Clinical significance of anti-Ro52 (TRIM21) antibodies in adult patients with connective tissue diseases.


Journal

European journal of internal medicine
ISSN: 1879-0828
Titre abrégé: Eur J Intern Med
Pays: Netherlands
ID NLM: 9003220

Informations de publication

Date de publication:
09 2021
Historique:
received: 13 01 2021
revised: 02 03 2021
accepted: 19 04 2021
pubmed: 12 5 2021
medline: 16 10 2021
entrez: 11 5 2021
Statut: ppublish

Résumé

Clinical significance of anti-Ro52 antibodies in connective tissue diseases (CTD) is controversial. Anti-Ro52 antibodies might be associated with a more severe CTD phenotype, especially interstitial lung disease (ILD). The aims of this study were to evaluate ILD prevalence and severity, the prevalence of micro- or macroangiopathy and CTD-associated cancers in CTD with anti-Ro52 antibodies. CTD patients with anti-Ro52 antibody screening by immunoblot at diagnosis were enrolled. Two groups were retrospectively formed according to the presence of anti-Ro52 antibodies with an unbiased 1:1 matching on CTD types. Unsupervised multiple correspondence analysis and hierarchical clustering analysis were used to aggregate anti-Ro52 positive patients in subgroups. 408 CTD patients were included. Anti-Ro52 antibodies were detected in 33 % of CTD patients. Anti-Ro52 antibodies were associated with ILD at CTD diagnosis (47.8% vs. 23.0%, OR 3.3 95% IC 1.4 to 8.0, p = 0.008), even after adjusting for the presence of anti-Ro60 antibodies, especially in patients with antisynthetase syndrome, primary Sjögren syndrome and systemic sclerosis. Micro- or macroangiopathy was more frequent in anti-Ro52 positive CTD patients (18.6% vs. 9.7%, p = 0.02) and CTD patients with anti-Ro52 antibodies experienced more frequent relapses and required more immunosuppressive drugs. Clusters 4 and 5 identified anti-Ro52 positive CTD patients with severe ILD and with clinical features of systemic sclerosis or antisynthetase syndrome respectively. We found that anti-Ro52 antibodies were independently associated with ILD in CTD patients irrespective of CTD type. Anti-Ro52 antibodies could be associated with severity and a more relapsing disease course in CTD patients.

Identifiants

pubmed: 33972152
pii: S0953-6205(21)00143-6
doi: 10.1016/j.ejim.2021.04.020
pii:
doi:

Substances chimiques

Autoantibodies 0
Ribonucleoproteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

45-52

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Auteurs

Paul Decker (P)

Department of Internal Medicine and Clinical Immunology, Regional Competence Center for Systemic and Autoimmune Rare Diseases, Nancy University Hospital, Lorraine University, Vandoeuvre-lès-Nancy, France. Electronic address: p.decker@chru-nancy.fr.

Thomas Moulinet (T)

Department of Internal Medicine and Clinical Immunology, Regional Competence Center for Systemic and Autoimmune Rare Diseases, Nancy University Hospital, Lorraine University, Vandoeuvre-lès-Nancy, France; UMR 7365, IMoPA, Lorraine University, CNRS, Nancy, France.

Benjamin Lopez (B)

Department of Immunology, Lille University Hospital, Lille 2 University, Lille, France.

Sylvain Dubucquoi (S)

Department of Immunology, Lille University Hospital, Lille 2 University, Lille, France.

Bernard Bonnotte (B)

Department of Internal Medicine and Clinical Immunology, Regional Competence Center for Systemic and Autoimmune Rare Diseases, Dijon University Hospital, Burgundy University, Dijon, France.

Daniela Lakomy (D)

Department of Immunology, Dijon University Hospital, Burgundy University, Dijon, France.

Sabine Revuz (S)

Department of Internal Medicine, Metz Private Hospital, Metz, France.

Amandine Luc (A)

Unity of Methodology, data management and statistic, Nancy University Hospital, Vandoeuvre-lès-Nancy, France.

Marcelo De Carvalho Bittencourt (MC)

Department of Immunology, Nancy University Hospital, Lorraine University, Vandoeuvre-lès-Nancy, France; UMR 7365, IMoPA, Lorraine University, CNRS, Nancy, France.

Eric Hachulla (E)

Department of Internal Medicine and Clinical Immunology, National Reference Center for Rare Systemic Autoimmune Diseases North and North-West of France, Claude Huriez Hospital, Lille University, Lille, France.

Roland Jaussaud (R)

Department of Internal Medicine and Clinical Immunology, Regional Competence Center for Systemic and Autoimmune Rare Diseases, Nancy University Hospital, Lorraine University, Vandoeuvre-lès-Nancy, France.

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Classifications MeSH