Safety of the BNT162b2 mRNA COVID-19 vaccine in patients with familial Mediterranean fever.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
28 06 2022
Historique:
received: 12 12 2021
accepted: 22 02 2022
pubmed: 4 3 2022
medline: 1 7 2022
entrez: 3 3 2022
Statut: ppublish

Résumé

Evidence suggests a possible association between the COVID-19 vaccine and autoimmune disease flares or new onset of various autoinflammatory manifestations, such as pericarditis and myocarditis. The objective of this study was to assess the safety of an mRNA-based BNT162b2 anti-COVID-19 vaccine in individuals with FMF, a prototypic autoinflammatory disease. Patients participating in this study fulfilled the criteria for diagnosis of FMF, were older than 18 years and received at least one dose of the vaccine. Data on baseline characteristics, features of FMF, post-vaccination side effects, and disease flares were acquired using electronic medical files and telephone interviews. A total of 273 FMF patients were recruited for the study. >95% were vaccinated with two doses of the vaccine. The rates of local reactions following the first and second vaccine doses were 65.5% and 60%, respectively, and 26% and 50.4%, respectively, for systemic adverse events. These rates are lower than those reported for the general population from real-world and clinical trial settings. Postvaccination FMF activity remained stable in most patients. None of the patients reported an attack of pericarditis or myocarditis, considered the most serious vaccine-associated adverse events. Patients with a more active FMF disease and patients harboring the M694V mutation had a significantly higher rate of post-vaccination systemic side effects and attacks. The BNT162b2 mRNA COVID-19 vaccine is safe in patients with FMF. Our results support the administration of this vaccine to FMF patients according to guidelines applicable to the general population.

Identifiants

pubmed: 35238382
pii: 6541632
doi: 10.1093/rheumatology/keac131
pmc: PMC8903441
doi:

Substances chimiques

RNA, Messenger 0
BNT162 Vaccine N38TVC63NU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

SI129-SI135

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology.

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Auteurs

Liran Shechtman (L)

Department of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.

Karney Lahad (K)

Department of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.

Avi Livneh (A)

Department of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.
Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv.

Chagai Grossman (C)

Department of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.
Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv.

Amit Druyan (A)

Department of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.
Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv.

Eitan Giat (E)

Rheumatology Unit, Sheba Medical Center, Tel-Hashomer.

Merav Lidar (M)

Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv.
Rheumatology Unit, Sheba Medical Center, Tel-Hashomer.

Sarit Freund (S)

Faculty of Industrial Engineering and Management, Ruppin Academic Center.

Uri Manor (U)

Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv.
Department of Internal Medicine C, Sheba Medical Center, Tel-Hashomer.

Alon Pomerantz (A)

Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem.

Daniel Veroslavski (D)

Rappaport Faculty of Medicine, Technion University, Haifa.

Ilan Ben-Zvi (I)

Department of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.
Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv.
The Sheba Talpiot Medical Leadership Program, Tel-Hashomer, Israel.

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