New-onset dermatomyositis following SARS-CoV-2 infection and vaccination: a case-based review.


Journal

Rheumatology international
ISSN: 1437-160X
Titre abrégé: Rheumatol Int
Pays: Germany
ID NLM: 8206885

Informations de publication

Date de publication:
12 2022
Historique:
received: 06 05 2022
accepted: 22 07 2022
pubmed: 9 8 2022
medline: 12 10 2022
entrez: 8 8 2022
Statut: ppublish

Résumé

Dermatomyositis is a rare, type I interferon-driven autoimmune disease, which can affect muscle, skin and internal organs (especially the pulmonary system). In 2021, we have noted an increase in new-onset dermatomyositis compared to the years before the SARS-CoV-2 pandemic in our center. We present four cases of new-onset NXP2 and/or MDA5 positive dermatomyositis shortly after SARS-CoV-2 infection or vaccination. Three cases occurred within days after vaccination with Comirnaty and one case after SARS-CoV-2 infection. All patients required intensive immunosuppressive treatment. MDA5 antibodies could be detected in three patients and NXP2 antibodies were found in two patients (one patient was positive for both antibodies). In this case-based systematic review, we further analyze and discuss the literature on SARS-CoV-2 and associated dermatomyositis. In the literature, sixteen reports (with a total of seventeen patients) of new-onset dermatomyositis in association with a SARS-CoV-2 infection or vaccination were identified. Ten cases occurred after infection and seven after vaccination. All vaccination-associated cases were seen in mRNA vaccines. The reported antibodies included for instance MDA5, NXP2, Mi-2 and TIF1γ. The reviewed literature and our cases suggest that SARS-CoV-2 infection and vaccination may be considered as a potential trigger of interferon-pathway. Consequently, this might serve as a stimulus for the production of dermatomyositis-specific autoantibodies like MDA5 and NXP2 which are closely related to viral defense or viral RNA interaction supporting the concept of infection and vaccination associated dermatomyositis.

Identifiants

pubmed: 35939078
doi: 10.1007/s00296-022-05176-3
pii: 10.1007/s00296-022-05176-3
pmc: PMC9358381
doi:

Substances chimiques

Autoantibodies 0
Interferon Type I 0
RNA, Viral 0

Types de publication

Journal Article Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2267-2276

Informations de copyright

© 2022. The Author(s).

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Auteurs

Marie-Therese Holzer (MT)

III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. m.holzer@uke.de.
Department of Rheumatology and Immunology, Klinikum Bad Bramstedt, Bad Bramstedt, Germany. m.holzer@uke.de.

Martin Krusche (M)

III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Nikolas Ruffer (N)

III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Department of Rheumatology and Immunology, Klinikum Bad Bramstedt, Bad Bramstedt, Germany.

Heinrich Haberstock (H)

Department of Rheumatology and Immunology, Klinikum Bad Bramstedt, Bad Bramstedt, Germany.

Marlene Stephan (M)

Department of Rheumatology and Immunology, Klinikum Bad Bramstedt, Bad Bramstedt, Germany.

Tobias B Huber (TB)

III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Ina Kötter (I)

III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Department of Rheumatology and Immunology, Klinikum Bad Bramstedt, Bad Bramstedt, Germany.

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