Declining Levels of Neutralizing Antibodies to SARS-CoV-2 Omicron Variants Are Enhanced by Hybrid Immunity and Original/Omicron Bivalent Vaccination.

Omicron SARS-Cov-2 breakthrough infection hybrid immunity neutralizing antibody vaccine variant

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
22 May 2024
Historique:
received: 09 04 2024
revised: 09 05 2024
accepted: 15 05 2024
medline: 27 6 2024
pubmed: 27 6 2024
entrez: 27 6 2024
Statut: epublish

Résumé

We determined neutralizing antibody levels to the ancestral Wuhan SARS-CoV-2 strain and three Omicron variants, namely BA.5, XBB.1.5, and EG.5, in a heavily vaccinated cohort of 178 adults 15-19 months after the initial vaccine series and prospectively after 4 months. Although all participants had detectable neutralizing antibodies to Wuhan, the proportion with detectable neutralizing antibodies to the Omicron variants was decreased, and the levels were lower. Individuals with hybrid immunity at the baseline visit and those receiving the Original/Omicron bivalent vaccine between the two sampling times demonstrated increased neutralizing antibodies to all strains. Both a higher baseline neutralizing antibody titer to Omicron BA.5 and hybrid immunity were associated with protection against a breakthrough SARS-CoV-2 infection during a 4-month period of follow up during the Omicron BA.5 wave. Neither were associated with protection from a breakthrough infection at 10 months follow up. Receipt of an Original/Omicron BA.4/5 vaccine was associated with protection from a breakthrough infection at both 4 and 10 months follow up. This work demonstrates neutralizing antibody escape with the emerging Omicron variants and supports the use of additional vaccine doses with components that match circulating SARS-CoV-2 variants. A threshold value for neutralizing antibodies for protection against reinfection cannot be determined.

Identifiants

pubmed: 38932293
pii: vaccines12060564
doi: 10.3390/vaccines12060564
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Public Health Agency of Canada, Canadian Immunity Task Force
ID : 087-VS
Organisme : University Health Network Foundation
ID : Speck Family COVID-19 Research

Auteurs

Sharon Walmsley (S)

Division of Infectious Diseases, University Health Network, Toronto, ON M5G 2C4, Canada.
Department of Medicine, University of Toronto, Toronto, ON M5S 1A1, Canada.

Majid Nabipoor (M)

Biostatistics Department, University Health Network, Toronto, ON M5G 2C4, Canada.

Freda Qi (F)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health, Toronto, ON M5G 1X5, Canada.

Leif Erik Lovblom (LE)

Biostatistics Department, University Health Network, Toronto, ON M5G 2C4, Canada.

Rizani Ravindran (R)

Division of Infectious Diseases, University Health Network, Toronto, ON M5G 2C4, Canada.

Karen Colwill (K)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health, Toronto, ON M5G 1X5, Canada.

Roya Monica Dayam (RM)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health, Toronto, ON M5G 1X5, Canada.

Tulunay R Tursun (TR)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health, Toronto, ON M5G 1X5, Canada.

Amanda Silva (A)

DATA Team, University Health Network, Toronto, ON M5G 2C4, Canada.

Anne-Claude Gingras (AC)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health, Toronto, ON M5G 1X5, Canada.
Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A1, Canada.

Classifications MeSH