A review of the immunogenicity and safety of booster doses of omicron variant-containing mRNA-1273 COVID-19 vaccines in adults and children.

COVID-19 SARS-CoV-2 booster mRNA-1273 omicron vaccine variant of concern

Journal

Expert review of vaccines
ISSN: 1744-8395
Titre abrégé: Expert Rev Vaccines
Pays: England
ID NLM: 101155475

Informations de publication

Date de publication:
05 Sep 2024
Historique:
medline: 5 9 2024
pubmed: 5 9 2024
entrez: 5 9 2024
Statut: aheadofprint

Résumé

Vaccination against SARS-CoV-2 is an integral pillar of the public health approach to COVID-19. With the emergence of variants of concern that increase transmissibility and escape from vaccine- or infection-induced protection, vaccines have been developed to more closely match the newly circulating SARS-CoV-2 strains to improve protection. The safety and immunogenicity of multiple authorized messenger RNA (mRNA)-based COVID-19 vaccines targeting the omicron sublineage (BA.1, BA.4/BA.5, and XBB.1.5) have been demonstrated in several clinical trials among adults and children. This review will comprehensively detail the available evidence (published through December 2023) from ongoing clinical trials on omicron variant-containing mRNA-1273 vaccines administered as additional doses in previously vaccinated target demographics. Across three clinical trials, omicron variant-containing mRNA-1273 vaccines induced immune responses to vaccine-matched omicron strains as well as ancestral SARS-CoV-2, with a safety and reactogenicity profile comparable to the original mRNA-1273 vaccine. Combined with pivotal data demonstrating the safety, efficacy, and effectiveness of the original mRNA-1273 vaccine, these findings support the use of variant-containing mRNA-1273 vaccines and provide confidence that expeditious development of updated vaccines using this established mRNA platform can maintain protection against COVID-19.

Identifiants

pubmed: 39234779
doi: 10.1080/14760584.2024.2397026
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Frances Priddy (F)

Moderna, Inc, Cambridge, MA, USA.

Spyros Chalkias (S)

Moderna, Inc, Cambridge, MA, USA.

Brandon Essink (B)

Meridian Clinical Research, Omaha, NE, USA.

Jordan Whatley (J)

Meridian Clinical Research, Baton Rouge, LA, USA.

Adam Brosz (A)

Meridian Clinical Research, Savannah, GA, USA.

Ivan T Lee (IT)

Moderna, Inc, Cambridge, MA, USA.

Jing Feng (J)

Moderna, Inc, Cambridge, MA, USA.

LaRee Tracy (L)

Moderna, Inc, Cambridge, MA, USA.

Weiping Deng (W)

Moderna, Inc, Cambridge, MA, USA.

Wen Zhou (W)

Moderna, Inc, Cambridge, MA, USA.

Honghong Zhou (H)

Moderna, Inc, Cambridge, MA, USA.

Avika Dixit (A)

Moderna, Inc, Cambridge, MA, USA.

Sabine Snyder-Ghamloush (S)

Moderna, Inc, Cambridge, MA, USA.

Bethany Girard (B)

Moderna, Inc, Cambridge, MA, USA.

Elizabeth de Windt (E)

Moderna, Inc, Cambridge, MA, USA.

Anne Yeakey (A)

Moderna, Inc, Cambridge, MA, USA.

Jacqueline Miller (J)

Moderna, Inc, Cambridge, MA, USA.

Rituparna Das (R)

Moderna, Inc, Cambridge, MA, USA.

Barbara J Kuter (BJ)

Moderna, Inc, Cambridge, MA, USA.

Classifications MeSH