Anti-SARS-CoV-2 vaccination in adolescent and adult patients with juvenile-onset systemic lupus erythematosus: tolerability and impact on disease activity.


Journal

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

Informations de publication

Date de publication:
01 09 2023
Historique:
received: 20 10 2022
accepted: 13 01 2023
medline: 4 9 2023
pubmed: 27 1 2023
entrez: 26 1 2023
Statut: ppublish

Résumé

JSLE has a severe presentation and a remitting course. Patients with JSLE carry an increased vulnerability to infections, which also act as triggers of disease flare. Thus, vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an important tool in JSLE. The objective of this study is to evaluate the tolerability and the safety of anti-SARS-CoV-2 vaccination, including the booster, in a monocentric cohort of JSLE patients. Clinical records of JSLE patients who received at least one dose of any anti-SARS-CoV-2 vaccine were retrospectively reviewed. Data about disease activity, treatment, anti-SARS-CoV-2 vaccination and COVID-19 infection were collected. Sixty-five JSLE patients received at least one dose of anti-SARS-CoV-2 vaccination, while 46 patients completed the schedule with the booster. The rate of mild-moderate adverse events was 66%, mainly comprising fever, fatigue, arthromyalgias and pain at injection site. The rate of adverse events after the booster was similar to that registered after the first two doses. No significant changes after SARS-CoV-2 vaccination in BILAG and SLEDAI were observed. Disease flare rate (mainly LN) after immunization was 10.8%. Flares occurred predominantly in patients with moderate disease activity before immunization; accordingly, SLEDAI ≥4 identified patients at risk of flare while Lupus Low Disease Activity State (LLDAS) plays a protective role against post-vaccination flare. This study confirms that anti-SARS-CoV-2 vaccination in JSLE is well tolerated; a strict clinical monitoring and a thoughtful choice of vaccination timing should be devoted to patients not in LLDAS due to the risk of post-vaccine flare.

Identifiants

pubmed: 36702464
pii: 7005195
doi: 10.1093/rheumatology/kead047
doi:

Substances chimiques

COVID-19 Vaccines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3146-3150

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Cecilia Beatrice Chighizola (CB)

Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
Pediatric Rheumatology Unit, ASST Pini-CTO, Milan, Italy.

Ilaria Suardi (I)

Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
Clinical Rheumatology Unit, ASST Pini-CTO, Milan, Italy.

Giulia Carrea (G)

Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
Clinical Rheumatology Unit, ASST Pini-CTO, Milan, Italy.

Lorenza Argolini (L)

Clinical Rheumatology Unit, ASST Pini-CTO, Milan, Italy.

Maurizio Gattinara (M)

Pediatric Rheumatology Unit, ASST Pini-CTO, Milan, Italy.

Achille Marino (A)

Pediatric Rheumatology Unit, ASST Pini-CTO, Milan, Italy.

Irene Pontikaki (I)

Pediatric Rheumatology Unit, ASST Pini-CTO, Milan, Italy.

Roberto Caporali (R)

Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
Clinical Rheumatology Unit, ASST Pini-CTO, Milan, Italy.

Maria Gerosa (M)

Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
Clinical Rheumatology Unit, ASST Pini-CTO, Milan, Italy.

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