Literature DB >> 25639832

A missense mutation underlies defective SOCS4 function in a family with autoimmunity.

P Arts1, T S Plantinga2, J M van den Berg3, C Gilissen1, J A Veltman1,4, A S van Trotsenburg5, F L van de Veerdonk2, T W Kuijpers3, A Hoischen1, M G Netea2.   

Abstract

OBJECTIVE: The aim of this study was to determine the genetic and immunological defects underlying familial manifestations of an autoimmune disorder.
METHODS: Whole-exome sequencing was performed on the index patient with various manifestations of autoimmunity, including hypothyroidism, vitiligo and alopecia. Peripheral blood mononuclear cells and DNA of family members were used for functional and genetic testing of the candidate variants obtained by Sanger sequencing.
RESULTS: Exome sequencing identified 233 rare, coding and nonsynonymous variants in the index patient; five were highly conserved and affect genes that have a possible role in autoimmunity. Only a heterozygous missense mutation in the suppressor of cytokine signalling 4 gene (SOCS4) cosegregated with the autoimmune disorder in the family. SOCS4 is a known inhibitor of epidermal growth factor (EGF) receptor signalling, and functional studies demonstrated specific upregulation of EGF-dependent immune stimulation in affected family members.
CONCLUSION: We present a family with an autoimmune disorder, probably resulting from dysregulated immune responses due to mutations in SOCS4.
© 2015 The Association for the Publication of the Journal of Internal Medicine.

Entities:  

Keywords:  EGF; SOCS4; autoimmunity; exome sequencing; interleukin-6

Mesh:

Substances:

Year:  2015        PMID: 25639832     DOI: 10.1111/joim.12351

Source DB:  PubMed          Journal:  J Intern Med        ISSN: 0954-6820            Impact factor:   8.989


  2 in total

1.  Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies.

Authors:  Peer Arts; Annet Simons; Mofareh S AlZahrani; Elanur Yilmaz; Eman AlIdrissi; Koen J van Aerde; Njood Alenezi; Hamza A AlGhamdi; Hadeel A AlJubab; Abdulrahman A Al-Hussaini; Fahad AlManjomi; Alaa B Alsaad; Badr Alsaleem; Abdulrahman A Andijani; Ali Asery; Walid Ballourah; Chantal P Bleeker-Rovers; Marcel van Deuren; Michiel van der Flier; Erica H Gerkes; Christian Gilissen; Murad K Habazi; Jayne Y Hehir-Kwa; Stefanie S Henriet; Esther P Hoppenreijs; Sarah Hortillosa; Chantal H Kerkhofs; Riikka Keski-Filppula; Stefan H Lelieveld; Khurram Lone; Marius A MacKenzie; Arjen R Mensenkamp; Jukka Moilanen; Marcel Nelen; Jaap Ten Oever; Judith Potjewijd; Pieter van Paassen; Janneke H M Schuurs-Hoeijmakers; Anna Simon; Tomasz Stokowy; Maartje van de Vorst; Maaike Vreeburg; Anja Wagner; Gijs T J van Well; Dimitra Zafeiropoulou; Evelien Zonneveld-Huijssoon; Joris A Veltman; Wendy A G van Zelst-Stams; Eissa A Faqeih; Frank L van de Veerdonk; Mihai G Netea; Alexander Hoischen
Journal:  Genome Med       Date:  2019-06-17       Impact factor: 11.117

2.  Progressive multifocal leukoencephalopathy in an immunocompetent patient.

Authors:  Nicolien M van der Kolk; Peer Arts; Ingeborg W M van Uden; Alexander Hoischen; Frank L van de Veerdonk; Mihai G Netea; Brigit A de Jong
Journal:  Ann Clin Transl Neurol       Date:  2016-01-08       Impact factor: 4.511

  2 in total

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