Association of anti-SARS-COV-2 vaccine with increased incidence of myositis-related anti-RNA-synthetases auto-antibodies.
COVID19
Interstitial lung disease
Myositis
Myositis specific antibodies
SARS-CoV-2 vaccines
Journal
Journal of translational autoimmunity
ISSN: 2589-9090
Titre abrégé: J Transl Autoimmun
Pays: Netherlands
ID NLM: 101759413
Informations de publication
Date de publication:
2022
2022
Historique:
received:
25
04
2022
revised:
08
06
2022
accepted:
18
06
2022
entrez:
5
7
2022
pubmed:
6
7
2022
medline:
6
7
2022
Statut:
epublish
Résumé
SARS-CoV-2 is a RNA virus that associates with heterogeneous clinical manifestations and complications. Auto-antibodies are identified in approximately 50% of hospitalized COVID-19 patients. To determine the global incidence of myositis-related auto-antibodies (non Jo1-RNA synthetases: anti-PL7, anti-PL12, anti-EJ, anti-OJ and RNA-sensor: anti-MDA5) in our laboratory during COVID-19 pandemics, and to describe the clinical and laboratory features of these patients. A retrospective study was performed from 2015 to 2021 in a cohort of 444 patients with suspected inflammatory myopathy. The incidence of positive results for the MSA was expressed as absolute value per year for the reference population. Immunoblot analysis, indirect immunofluorescence and HLA typing of 36 patients with positivity for MSAs were collected and analyzed. We observed MSA positive in 28 patients in 2020 and 36 patients in 2021, representing a mean increase of 6-fold respect to previous years since 2015 (range, 0 to 19). In 2020, the most common antibody detected was anti-MDA5 (68%). In contrast, in 2021 the most common antibodies were anti-PL7 and/or anti-PL12 (69%). All patients in 2021 with positive anti-synthetases were fully vaccinated, 4 had previous documented infection, with median time from vaccine to MSA positivity of 5 months. Eight out of 36 patients (22%) reported clinical onset after SARS-CoV-2 vaccination and 6 out of 36 (17%) presented clinical and/or radiological worsening after SARS-CoV-2 vaccination. All patients presented with a known human leukocyte antigen (HLA)-DRB1* allele associated with ASS. The most prevalent alleles identified were DRB1*03:01, DRB1*04, DRB1*11:01, corresponding to 70% (16/23) of our cohort. Our preliminary data show an increased incidence of anti-synthetase antibodies during COVID-19 pandemic and SARS-CoV-2 vaccination associated to HLA DRB1* risk allele. Differential profiles of MSA specificities were observed: mainly against RNA-sensors in 2020 and against RNA-synthetases in 2021. Further studies are needed to support the association between SARS-CoV-2 infection and/or vaccination and the occurrence of this autoimmune syndrome.
Identifiants
pubmed: 35789569
doi: 10.1016/j.jtauto.2022.100160
pii: S2589-9090(22)00021-1
pmc: PMC9242685
doi:
Types de publication
Journal Article
Langues
eng
Pagination
100160Informations de copyright
© 2022 Published by Elsevier B.V.
Déclaration de conflit d'intérêts
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Références
Autoimmun Rev. 2014 Jan;13(1):31-9
pubmed: 24001753
Front Neurol. 2019 May 08;10:438
pubmed: 31139133
Int Immunopharmacol. 2021 Oct;99:107970
pubmed: 34280851
Rheumatology (Oxford). 2017 Jun 1;56(6):999-1007
pubmed: 28339994
J Autoimmun. 2019 Mar;98:24-32
pubmed: 30459097
Scand J Infect Dis. 2013 Jul;45(7):537-42
pubmed: 23427875
QJM. 2021 Oct 7;114(6):424-425
pubmed: 33647971
Nat Rev Rheumatol. 2018 Apr 20;14(5):290-302
pubmed: 29674612
Chest. 2010 Dec;138(6):1464-74
pubmed: 21138882
J Exp Med. 2002 Sep 16;196(6):781-91
pubmed: 12235211
Joint Bone Spine. 2017 May;84(3):251-253
pubmed: 28017820
QJM. 2021 Nov 13;114(9):659-660
pubmed: 34109386
Lancet Rheumatol. 2021 Nov;3(11):e747-e749
pubmed: 34585145
Front Immunol. 2021 Dec 20;12:791348
pubmed: 34987516
Medicine (Baltimore). 2006 Mar;85(2):111-127
pubmed: 16609350
BMJ Case Rep. 2021 Apr 28;14(4):
pubmed: 33910791
Hum Genomics. 2019 Jan 8;13(1):2
pubmed: 30621780
Clin Immunol. 2021 Mar;224:108665
pubmed: 33429060
J Autoimmun. 2022 Jan;126:102780
pubmed: 34923432
Nat Rev Rheumatol. 2009 Nov;5(11):648-52
pubmed: 19865091
Autoimmun Rev. 2010 Mar;9(5):A330-4
pubmed: 19906360
Cleve Clin J Med. 2021 Dec 2;88(12):648-650
pubmed: 34857596
Neurology. 2013 Apr 2;80(14):1315-21
pubmed: 23486871
Immunology. 2022 Apr;165(4):386-401
pubmed: 34957554
Ann Rheum Dis. 2020 Oct;79(10):1383-1386
pubmed: 32444414
Clin Exp Immunol. 1998 Nov;114(2):161-5
pubmed: 9822271
Rheumatology (Oxford). 2015 Jan;54(1):50-63
pubmed: 25065005
Lancet Neurol. 2018 Sep;17(9):816-828
pubmed: 30129477
J Bras Pneumol. 2011 Jan-Feb;37(1):100-9
pubmed: 21390438
EBioMedicine. 2019 Apr;42:76-85
pubmed: 30952617
Mod Rheumatol. 2016;26(3):403-9
pubmed: 26344678