Effect of Systemic Lupus Erythematosus and Immunosuppressive Agents on COVID-19 Vaccination Antibody Response.


Journal

Arthritis care & research
ISSN: 2151-4658
Titre abrégé: Arthritis Care Res (Hoboken)
Pays: United States
ID NLM: 101518086

Informations de publication

Date de publication:
09 2023
Historique:
revised: 03 01 2023
received: 05 09 2022
accepted: 26 01 2023
pmc-release: 01 09 2024
medline: 31 8 2023
pubmed: 31 1 2023
entrez: 30 1 2023
Statut: ppublish

Résumé

The risk of COVID-19 infection is increased in patients with systemic lupus erythematosus (SLE) versus those without SLE. Some immunosuppressive medications increase COVID-19 infection and decrease the efficacy of vaccination. Consensus documents have suggested management strategies for handling immunosuppressive medications to increase vaccine efficacy, but the benefit of such strategies has not been proven. The current study was undertaken to determine the effect of immunosuppressive drugs on vaccine response in SLE. We collected information on COVID-19 infection, vaccination history, and COVID-19 antibodies in the Hopkins Lupus Cohort. A cohort of health care workers was used for comparison. Outcome measures included SARS-CoV-2 antibody IgG levels after vaccination over time in both cohorts and effect of immunosuppressive medications on postvaccination IgG levels in SLE patients. The analysis was based on 365 observations from 334 different patients in the SLE cohort, and 2,235 observations from 1,887 different health care workers. SLE patients taking immunosuppressive medications had lower vaccine IgG levels than SLE patients who were not; but both groups had lower levels than health care workers. Holding mycophenolate for 1 week after vaccination increased postvaccine IgG levels significantly without leading to clinical flares. In multiple variable models, mycophenolate mofetil, tacrolimus, and belimumab all significantly reduced antibody response to vaccination. SLE patients, regardless of background immunosuppressive therapy, had lower vaccine IgG levels than health care workers. Mycophenolate, tacrolimus, and belimumab significantly reduced IgG response to vaccination. Holding mycophenolate for 1 week improved vaccine efficacy, providing clinical benefit on vaccine response without leading to clinical flares.

Identifiants

pubmed: 36714913
doi: 10.1002/acr.25094
pmc: PMC10387122
mid: NIHMS1869558
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0
Immunoglobulin G 0
Immunosuppressive Agents 0
Tacrolimus WM0HAQ4WNM

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1878-1885

Subventions

Organisme : NIAID NIH HHS
ID : T32 AI007291
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR069572
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI141580
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023 The Authors. Arthritis Care & Research published by Wiley Periodicals LLC on behalf of American College of Rheumatology.

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Auteurs

Michelle Petri (M)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Daniel Joyce (D)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Kristin Haag (K)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Andrea Fava (A)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Daniel W Goldman (DW)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Diana Zhong (D)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Shaoming Xiao (S)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Aaron Milstone (A)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Laurence S Magder (LS)

University of Baltimore School of Medicine, Baltimore, Maryland.

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Classifications MeSH