Durability of Immune Responses After Boosting in Ad26.COV2.S-Primed Healthcare Workers.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
08 02 2023
Historique:
received: 15 04 2022
pubmed: 21 6 2022
medline: 11 2 2023
entrez: 20 6 2022
Statut: ppublish

Résumé

The emergence of SARS-CoV-2 variants raised questions regarding the durability of immune responses after homologous or heterologous boosters after Ad26.COV2.S-priming. We found that SARS-CoV-2-specific binding antibodies, neutralizing antibodies, and T cells are detectable 5 months after boosting, although waning of antibodies and limited cross-reactivity with Omicron BA.1 was observed.

Identifiants

pubmed: 35723273
pii: 6611568
doi: 10.1093/cid/ciac495
pmc: PMC9384313
doi:

Substances chimiques

Ad26COVS1 JT2NS6183B
Antibodies, Neutralizing 0
Antibodies, Viral 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e533-e536

Subventions

Organisme : NCEZID CDC HHS
ID : U01 CK000632
Pays : United States

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Déclaration de conflit d'intérêts

Potential conflicts of interest. L. G. V. reports research grants from U Needle, MyLife Technologies, and Bavarian Nordic, all outside of the submitted work; consulting fees from Emergent for expert meeting travel vaccines; participation on a scientific advisory board for Geosentinel; and serving as committee member for the National Board Guideline Development Travel Medicine. A. G. reports participation on a data and safety monitoring board (DSMB) IDSCOVA (Establishing the tolerability, safety and immunogenicity of intradermal delivery of mRNA SARS-CoV-2 vaccine in healthy adults) study on intradermal COVID vaccinations and serving as member of national advisory board on coronavirus disease vaccinations for immunocompromised patients. A. L. W. H. reports support for the present research from the Dutch Research Council (ZonMw) to their organization. D. F. P. reports participation on the DSMB of the COBRA-KAI trial (COVID-19 vaccination in patients with reduced B-cell and T-cell immunity: response after vaccination in a kaleidoscopic group of hematologic patients: what's the impact?). V. A. S. H. D. reports research funding outside of the submitted work from ZonMw and EU Horizon 2020, consulting fees for an advisory board meeting from GSK, and honoraria for lectures from Pharming, Takeda. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Auteurs

Roos S G Sablerolles (RSG)

Department of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.
Department of Hospital Pharmacy, Erasmus Medical Center, Rotterdam, The Netherlands.

Wim J R Rietdijk (WJR)

Department of Hospital Pharmacy, Erasmus Medical Center, Rotterdam, The Netherlands.

Abraham Goorhuis (A)

Center of Tropical Medicine and Travel Medicine, Department of Infectious Diseases, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
Infection & Immunity, Amsterdam Public Health, University of Amsterdam, Amsterdam, The Netherlands.

Douwe F Postma (DF)

Department of Internal Medicine and Infectious Diseases, University Medical Center Groningen, Groningen, The Netherlands.

Leo G Visser (LG)

Department of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.

Katharina S Schmitz (KS)

Department of Viroscience, Erasmus Medical Center, Rotterdam, The Netherlands.

Daryl Geers (D)

Department of Viroscience, Erasmus Medical Center, Rotterdam, The Netherlands.

Susanne Bogers (S)

Department of Viroscience, Erasmus Medical Center, Rotterdam, The Netherlands.

Eva van Haren (E)

Department of Hospital Pharmacy, Erasmus Medical Center, Rotterdam, The Netherlands.

Marion P G Koopmans (MPG)

Department of Viroscience, Erasmus Medical Center, Rotterdam, The Netherlands.

Virgil A S H Dalm (VASH)

Department of Internal Medicine, Division of Allergy & Clinical Immunology and Department of Immunology, Erasmus Medical Center, Rotterdam, The Netherlands.

Neeltje A Kootstra (NA)

Department of Experimental Immunology, Amsterdam University Medical Centers, Amsterdam Infection and Immunity Institute, University of Amsterdam, Amsterdam, The Netherlands.

Anke L W Huckriede (ALW)

Department of Medical Microbiology and Infection Prevention, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Renate Akkerman (R)

Department of Medical Microbiology and Infection Prevention, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Martin Beukema (M)

Department of Medical Microbiology and Infection Prevention, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Melvin Lafeber (M)

Department of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.

Debbie van Baarle (D)

Department of Medical Microbiology and Infection Prevention, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Center for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.

Rory D de Vries (RD)

Department of Viroscience, Erasmus Medical Center, Rotterdam, The Netherlands.

P Hugo M van der Kuy (PHM)

Department of Hospital Pharmacy, Erasmus Medical Center, Rotterdam, The Netherlands.

Corine H GeurtsvanKessel (CH)

Department of Viroscience, Erasmus Medical Center, Rotterdam, The Netherlands.

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