Literature DB >> 28629746

Mechanisms of genotype-phenotype correlation in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency.

Daniel Petersheim1, Michel J Massaad1, Saetbyul Lee1, Alessia Scarselli2, Caterina Cancrini2, Kunihiko Moriya3, Yoji Sasahara3, Arjan C Lankester4, Morna Dorsey5, Daniela Di Giovanni6, Liliana Bezrodnik6, Hidenori Ohnishi7, Ryuta Nishikomori8, Kay Tanita9, Hirokazu Kanegane9, Tomohiro Morio9, Erwin W Gelfand10, Ashish Jain11, Elizabeth Secord12, Capucine Picard13, Jean-Laurent Casanova14, Michael H Albert15, Troy R Torgerson16, Raif S Geha17.   

Abstract

BACKGROUND: Autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency (AD EDA-ID) is caused by heterozygous point mutations at or close to serine 32 and serine 36 or N-terminal truncations in IκBα that impair its phosphorylation and degradation and thus activation of the canonical nuclear factor κ light chain enhancer of activated B cells (NF-κB) pathway. The outcome of hematopoietic stem cell transplantation is poor in patients with AD EDA-ID despite achievement of chimerism. Mice heterozygous for the serine 32I mutation in IκBα have impaired noncanonical NF-κB activity and defective lymphorganogenesis.
OBJECTIVE: We sought to establish genotype-phenotype correlation in patients with AD EDA-ID.
METHODS: A disease severity scoring system was devised. Stability of IκBα mutants was examined in transfected cells. Immunologic, biochemical, and gene expression analyses were performed to evaluate canonical and noncanonical NF-κB signaling in skin-derived fibroblasts.
RESULTS: Disease severity was greater in patients with IκBα point mutations than in those with truncation mutations. IκBα point mutants were expressed at significantly higher levels in transfectants compared with truncation mutants. Canonical NF-κB-dependent IL-6 secretion and upregulation of the NF-κB subunit 2/p100 and RELB proto-oncogene, NF-κB subunit (RelB) components of the noncanonical NF-κB pathway were diminished significantly more in patients with point mutations compared with those with truncations. Noncanonical NF-κB-driven generation of the transcriptionally active p100 cleavage product p52 and upregulation of CCL20, intercellular adhesion molecule 1 (ICAM1), and vascular cell adhesion molecule 1 (VCAM1), which are important for lymphorganogenesis, were diminished significantly more in LPS plus α-lymphotoxin β receptor-stimulated fibroblasts from patients with point mutations compared with those with truncations.
CONCLUSIONS: IκBα point mutants accumulate at higher levels compared with truncation mutants and are associated with more severe disease and greater impairment of canonical and noncanonical NF-κB activity in patients with AD EDA-ID.
Copyright © 2017 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Ectodermal dysplasia with immune deficiency; NF-κB inhibitor α; canonical nuclear factor κB pathway; hematopoietic stem cell transplantation; lymphorganogenesis; noncanonical nuclear factor κB pathway

Mesh:

Substances:

Year:  2017        PMID: 28629746      PMCID: PMC5733640          DOI: 10.1016/j.jaci.2017.05.030

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


  58 in total

Review 1.  Phosphorylation meets ubiquitination: the control of NF-[kappa]B activity.

Authors:  M Karin; Y Ben-Neriah
Journal:  Annu Rev Immunol       Date:  2000       Impact factor: 28.527

2.  Transcription of the RelB gene is regulated by NF-kappaB.

Authors:  G D Bren; N J Solan; H Miyoshi; K N Pennington; L J Pobst; C V Paya
Journal:  Oncogene       Date:  2001-11-22       Impact factor: 9.867

3.  A rapid screening method to detect autosomal-dominant ectodermal dysplasia with immune deficiency syndrome.

Authors:  Hidenori Ohnishi; Rie Miyata; Tomonori Suzuki; Touichiro Nose; Kazuo Kubota; Zenichiro Kato; Hideo Kaneko; Naomi Kondo
Journal:  J Allergy Clin Immunol       Date:  2011-11-10       Impact factor: 10.793

4.  Distinct roles in lymphoid organogenesis for lymphotoxins alpha and beta revealed in lymphotoxin beta-deficient mice.

Authors:  P A Koni; R Sacca; P Lawton; J L Browning; N H Ruddle; R A Flavell
Journal:  Immunity       Date:  1997-04       Impact factor: 31.745

Review 5.  NF-κB, the first quarter-century: remarkable progress and outstanding questions.

Authors:  Matthew S Hayden; Sankar Ghosh
Journal:  Genes Dev       Date:  2012-02-01       Impact factor: 11.361

Review 6.  The noncanonical NF-κB pathway.

Authors:  Shao-Cong Sun
Journal:  Immunol Rev       Date:  2012-03       Impact factor: 12.988

7.  Clinical characteristics and genotype-phenotype correlation in 62 patients with X-linked agammaglobulinemia.

Authors:  Pamela P W Lee; Tong-Xin Chen; Li-Ping Jiang; Koon-Wing Chan; Wanling Yang; Bee-Wah Lee; Wen-Chin Chiang; Xiang-Yuan Chen; Susanna F S Fok; Tsz-Leung Lee; Marco H K Ho; Xi-Qiang Yang; Yu-Lung Lau
Journal:  J Clin Immunol       Date:  2009-11-11       Impact factor: 8.317

8.  A novel gain-of-function IKBA mutation underlies ectodermal dysplasia with immunodeficiency and polyendocrinopathy.

Authors:  Lena F Schimke; Nikolaus Rieber; Stacey Rylaarsdam; Otávio Cabral-Marques; Nicholas Hubbard; Anne Puel; Laura Kallmann; Stephanie Anover Sombke; Gundula Notheis; Hans-Peter Schwarz; Birgit Kammer; Tomas Hökfelt; Reinald Repp; Capucine Picard; Jean-Laurent Casanova; Bernd H Belohradsky; Michael H Albert; Hans D Ochs; Ellen D Renner; Troy R Torgerson
Journal:  J Clin Immunol       Date:  2013-05-25       Impact factor: 8.317

9.  Lymphotoxin beta receptor signaling induces the chemokine CCL20 in intestinal epithelium.

Authors:  Martin Rumbo; Frédéric Sierro; Nathalie Debard; Jean-Pierre Kraehenbuhl; Daniela Finke
Journal:  Gastroenterology       Date:  2004-07       Impact factor: 22.682

10.  Defective lymphoid organogenesis underlies the immune deficiency caused by a heterozygous S32I mutation in IκBα.

Authors:  Jana L Mooster; Severine Le Bras; Michel J Massaad; Haifa Jabara; Juhan Yoon; Claire Galand; Balthasar A Heesters; Oliver T Burton; Hamid Mattoo; John Manis; Raif S Geha
Journal:  J Exp Med       Date:  2015-01-19       Impact factor: 14.307

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  9 in total

1.  IKBA S32 Mutations Underlie Ectodermal Dysplasia with Immunodeficiency and Severe Noninfectious Systemic Inflammation.

Authors:  Kunihiko Moriya; Yoji Sasahara; Hidenori Ohnishi; Tomoki Kawai; Hirokazu Kanegane
Journal:  J Clin Immunol       Date:  2018-06-14       Impact factor: 8.317

2.  Immunologic reconstitution following hematopoietic stem cell transplantation despite lymph node paucity in NF-κB-inducing kinase deficiency.

Authors:  Khaoula Ben Farhat; Mohammed F Alosaimi; Hiba Shendi; Suleiman Al-Hammadi; Jennifer Jones; Klaus Schwarz; Ansgar Schulz; Laila S Alawdah; Sandra Burchett; Sultan Albuhairi; Jennifer Whangbo; Neha Kwatra; Hanan E Shamseldin; Fowzan S Alkuraya; Janet Chou; Raif S Geha
Journal:  J Allergy Clin Immunol       Date:  2018-11-14       Impact factor: 10.793

3.  Clinical and Genetic Characteristics of Ectodermal Dysplasia in Four Indian Children.

Authors:  Divya Kamat; Rahul Mahajan; Debajyoti Chatterjee; Jaivinder Yadav; Rakesh Kumar; Devi Dayal; Dipankar De; Sanjeev Handa
Journal:  Indian J Dermatol       Date:  2022 Jan-Feb       Impact factor: 1.757

4.  Dominant-negative NFKBIA mutation promotes IL-1β production causing hepatic disease with severe immunodeficiency.

Authors:  Enrica Ek Tan; Richard A Hopkins; Chrissie K Lim; Saumya S Jamuar; Christina Ong; Koh C Thoon; Mark Ja Koh; Eun Mong Shin; Derrick Wq Lian; Madhushanee Weerasooriya; Christopher Zw Lee; Andreas Alvin Pumomo Soetedjo; Chang Siang Lim; Veonice B Au; Edmond Chua; Hui Yin Lee; Leigh Ann Jones; Sharmy S James; Nivashini Kaliaperumal; Jeffery Kwok; Ee Shien Tan; Biju Thomas; Lynn Xue Wu; Lena Ho; Anna Marie Fairhurst; Florent Ginhoux; Adrian Kk Teo; Yong Liang Zhang; Kok Huar Ong; Weimiao Yu; Byrappa Venkatesh; Vinay Tergaonkar; Bruno Reversade; Keh Chuang Chin; Ah Moy Tan; Woei Kang Liew; John E Connolly
Journal:  J Clin Invest       Date:  2020-11-02       Impact factor: 14.808

5.  A heterozygous N-terminal truncation mutation of NFKBIA results in an impaired NF-κB dependent inflammatory response.

Authors:  Wen Wen; Li Wang; Mengyue Deng; Yue Li; Xuemei Tang; Huawei Mao; Xiaodong Zhao
Journal:  Genes Dis       Date:  2021-04-03

Review 6.  Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases.

Authors:  Ruihan Yang; Yilan Mei; Yuhan Jiang; Huiling Li; Ruixi Zhao; Jian Sima; Yuyuan Yao
Journal:  Int J Mol Sci       Date:  2022-08-10       Impact factor: 6.208

Review 7.  Role of the NFκB-signaling pathway in cancer.

Authors:  Longzheng Xia; Shiming Tan; Yujuan Zhou; Jingguan Lin; Heran Wang; Linda Oyang; Yutong Tian; Lu Liu; Min Su; Hui Wang; Deliang Cao; Qianjin Liao
Journal:  Onco Targets Ther       Date:  2018-04-11       Impact factor: 4.147

8.  A novel 14q13.1-21.1 deletion identified by CNV-Seq in a patient with brain-lung-thyroid syndrome, tooth agenesis and immunodeficiency.

Authors:  Xuyun Hu; Jun Liu; Ruolan Guo; Jun Guo; Zhipeng Zhao; Wei Li; Baoping Xu; Chanjuan Hao
Journal:  Mol Cytogenet       Date:  2019-12-19       Impact factor: 2.009

Review 9.  EBMT/ESID inborn errors working party guidelines for hematopoietic stem cell transplantation for inborn errors of immunity.

Authors:  A C Lankester; M H Albert; C Booth; A R Gennery; T Güngör; M Hönig; E C Morris; D Moshous; B Neven; A Schulz; M Slatter; P Veys
Journal:  Bone Marrow Transplant       Date:  2021-07-05       Impact factor: 5.483

  9 in total

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