.1 and BA.4/5 subvariants for up to 3 months after vaccination, neutralizing activity was lower for more recent Omicron subvariants. Our study, incorporating both antigenic distances and serologic landscapes, can provide a framework for objectively guiding decisions for future vaccine updates.

Details

Database :
OpenAIRE
Accession number :
edsair.doi...........3b575ca893eb1aa83c279fb0e1184ce3