Circulation autoantibodies against C-terminus of NuMA in patients with Behçet's disease.

C-NuMA antigen epitope site autoantibody nuclear protein

Journal

Central-European journal of immunology
ISSN: 1426-3912
Titre abrégé: Cent Eur J Immunol
Pays: Poland
ID NLM: 9702239

Informations de publication

Date de publication:
2020
Historique:
received: 04 07 2017
accepted: 08 09 2017
entrez: 20 5 2020
pubmed: 20 5 2020
medline: 20 5 2020
Statut: ppublish

Résumé

Circulating autoantibodies have a close association with autoimmune diseases, which may be seen even in healthy individuals. These are also considered as promising source of new biomarkers in various autoimmune diseases. However, their profile is not completely understood till now. Here, we evaluated autoantibodies against nuclear mitotic apparatus protein located at the carboxy terminus (C-NuMA)in blood circulation of Han Chinese patients, using different technical approaches to discover pathological reaction leading to Behçet's disease (BD). In the first step, the recombinant human carboxy-terminal region of NuMA peptide (C-NuMA) was over-expressed and purified. In the second step, the indirect immunofluorescence method was used with patients' sera, and commercial anti-NuMA antibody was used to determine the NuMA as a potential autoantigen. Results were confirmed at cell level by western blots, indicating that two of ten patients with Behçet's disease could react with the recombinant C-NuMA,and the presence of antibodies were further verified by immunoprecipitation technique. Finally, the corresponding immunoassay (ELISA) was developed and optimized with specific recombinant C-NuMA as an in vitro method to test the confirmed patients with Behçet's disease. Our findings demonstrated that C-terminus of NuMA is an immune target of Behçet's disease in Han Chinese patients.

Identifiants

pubmed: 32425685
doi: 10.5114/ceji.2020.94710
pii: 94710
pmc: PMC7226561
doi:

Types de publication

Journal Article

Langues

eng

Pagination

86-92

Informations de copyright

Copyright © 2020 Termedia.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Muhammad Hussain (M)

112 Lab, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, China.

Fuxin Ma (F)

112 Lab, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, China.

Peng Chen (P)

112 Lab, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, China.

Yaping Tian (Y)

Department of Clinical Biochemistry, Chinese PLA General Hospital, Beijing, China.

Hongwu DU (H)

112 Lab, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, China.

Classifications MeSH