Neutralising antibody responses to SARS-CoV-2 omicron among elderly nursing home residents following a booster dose of BNT162b2 vaccine: A community-based, prospective, longitudinal cohort study.

Antibodies Elderly individuals Omicron SARS-CoV-2 Vaccine

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 05 04 2022
revised: 01 07 2022
accepted: 04 07 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 28 7 2022
Statut: epublish

Résumé

The protective immunity against omicron following a BNT162b2 Pfizer booster dose among elderly individuals (ie, those aged >65 years) is not well characterised. In a community-based, prospective, longitudinal cohort study taking place in France in which 75 residents from three nursing homes were enrolled, we selected 38 residents who had received a two-dose regimen of mRNA vaccine and a booster dose of Pfizer BNT162b2 vaccine. We excluded individuals that did not receive three vaccine doses or did not have available sera samples. We measured anti-S IgG antibodies and neutralisation capacity in sera taken 56 (28-68) and 55 (48-64) days (median (range)) after the 2 Among the 38 elderly individuals recruited to the cohort study between November 23 This study shows that elderly individuals who received three vaccine doses elicit neutralising antibodies against the omicron BA.1 variant of SARS-CoV-2. Elderly individuals who had also been previously infected showed higher neutralising activity compared with naive individuals. Yet, breakthrough infections with omicron occurred. Individuals with breakthrough infections had significantly lower neutralising titers compared to individuals without breakthrough infection. Thus, a fourth dose of vaccine may be useful in the elderly population to increase the level of neutralising antibodies and compensate for waning immunity. Institut Pasteur, Fondation pour la Recherche Médicale (FRM), European Health Emergency Preparedness and Response Authority (HERA), Agence nationale de recherches sur le sida et les hépatites virales - Maladies Infectieuses Emergentes (ANRS-MIE), Agence nationale de la recherche (ANR), Assistance Publique des Hôpitaux de Paris (AP-HP) and Fondation de France.

Sections du résumé

Background UNASSIGNED
The protective immunity against omicron following a BNT162b2 Pfizer booster dose among elderly individuals (ie, those aged >65 years) is not well characterised.
Methods UNASSIGNED
In a community-based, prospective, longitudinal cohort study taking place in France in which 75 residents from three nursing homes were enrolled, we selected 38 residents who had received a two-dose regimen of mRNA vaccine and a booster dose of Pfizer BNT162b2 vaccine. We excluded individuals that did not receive three vaccine doses or did not have available sera samples. We measured anti-S IgG antibodies and neutralisation capacity in sera taken 56 (28-68) and 55 (48-64) days (median (range)) after the 2
Findings UNASSIGNED
Among the 38 elderly individuals recruited to the cohort study between November 23
Interpretation UNASSIGNED
This study shows that elderly individuals who received three vaccine doses elicit neutralising antibodies against the omicron BA.1 variant of SARS-CoV-2. Elderly individuals who had also been previously infected showed higher neutralising activity compared with naive individuals. Yet, breakthrough infections with omicron occurred. Individuals with breakthrough infections had significantly lower neutralising titers compared to individuals without breakthrough infection. Thus, a fourth dose of vaccine may be useful in the elderly population to increase the level of neutralising antibodies and compensate for waning immunity.
Funding UNASSIGNED
Institut Pasteur, Fondation pour la Recherche Médicale (FRM), European Health Emergency Preparedness and Response Authority (HERA), Agence nationale de recherches sur le sida et les hépatites virales - Maladies Infectieuses Emergentes (ANRS-MIE), Agence nationale de la recherche (ANR), Assistance Publique des Hôpitaux de Paris (AP-HP) and Fondation de France.

Identifiants

pubmed: 35891947
doi: 10.1016/j.eclinm.2022.101576
pii: S2589-5370(22)00306-6
pmc: PMC9307278
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101576

Informations de copyright

© 2022 The Authors.

Déclaration de conflit d'intérêts

SvdW is a member of the Data Safety Monitoring Board of the DISCOVERY trial and the EU-solidact trial, and an associate editor within the Eurosurveillance journal. MW and SP declare a pending patent (US 63/057.471), SvdW declares issued patents (EP1697507, EP1694829, PCT/EP2020055939, US16/809.717 and WO20211176099), and a provisional patent (US63003855). All the other authors declare no competing interests.

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Auteurs

Timothée Bruel (T)

Virus & Immunity Unit, Institut Pasteur, Université Paris Cité, CNRS UMR 3569, Paris, France.
Vaccine Research Institute, Créteil, France.

Laurie Pinaud (L)

Emerging Diseases Epidemiology Unit, Institut Pasteur, Université Paris Cité, Paris, France.

Laura Tondeur (L)

Emerging Diseases Epidemiology Unit, Institut Pasteur, Université Paris Cité, Paris, France.

Delphine Planas (D)

Virus & Immunity Unit, Institut Pasteur, Université Paris Cité, CNRS UMR 3569, Paris, France.
Vaccine Research Institute, Créteil, France.

Isabelle Staropoli (I)

Virus & Immunity Unit, Institut Pasteur, Université Paris Cité, CNRS UMR 3569, Paris, France.

Françoise Porrot (F)

Virus & Immunity Unit, Institut Pasteur, Université Paris Cité, CNRS UMR 3569, Paris, France.

Florence Guivel-Benhassine (F)

Virus & Immunity Unit, Institut Pasteur, Université Paris Cité, CNRS UMR 3569, Paris, France.

Mikaël Attia (M)

Molecular Genetics of RNA Viruses Unit, Institut Pasteur, Université Paris Cité, Paris, France.

Stéphane Pelleau (S)

Infectious Disease Epidemiology and Analytics Unit, Institut Pasteur, Université Paris Cité, Paris, France.

Tom Woudenberg (T)

Infectious Disease Epidemiology and Analytics Unit, Institut Pasteur, Université Paris Cité, Paris, France.

Cécile Duru (C)

Hôpital de Crépy-en-Valois, Crépy-en-Valois, France.

Aymar Davy Koffi (AD)

Hôpital de Crépy-en-Valois, Crépy-en-Valois, France.

Sandrine Castelain (S)

Laboratoire de virologie, CHU Amiens, AGIR UR4294, UPJV, Amiens, France.

Sandrine Fernandes-Pellerin (S)

Centre for Translational Science, Institut Pasteur, Paris, France.

Nathalie Jolly (N)

Centre for Translational Science, Institut Pasteur, Paris, France.

Louise Perrin De Facci (LP)

Clinical Investigation and access to bioresources (ICAReB) platform, Centre for Translational Science, Institut Pasteur, Paris, France.

Emmanuel Roux (E)

Clinical Investigation and access to bioresources (ICAReB) platform, Centre for Translational Science, Institut Pasteur, Paris, France.

Marie-Noëlle Ungeheuer (MN)

Clinical Investigation and access to bioresources (ICAReB) platform, Centre for Translational Science, Institut Pasteur, Paris, France.

Sylvie Van Der Werf (S)

Molecular Genetics of RNA Viruses Unit, Institut Pasteur, Université Paris Cité, Paris, France.

Michael White (M)

Infectious Disease Epidemiology and Analytics Unit, Institut Pasteur, Université Paris Cité, Paris, France.

Olivier Schwartz (O)

Virus & Immunity Unit, Institut Pasteur, Université Paris Cité, CNRS UMR 3569, Paris, France.
Vaccine Research Institute, Créteil, France.

Arnaud Fontanet (A)

Emerging Diseases Epidemiology Unit, Institut Pasteur, Université Paris Cité, Paris, France.
Conservatoire National des Arts et Métiers, PACRI Unit, Paris, France.

Classifications MeSH