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Comprehensive review of autoantibodies in patients with hyper-IgM syndrome

Authors :
Zakera Shums
Mehdi Trifa
Imen Ben-Mustapha
Qubo Chen
Christopher Chang
Marco Carbone
Gary L. Norman
Francesca Bernuzzi
Mohamed-Ridha Barbouche
Federica Malinverno
M. Eric Gershwin
Nourhen Agrebi
Haiyan Zhang
Pietro Invernizzi
Barbouche, M
Chen, Q
Carbone, M
Ben-Mustapha, I
Shums, Z
Trifa, M
Malinverno, F
Bernuzzi, F
Zhang, H
Agrebi, N
Norman, G
Chang, C
Gershwin, M
Invernizzi, P
Source :
Cellular & Molecular Immunology. 15:610-617
Publication Year :
2018
Publisher :
Springer Science and Business Media LLC, 2018.

Abstract

Hyper-immunoglobulin M syndrome is an X-linked primary immunodeficiency disease caused by mutations in the CD40 ligand gene. The CD40 ligand has been recently highlighted as playing a key role in the pathogenesis of primary biliary cholangitis. In the present study, we assessed an extensive set of serum autoantibodies in a series of well-defined patients with hyper-immunoglobulin M syndrome. Serum, liver-related and liver-not-related autoantibodies IgG, IgM and IgA were tested by ELISA and standard indirect immunofluorescence in HEp-2 cells in 13 Tunisian patients (8 males and 5 females, aged 1–12 years) with hyper-immunoglobulin M syndrome during 1995–2012 and, as controls, 21 age- and gender-matched blood donors. The level of IgM antibody against MIT3 was significantly higher in patients than in controls (35.8 vs 10.7, P=0.002). Half of the hyperimmunoglobulin M syndrome patients were found to be anti-MIT3 IgM positive vs none of the controls (P

Details

ISSN :
20420226 and 16727681
Volume :
15
Database :
OpenAIRE
Journal :
Cellular & Molecular Immunology
Accession number :
edsair.doi.dedup.....d1e8f5172f6140b780b94caf3ca01e3b
Full Text :
https://doi.org/10.1038/cmi.2017.140