Literature DB >> 33717395

Inborn errors of immunity with atopic phenotypes: A practical guide for allergists.

Riccardo Castagnoli1,2,3, Vassilios Lougaris4, Giuliana Giardino5, Stefano Volpi6, Lucia Leonardi7, Francesco La Torre8, Silvia Federici9, Stefania Corrente10, Bianca Laura Cinicola7,11, Annarosa Soresina12, Caterina Cancrini13,14, Gian Luigi Marseglia1,2, Fabio Cardinale8.   

Abstract

Inborn errors of immunity (IEI) are a heterogeneous group of disorders, mainly resulting from mutations in genes associated with immunoregulation and immune host defense. These disorders are characterized by different combinations of recurrent infections, autoimmunity, inflammatory manifestations, lymphoproliferation, and malignancy. Interestingly, it has been increasingly observed that common allergic symptoms also can represent the expression of an underlying immunodeficiency and/or immune dysregulation. Very high IgE levels, peripheral or organ-specific hypereosinophilia, usually combined with a variety of atopic symptoms, may sometimes be the epiphenomenon of a monogenic disease. Therefore, allergists should be aware that severe and/or therapy-resistant atopic disorders might be the main clinical phenotype of some IEI. This could pave the way to target therapies, leading to better quality of life and improved survival in affected patients.
© 2021 The Author(s).

Entities:  

Keywords:  Allergy; Atopic phenotypes; Atopy; Inborn errors of immunity; Primary immunodeficiency

Year:  2021        PMID: 33717395      PMCID: PMC7907539          DOI: 10.1016/j.waojou.2021.100513

Source DB:  PubMed          Journal:  World Allergy Organ J        ISSN: 1939-4551            Impact factor:   4.084


  153 in total

1.  Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency.

Authors:  Manfred Fliegauf; Vanessa L Bryant; Natalie Frede; Charlotte Slade; See-Tarn Woon; Klaus Lehnert; Sandra Winzer; Alla Bulashevska; Thomas Scerri; Euphemia Leung; Anthony Jordan; Baerbel Keller; Esther de Vries; Hongzhi Cao; Fang Yang; Alejandro A Schäffer; Klaus Warnatz; Peter Browett; Jo Douglass; Rohan V Ameratunga; Jos W M van der Meer; Bodo Grimbacher
Journal:  Am J Hum Genet       Date:  2015-08-13       Impact factor: 11.025

2.  Variation in total and specific IgE: effects of ethnicity and socioeconomic status.

Authors:  Augusto A Litonjua; Juan C Celedón; Jonathan Hausmann; Margaret Nikolov; Diane Sredl; Louise Ryan; Thomas A E Platts-Mills; Scott T Weiss; Diane R Gold
Journal:  J Allergy Clin Immunol       Date:  2005-04       Impact factor: 10.793

3.  A multiinstitutional survey of the Wiskott-Aldrich syndrome.

Authors:  K E Sullivan; C A Mullen; R M Blaese; J A Winkelstein
Journal:  J Pediatr       Date:  1994-12       Impact factor: 4.406

Review 4.  SAM syndrome is characterized by extensive phenotypic heterogeneity.

Authors:  Shahar Taiber; Liat Samuelov; Janan Mohamad; Eran Cohen Barak; Ofer Sarig; Stavit Allon Shalev; Gilles Lestringant; Eli Sprecher
Journal:  Exp Dermatol       Date:  2018-07       Impact factor: 3.960

5.  A homozygous mucosa-associated lymphoid tissue 1 (MALT1) mutation in a family with combined immunodeficiency.

Authors:  Haifa H Jabara; Toshiro Ohsumi; Janet Chou; Michel J Massaad; Halli Benson; Andre Megarbane; Eliane Chouery; Raymond Mikhael; Oliver Gorka; Andreas Gewies; Pierre Portales; Toshinori Nakayama; Hiroyuki Hosokawa; Patrick Revy; Henry Herrod; Francoise Le Deist; Gerard Lefranc; Jürgen Ruland; Raif S Geha
Journal:  J Allergy Clin Immunol       Date:  2013-05-31       Impact factor: 10.793

Review 6.  The Wiskott-Aldrich syndrome: The actin cytoskeleton and immune cell function.

Authors:  Michael P Blundell; Austen Worth; Gerben Bouma; Adrian J Thrasher
Journal:  Dis Markers       Date:  2010       Impact factor: 3.434

7.  A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis.

Authors:  Tobias Schwerd; Stephen R F Twigg; Dominik Aschenbrenner; Santiago Manrique; Kerry A Miller; Indira B Taylor; Melania Capitani; Simon J McGowan; Elizabeth Sweeney; Astrid Weber; Liye Chen; Paul Bowness; Andrew Riordan; Andrew Cant; Alexandra F Freeman; Joshua D Milner; Steven M Holland; Natalie Frede; Miryam Müller; Dirk Schmidt-Arras; Bodo Grimbacher; Steven A Wall; E Yvonne Jones; Andrew O M Wilkie; Holm H Uhlig
Journal:  J Exp Med       Date:  2017-07-26       Impact factor: 14.307

8.  Congenital B cell lymphocytosis explained by novel germline CARD11 mutations.

Authors:  Andrew L Snow; Wenming Xiao; Jeffrey R Stinson; Wei Lu; Benjamin Chaigne-Delalande; Lixin Zheng; Stefania Pittaluga; Helen F Matthews; Roland Schmitz; Sameer Jhavar; Stefan Kuchen; Lela Kardava; Wei Wang; Ian T Lamborn; Huie Jing; Mark Raffeld; Susan Moir; Thomas A Fleisher; Louis M Staudt; Helen C Su; Michael J Lenardo
Journal:  J Exp Med       Date:  2012-11-05       Impact factor: 14.307

9.  Immune dysregulation, polyendocrinopathy, enteropathy, x-linked syndrome: a paradigm of immunodeficiency with autoimmunity.

Authors:  Federica Barzaghi; Laura Passerini; Rosa Bacchetta
Journal:  Front Immunol       Date:  2012-07-31       Impact factor: 7.561

10.  NF-κB1 Haploinsufficiency Causing Immunodeficiency and EBV-Driven Lymphoproliferation.

Authors:  Heidrun Boztug; Tatjana Hirschmugl; Wolfgang Holter; Karoly Lakatos; Leo Kager; Doris Trapin; Winfried Pickl; Elisabeth Förster-Waldl; Kaan Boztug
Journal:  J Clin Immunol       Date:  2016-06-23       Impact factor: 8.317

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  5 in total

Review 1.  Druggable monogenic immune defects hidden in diverse medical specialties: Focus on overlap syndromes.

Authors:  Valentina Boz; Chiara Zanchi; Laura Levantino; Guglielmo Riccio; Alberto Tommasini
Journal:  World J Clin Pediatr       Date:  2022-03-09

2.  Profound differences in IgE and IgG recognition of micro-arrayed allergens in hyper-IgE syndromes.

Authors:  Victoria Garib; Meriem Ben-Ali; Michael Kundi; Mirela Curin; Roukaya Yaakoubi; Imen Ben-Mustapha; Najla Mekki; Renate Froeschl; Thomas Perkmann; Rudolf Valenta; Mohamed-Ridha Barbouche
Journal:  Allergy       Date:  2021-11-02       Impact factor: 14.710

Review 3.  Diagnostic Challenges in Patients with Inborn Errors of Immunity with Different Manifestations of Immune Dysregulation.

Authors:  Karolina Pieniawska-Śmiech; Gerard Pasternak; Aleksandra Lewandowicz-Uszyńska; Marek Jutel
Journal:  J Clin Med       Date:  2022-07-20       Impact factor: 4.964

Review 4.  Primary atopic disorders and chronic skin disease.

Authors:  Bianca Laura Cinicola; Stefania Corrente; Riccardo Castagnoli; Vassilios Lougaris; Giuliana Giardino; Lucia Leonardi; Stefano Volpi; Francesco La Torre; Silvia Federici; Annarosa Soresina; Caterina Cancrini; Gian Luigi Marseglia; Fabio Cardinale
Journal:  Pediatr Allergy Immunol       Date:  2022-01       Impact factor: 5.464

5.  Tailored therapies for primary immunodeficiencies.

Authors:  Bianca Cinicola; Federica Pulvirenti; Giulia Brindisi; Gian Luigi Marseglia; Riccardo Castagnoli; Thomas Foiadelli; Carlo Caffarelli; Amelia Licari; Michele Miraglia Del Giudice; Anna Maria Zicari; Marzia Duse; Fabio Cardinale
Journal:  Acta Biomed       Date:  2021-11-29
  5 in total

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