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Anti-MDA5 dermatomyositis after COVID-19 vaccination: a case-based review

Anti-MDA5 dermatomyositis after COVID-19 vaccination: a case-based review

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9166182

Anti-MDA5 dermatomyositis after COVID-19 vaccination: a case-based review

About this item

Full title

Anti-MDA5 dermatomyositis after COVID-19 vaccination: a case-based review

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

Journal title

Rheumatology international, 2022-09, Vol.42 (9), p.1629-1641

Language

English

Formats

Publication information

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

More information

Scope and Contents

Contents

Anti-MDA5 (Melanoma differentiation-associated protein 5) myositis is a rare subtype of dermatomyositis (DM) characterized by distinct ulcerative, erythematous cutaneous lesions and a high risk of rapidly progressive interstitial lung disease (RP-ILD). It has been shown that SARS-CoV-2 (COVID-19) replicates rapidly in lung and skin epithelial cells, which is sensed by the cytosolic RNA-sensor MDA5. MDA5 then triggers type 1 interferon (IFN) production, and thus downstream inflammatory mediators (EMBO J 40(15):e107826, 2021); (J Virol, 2021,
https://doi.org/10.1128/JVI.00862-21
); (Cell Rep 34(2):108628, 2021); (Sci Rep 11(1):13638, 2021); (Trends Microbiol 27(1):75–85, 2019). It has also been shown that MDA5 is triggered by the mRNA COVID-19 vaccine with resultant activated dendritic cells (Nat Rev Immunol 21(4):195–197, 2021). Our literature review identified one reported case of MDA5-DM from the COVID-19 vaccin...

Alternative Titles

Full title

Anti-MDA5 dermatomyositis after COVID-19 vaccination: a case-based review

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9166182

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9166182

Other Identifiers

ISSN

1437-160X,0172-8172

E-ISSN

1437-160X

DOI

10.1007/s00296-022-05149-6

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