Humoral Response of Patients With Autoimmune Rheumatic Disease to BNT162b2 Vaccine: A Retrospective Comparative Study.

anti-sars-cov-2 vaccine autoimmune rheumatic disease disease modifying antirheumatic drug humoral immune response rituximab

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
Apr 2022
Historique:
accepted: 29 04 2022
entrez: 2 6 2022
pubmed: 3 6 2022
medline: 3 6 2022
Statut: epublish

Résumé

Objective The effectiveness and safety of SARS-CoV-2 vaccines in patients with autoimmune rheumatic diseases (ARDs) treated with immunomodulators remain uncertain. Therefore, this study aimed to evaluate whether the humoral immune response to the BNT162b2 vaccine differs between patients without and with ARDs treated with immunomodulators. Methods We retrospectively reviewed 3208 electronic medical records from the database of the Hamad Medical Corporation (HMC) outpatient rheumatology clinics to capture patients with ARDs and control patients without autoimmune inflammatory diseases. All patients who were SARS-CoV-2 infection-naïve, had received two doses of BNT162b2 vaccination, and had been serologically tested using Elecsys® anti-SARS-CoV-2 S immunoassays (Roche Holdings AG, Basel, Switzerland), were included in the analysis. Patients with ARD were classified into six subgroups according to the received ARD immunomodulators: methotrexate monotherapy (MTXM), a combination of conventional synthetic disease-modifying antirheumatic drugs (Cs-DMARDs), tumor necrosis factor inhibitor (TNF-i), rituximab, interleukin-6 inhibitor (IL6-i), and Janus kinase inhibitor (JAK-i). Samples with an anti-SARS-CoV-2 S titer of <0.8 and <132 binding antibody unit (BAU)/mL were defined as negative and poor seroconversion, respectively. The overall mean of anti-SARS-CoV-2 S titer and its level at <0.8 and <132 were compared between the six subgroups of patients with ARD and the controls by performing an unpaired 

Identifiants

pubmed: 35651432
doi: 10.7759/cureus.24585
pmc: PMC9138718
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e24585

Informations de copyright

Copyright © 2022, Alsaed et al.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Omar Alsaed (O)

Medicine Department, Rheumatology Division, Hamad Medical Corporation, Doha, QAT.

Samar Al Emadi (S)

Medicine Department, Rheumatology Division, Hamad Medical Corporation, Doha, QAT.

Eman Satti (E)

Medicine Department, Rheumatology Division, Hamad Medical Corporation, Doha, QAT.

Bassam Muthanna (B)

Medicine Department, Rheumatology Division, Hamad Medical Corporation, Doha, QAT.

Safna Farsana Akkam Veettil (SF)

Medicine Department, Rheumatology Division, Hamad Medical Corporation, Doha, QAT.

Hadeel Ashour (H)

Medicine Department, Rheumatology Division, Hamad Medical Corporation, Doha, QAT.

Prem Chandra (P)

Medical Research Center, Hamad Medical Corporation, Doha, QAT.

Einas A Alkuwari (EA)

Department of Laboratory Medicine and Pathology, Hamad Medical Corporation, Doha, QAT.

Peter Coyle (P)

Department of Laboratory Medicine and Pathology, Hamad Medical Corporation, Doha, QAT.

Classifications MeSH