Literature DB >> 21647771

[Autoinflammatory diseases as cause of wound healing defects].

R Löhrer1, R Eming, N Wolfrum, T Krieg, S A Eming.   

Abstract

Ulcerations of the skin and mucosal membranes are a common feature of autoinflammatory diseases. They can give raise to chronic wound healing defects and should be considered in the differential diagnosis of chronic skin ulcers. The increased activation of the innate immune system in the absence of an apparent provocation for inflammation is a hallmark of autoinflammatory diseases. Mutations and alterations of signaling pathways regulating the innate immune response to physical trauma/tissue damage result into an unrestrained activation of the inflammasome, which leads to increased activation of Interleukin-1. Uncontrolled recruitment and activation of myeloid effector cells within the wound site lead to the release of potent proteases that cause the degradation of structural components of the skin. The majority of these diseases respond well to immunosuppressive and immunomodulatory treatment regimes. Therapeutic resistance converts the acute inflammatory response into a chronic and non-resolving inflammatory process that leads to tissue degeneration. In this article we will focus on the review of those autoinflammatory diseases that often display ulcerative cutaneous and aphthous lesions including pyoderma gangrenosum, Behçet disease, PAPA syndrome and hyperimmunoglobulinemia D with periodic fever syndrome (HIDS). Furthermore, the article will be complemented by an overview of those inflammatory diseases that are associated with non-ulcerative cutaneous manifestations.

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Year:  2011        PMID: 21647771     DOI: 10.1007/s00105-010-2115-4

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  33 in total

1.  Strong association between plasma thrombomodulin and pathergy test in Behçet disease.

Authors:  S Menashi; B Tribout; C Dosquet; P Le Toumelin; J-C Piette; B Wechsler; M-C Boffa
Journal:  Ann Rheum Dis       Date:  2008-06       Impact factor: 19.103

2.  [Interleukin-1 cytokines, inflammasomes, NOD-signalosomes and autoinflammation].

Authors:  S D Gadola
Journal:  Z Rheumatol       Date:  2009-11       Impact factor: 1.372

Review 3.  Familial autoinflammatory diseases: genetics, pathogenesis and treatment.

Authors:  Silvia Stojanov; Daniel L Kastner
Journal:  Curr Opin Rheumatol       Date:  2005-09       Impact factor: 5.006

Review 4.  Pyoderma gangrenosum: a review and update on new therapies.

Authors:  Jeremiah Miller; Brad A Yentzer; Adele Clark; Joseph L Jorizzo; Steven R Feldman
Journal:  J Am Acad Dermatol       Date:  2010-04       Impact factor: 11.527

5.  Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. The International FMF Consortium.

Authors: 
Journal:  Cell       Date:  1997-08-22       Impact factor: 41.582

6.  [Adult-onset Still's disease, Schnitzler syndrome, and autoinflammatory syndromes in adulthood].

Authors:  P Lamprecht
Journal:  Z Rheumatol       Date:  2009-11       Impact factor: 1.372

7.  Corticosteroid sparing effect of low dose methotrexate treatment in adult Still's disease.

Authors:  B Fautrel; C Borget; S Rozenberg; O Meyer; X Le Loët; C Masson; A C Koeger; M F Kahn; P Bourgeois
Journal:  J Rheumatol       Date:  1999-02       Impact factor: 4.666

Review 8.  Autoinflammatory diseases: clinical and genetic advances.

Authors:  Sharifeh Farasat; Ivona Aksentijevich; Jorge R Toro
Journal:  Arch Dermatol       Date:  2008-03

9.  Complex aphthosis: a forme fruste of Behçet's syndrome?

Authors:  J L Jorizzo; R S Taylor; F C Schmalstieg; A R Solomon; J C Daniels; H E Rudloff; T Cavallo
Journal:  J Am Acad Dermatol       Date:  1985-07       Impact factor: 11.527

10.  Anti-interleukin-1 alpha autoantibodies in humans: characterization, isotype distribution, and receptor-binding inhibition--higher frequency in Schnitzler's syndrome (urticaria and macroglobulinemia).

Authors:  J H Saurat; J Schifferli; G Steiger; J M Dayer; L Didierjean
Journal:  J Allergy Clin Immunol       Date:  1991-08       Impact factor: 10.793

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  2 in total

Review 1.  Atypical severe combined immunodeficiency caused by a novel homozygous mutation in Rag1 gene in a girl who presented with pyoderma gangrenosum: a case report and literature review.

Authors:  Turkan Patiroglu; H Haluk Akar; Kimberly Gilmour; M Akif Ozdemir; Shahnaz Bibi; Frances Henriquez; Siobhan O Burns; Ekrem Unal
Journal:  J Clin Immunol       Date:  2014-08-08       Impact factor: 8.317

2.  Vaginal extrusion of a ventriculo-peritoneal shunt catheter in an adult.

Authors:  Christopher M Bonfield; Gregory M Weiner; Megan S Bradley; Johnathan A Engh
Journal:  J Neurosci Rural Pract       Date:  2015-01
  2 in total

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