Literature DB >> 18264745

Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED.

D Moraes-Vasconcelos1, B T Costa-Carvalho, T R Torgerson, H D Ochs.   

Abstract

BACKGROUND: Several primary immune deficiency disorders are associated with autoimmunity and malignancy, suggesting a state of immune dysregulation. The concept of immune dysregulation as a direct cause of autoimmunity in primary immune deficiency disorders (PIDDs) has been strengthened by the recent discovery of distinct clinical entities linked to single-gene defects resulting in multiple autoimmune phenomena including immune dysregulation, polyendocrinopathy, enteropathy and X-linked (IPEX) syndrome, and autoimmune polyendocrinopathy, candidiasis and ectodermal dystrophy (APECED) syndrome.
CONCLUSION: Reviewing recent advances in our understanding of the small subgroup of PIDD patients with defined causes for autoimmunity may lead to the development of more effective treatment strategies for idiopathic human autoimmune diseases.

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Year:  2008        PMID: 18264745     DOI: 10.1007/s10875-008-9176-5

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  78 in total

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Authors:  L Perroni; F Faravelli; R Cusano; F Forzano; P De Cassan; C Baldo; F Dagna Bricarelli
Journal:  Prenat Diagn       Date:  2006-05       Impact factor: 3.050

Review 2.  A central role for central tolerance.

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5.  Successful use of the new immune-suppressor sirolimus in IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome).

Authors:  Lutz Bindl; Troy Torgerson; Lucia Perroni; Nelly Youssef; Hans D Ochs; Olivier Goulet; Frank M Ruemmele
Journal:  J Pediatr       Date:  2005-08       Impact factor: 4.406

6.  Positional cloning of the APECED gene.

Authors:  K Nagamine; P Peterson; H S Scott; J Kudoh; S Minoshima; M Heino; K J Krohn; M D Lalioti; P E Mullis; S E Antonarakis; K Kawasaki; S Asakawa; F Ito; N Shimizu
Journal:  Nat Genet       Date:  1997-12       Impact factor: 38.330

Review 7.  The genetic background of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy and its autoimmune disease components.

Authors:  Arndt Vogel; Christian P Strassburg; Petra Obermayer-Straub; Georg Brabant; Michael P Manns
Journal:  J Mol Med (Berl)       Date:  2002-02-05       Impact factor: 4.599

Review 8.  Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome.

Authors:  R S Wildin; S Smyk-Pearson; A H Filipovich
Journal:  J Med Genet       Date:  2002-08       Impact factor: 6.318

9.  Autoimmune polyendocrinopathy--candidosis--ectodermal dystrophy (APECED): autosomal recessive inheritance.

Authors:  P Ahonen
Journal:  Clin Genet       Date:  1985-06       Impact factor: 4.438

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Authors:  O Ekwall; H Hedstrand; L Grimelius; J Haavik; J Perheentupa; J Gustafsson; E Husebye; O Kämpe; F Rorsman
Journal:  Lancet       Date:  1998-07-25       Impact factor: 79.321

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6.  Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome.

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Journal:  J Allergy Clin Immunol       Date:  2013-03-25       Impact factor: 10.793

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8.  Clinical experience in T cell deficient patients.

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Review 9.  Rheumatologic manifestations of primary immunodeficiency diseases.

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10.  Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes.

Authors:  Oscar Rubio-Cabezas; Jayne A L Minton; Richard Caswell; Julian P Shield; Dorothee Deiss; Zdenek Sumnik; Amely Cayssials; Mathias Herr; Anja Loew; Vaughan Lewis; Sian Ellard; Andrew T Hattersley
Journal:  Diabetes Care       Date:  2008-10-17       Impact factor: 17.152

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