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
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
101576Informations 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.
Références
Lancet Healthy Longev. 2021 Nov;2(11):e685-e687
pubmed: 34580665
Cell. 2022 Feb 3;185(3):467-484.e15
pubmed: 35081335
Nature. 2022 Apr;604(7906):553-556
pubmed: 35240676
Lancet Respir Med. 2021 Nov;9(11):e104-e105
pubmed: 34687656
N Engl J Med. 2022 Mar 17;386(11):1088-1091
pubmed: 35081298
Eur J Immunol. 2021 Jan;51(1):180-190
pubmed: 33259646
Nat Med. 2021 May;27(5):917-924
pubmed: 33772244
N Engl J Med. 2022 Feb 17;386(7):698-700
pubmed: 35021005
Lancet. 2022 Feb 19;399(10326):715-717
pubmed: 35065005
Eur J Immunol. 2022 May;52(5):816-824
pubmed: 35312186
Lancet Reg Health Eur. 2022 Jun;17:100385
pubmed: 35469147
N Engl J Med. 2022 Apr 28;386(17):1603-1614
pubmed: 35417631
EMBO J. 2020 Dec 1;39(23):e106267
pubmed: 33051876
Nature. 2021 Aug;596(7872):417-422
pubmed: 34192737
Ann Rheum Dis. 2022 May;81(5):720-728
pubmed: 35022159
Nature. 2022 Feb;602(7898):664-670
pubmed: 35016195
N Engl J Med. 2022 May 5;386(18):1712-1720
pubmed: 35381126
Nature. 2022 Feb;602(7898):671-675
pubmed: 35016199
Nature. 2022 Feb;602(7898):654-656
pubmed: 35016196
Nature. 2022 Feb;602(7898):682-688
pubmed: 35016197
Lancet Infect Dis. 2022 Apr;22(4):445-446
pubmed: 35240040
Nat Med. 2022 Mar;28(3):496-503
pubmed: 35090165
N Engl J Med. 2022 Apr 7;386(14):1377-1380
pubmed: 35297591
Sci Transl Med. 2020 Sep 2;12(559):
pubmed: 32817357
J Infect Dis. 2021 Sep 17;224(6):983-988
pubmed: 33693749
Nature. 2022 Feb;602(7898):657-663
pubmed: 35016194
Lancet Microbe. 2021 Feb;2(2):e60-e69
pubmed: 33521709
Cell. 2022 Feb 3;185(3):457-466.e4
pubmed: 34995482
Immunity. 2020 Sep 15;53(3):487-495
pubmed: 32853545
PLoS One. 2022 Apr 29;17(4):e0266958
pubmed: 35486622
Nature. 2022 Feb;602(7898):676-681
pubmed: 35016198