Literature DB >> 29317407

A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease.

Florence A Aeschlimann1, Ezgi D Batu2, Scott W Canna3, Ellen Go4, Ahmet Gül5, Patrycja Hoffmann6, Helen L Leavis7, Seza Ozen2, Daniella M Schwartz8, Deborah L Stone6, Annet van Royen-Kerkof9, Daniel L Kastner6, Ivona Aksentijevich6, Ronald M Laxer1,10.   

Abstract

OBJECTIVES: The association between mutations in TNFAIP3, encoding the NF-kB regulatory protein A20, and a new autoinflammatory disease has recently been recognised. This study aims at describing the clinical phenotypes and disease course of patients with A20 haploinsufficiency (HA20).
METHODS: Data for all cases from the initial publication, and additional cases identified through collaborations since, were collected using standardised data collection forms.
RESULTS: A total of 16 patients (13 female) from seven families with a genetic diagnosis of HA20 were included. The disease commonly manifested in early childhood (range: first week of life to 29 years of age). The main clinical symptoms were recurrent oral, genital and/or gastrointestinal ulcers (16/16), musculoskeletal (9/16) and gastrointestinal complaints (9/16), cutaneous lesions (8/16), episodic fever (7/16), and recurrent infections (7/16). Clinical phenotypes varied considerably, even within families. Relapsing-remitting disease course was most common, and one patient died. Laboratory abnormalities included elevated acute-phase reactants and fluctuating presence of various autoantibodies such as antinuclear antibodies (4/10 patients tested) and anti-dsDNA (2/5). Tissue biopsy of different sites revealed non-specific chronic inflammation (6/12 patients tested), findings consistent with class V lupus nephritis in one patient, and pustules and normal results in two patients each. All patients were treated: 4/16 received colchicine and 12/16 various immunosuppressive agents. Cytokine inhibitors effectively suppressed systemic inflammation in 7/9 patients.
CONCLUSIONS: Early-onset recurrent oral, genital and/or gastrointestinal ulcers are the hallmark feature of HA20. Frequency and intensity of other clinical manifestations varied highly. Treatment regimens should be based on disease severity, and cytokine inhibitors are often required to control relapses. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  autoinflammatory disease; pediatric rheumatology; ulcers

Mesh:

Substances:

Year:  2018        PMID: 29317407     DOI: 10.1136/annrheumdis-2017-212403

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  62 in total

1.  Type I interferon signature predicts response to JAK inhibition in haploinsufficiency of A20.

Authors:  Daniella Muallem Schwartz; Sarah A Blackstone; Natalia Sampaio-Moura; Sofia Rosenzweig; Aarohan M Burma; Deborah Stone; Patrycja Hoffmann; Anne Jones; Tina Romeo; Karyl S Barron; Meryl A Waldman; Ivona Aksentijevich; Daniel L Kastner; Joshua D Milner; Amanda K Ombrello
Journal:  Ann Rheum Dis       Date:  2019-11-25       Impact factor: 19.103

Review 2.  Diagnostic/classification criteria in pediatric Behçet's disease.

Authors:  Ezgi Deniz Batu
Journal:  Rheumatol Int       Date:  2018-11-14       Impact factor: 2.631

Review 3.  Moving towards a systems-based classification of innate immune-mediated diseases.

Authors:  Sinisa Savic; Emily A Caseley; Michael F McDermott
Journal:  Nat Rev Rheumatol       Date:  2020-02-27       Impact factor: 20.543

Review 4.  Autoinflammatory Disease-Associated Vasculitis/Vasculopathy.

Authors:  Mansour Alghamdi
Journal:  Curr Rheumatol Rep       Date:  2018-11-17       Impact factor: 4.592

Review 5.  A20: A multifunctional tool for regulating immunity and preventing disease.

Authors:  Barbara A Malynn; Averil Ma
Journal:  Cell Immunol       Date:  2019-04-05       Impact factor: 4.868

Review 6.  Advances and highlights in primary immunodeficiencies in 2017.

Authors:  Javier Chinen; Morton J Cowan
Journal:  J Allergy Clin Immunol       Date:  2018-08-29       Impact factor: 10.793

Review 7.  Monogenic systemic lupus erythematosus: insights in pathophysiology.

Authors:  Ezgi Deniz Batu
Journal:  Rheumatol Int       Date:  2018-05-15       Impact factor: 2.631

Review 8.  A20 at the Crossroads of Cell Death, Inflammation, and Autoimmunity.

Authors:  Arne Martens; Geert van Loo
Journal:  Cold Spring Harb Perspect Biol       Date:  2020-01-02       Impact factor: 10.005

9.  Clinical characteristics and genetic analysis of A20 haploinsufficiency.

Authors:  Dan Zhang; Gaixiu Su; Zhixuan Zhou; Jianming Lai
Journal:  Pediatr Rheumatol Online J       Date:  2021-05-24       Impact factor: 3.054

Review 10.  The Ubiquitin System and A20: Implications in Health and Disease.

Authors:  E C Mooney; S E Sahingur
Journal:  J Dent Res       Date:  2020-08-27       Impact factor: 6.116

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