Combining multi-antigenic immunodot with indirect immunofluorescence on HEp-2 cells improves the diagnosis of systemic sclerosis.


Journal

Clinical immunology (Orlando, Fla.)
ISSN: 1521-7035
Titre abrégé: Clin Immunol
Pays: United States
ID NLM: 100883537

Informations de publication

Date de publication:
08 2021
Historique:
received: 11 02 2021
revised: 03 06 2021
accepted: 04 06 2021
pubmed: 11 6 2021
medline: 18 9 2021
entrez: 10 6 2021
Statut: ppublish

Résumé

Systemic sclerosis (SSc) is associated, in nearly all patients, with autoantibodies (Ab). Accordingly, and in order to identify major (anti-CEN A/B and anti-Topo I) but also minor Abs, the usefulness of combining indirect immunofluorescence (IIF) on HEp-2 cells with an 11 multi-antigenic SSc immunodot was explored. 1689 samples tested at the request of clinicians, were evaluated retrospectively. The positivity rate was 28.8% and the diagnosis of SSc was supported for 232 samples. Two groups of Abs were considered: group 1, Abs (anti-CENP A/B, anti-Topo I) present at elevated levels in SSc patients; group 2, Abs for which the Ab specificity (odds ratio and/or positive predictive value) was improved by using IIF on HEp-2 cells (RNA-Polymerase III, fibrillarin, Th/T0, PM-Scl). Altogether, this study highlights the utility of combining IIF on HEp-2 cells with the SSc immunodot as the first line of an SSc Abs detection/SSc diagnostic strategy.

Identifiants

pubmed: 34111525
pii: S1521-6616(21)00111-X
doi: 10.1016/j.clim.2021.108774
pii:
doi:

Substances chimiques

Autoantibodies 0
Autoantigens 0
CENPA protein, human 0
CENPB protein, human 0
Centromere Protein A 0
Centromere Protein B 0
DNA Topoisomerases, Type I EC 5.99.1.2
TOP1 protein, human EC 5.99.1.2

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108774

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Chloé Bost (C)

Immunology laboratory, Institut Fédératif de Biologie, Toulouse University Hospital Center, France; INSERM U1043, CNRS UMR 5282, Toulouse III University, Center for Pathophysiology Toulouse Purpan, Toulouse, France. Electronic address: bost.c@chu-toulouse.fr.

Françoise Fortenfant (F)

Immunology laboratory, Institut Fédératif de Biologie, Toulouse University Hospital Center, France. Electronic address: fortenfant.f@chu-toulouse.fr.

Antoine Blancher (A)

Immunology laboratory, Institut Fédératif de Biologie, Toulouse University Hospital Center, France; INSERM U1043, CNRS UMR 5282, Toulouse III University, Center for Pathophysiology Toulouse Purpan, Toulouse, France. Electronic address: blancher.a@chu-toulouse.fr.

Grégory Pugnet (G)

Department of Internal Medicine, Toulouse University Hospital Center, France; Clinical Investigation Center 1436, CHU Toulouse, Toulouse, France. Electronic address: pugnet.g@chu-toulouse.fr.

Yves Renaudineau (Y)

Immunology laboratory, Institut Fédératif de Biologie, Toulouse University Hospital Center, France; INSERM U1043, CNRS UMR 5282, Toulouse III University, Center for Pathophysiology Toulouse Purpan, Toulouse, France. Electronic address: renaudineau.y@chu-toulouse.fr.

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Classifications MeSH