Literature DB >> 31486986

Novel Developments in Primary Immunodeficiencies (PID)-a Rheumatological Perspective.

Helen Leavis1, Jochen Zwerina2, Bernhard Manger3, Ruth D E Fritsch-Stork4,5.   

Abstract

PURPOSE OF REVIEW: The purpose of this review is to provide an overview of the most relevant new disorders, disease entities, or disease phenotypes of primary immune deficiency disorders (PID) for the interested rheumatologist, using the new phenotypic classification by the IUIS (International Union of Immunological Societies) as practical guide. RECENT
FINDINGS: Newly recognized disorders of immune dysregulation with underlying mutations in genes pertaining to the function of regulatory T cells (e.g., CTLA-4, LRBA, or BACH2) are characterized by multiple autoimmune diseases-mostly autoimmune cytopenia-combined with an increased susceptibility to infections due to hypogammaglobulinemia. On the other hand, new mutations (e.g., in NF-kB1, PI3Kδ, PI3KR1, PKCδ) leading to the clinical picture of CVID (common variable immmune deficiency) have been shown to increasingly associate with autoimmune diseases. The mutual association of autoimmune diseases with PID warrants increased awareness of immunodeficiencies when diagnosing autoimmune diseases with a possible need to initiate appropriate genetic tests.

Entities:  

Keywords:  APDS; CTLA-4 haploinsufficiency; CVID; DADA2; LRBA indusfficiency; NF-kB deficiency

Mesh:

Year:  2019        PMID: 31486986     DOI: 10.1007/s11926-019-0854-5

Source DB:  PubMed          Journal:  Curr Rheumatol Rep        ISSN: 1523-3774            Impact factor:   4.592


  94 in total

1.  Expansion of CD19(hi)CD21(lo/neg) B cells in common variable immunodeficiency (CVID) patients with autoimmune cytopenia.

Authors:  Klaus Warnatz; Claudia Wehr; Ruth Dräger; Sigune Schmidt; Hermann Eibel; Michael Schlesier; Hans-Hartmut Peter
Journal:  Immunobiology       Date:  2002-12       Impact factor: 3.144

2.  STAT3 mutations in the hyper-IgE syndrome.

Authors:  Steven M Holland; Frank R DeLeo; Houda Z Elloumi; Amy P Hsu; Gulbu Uzel; Nina Brodsky; Alexandra F Freeman; Andrew Demidowich; Joie Davis; Maria L Turner; Victoria L Anderson; Dirk N Darnell; Pamela A Welch; Douglas B Kuhns; David M Frucht; Harry L Malech; John I Gallin; Scott D Kobayashi; Adeline R Whitney; Jovanka M Voyich; James M Musser; Cristina Woellner; Alejandro A Schäffer; Jennifer M Puck; Bodo Grimbacher
Journal:  N Engl J Med       Date:  2007-09-19       Impact factor: 91.245

3.  TACI is mutant in common variable immunodeficiency and IgA deficiency.

Authors:  Emanuela Castigli; Stephen A Wilson; Lilit Garibyan; Rima Rachid; Francisco Bonilla; Lynda Schneider; Raif S Geha
Journal:  Nat Genet       Date:  2005-07-10       Impact factor: 38.330

4.  The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.

Authors:  C L Bennett; J Christie; F Ramsdell; M E Brunkow; P J Ferguson; L Whitesell; T E Kelly; F T Saulsbury; P F Chance; H D Ochs
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

5.  B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.

Authors:  Klaus Warnatz; Ulrich Salzer; Marta Rizzi; Beate Fischer; Sylvia Gutenberger; Joachim Böhm; Anne-Kathrin Kienzler; Qiang Pan-Hammarström; Lennart Hammarström; Mirzokhid Rakhmanov; Michael Schlesier; Bodo Grimbacher; Hans-Hartmut Peter; Hermann Eibel
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-06       Impact factor: 11.205

6.  Projection of an immunological self shadow within the thymus by the aire protein.

Authors:  Mark S Anderson; Emily S Venanzi; Ludger Klein; Zhibin Chen; Stuart P Berzins; Shannon J Turley; Harald von Boehmer; Roderick Bronson; Andrée Dierich; Christophe Benoist; Diane Mathis
Journal:  Science       Date:  2002-10-10       Impact factor: 47.728

7.  An antibody-deficiency syndrome due to mutations in the CD19 gene.

Authors:  Menno C van Zelm; Ismail Reisli; Mirjam van der Burg; Diana Castaño; Carel J M van Noesel; Maarten J D van Tol; Cristina Woellner; Bodo Grimbacher; Pablo J Patiño; Jacques J M van Dongen; José L Franco
Journal:  N Engl J Med       Date:  2006-05-04       Impact factor: 91.245

8.  Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency.

Authors:  Bodo Grimbacher; Andreas Hutloff; Michael Schlesier; Erik Glocker; Klaus Warnatz; Ruth Dräger; Hermann Eibel; Beate Fischer; Alejandro A Schäffer; Hans W Mages; Richard A Kroczek; Hans H Peter
Journal:  Nat Immunol       Date:  2003-02-10       Impact factor: 25.606

9.  A new CD21low B cell population in the peripheral blood of patients with SLE.

Authors:  Claudia Wehr; Hermann Eibel; Madhan Masilamani; Harald Illges; Michael Schlesier; Hans-Hartmut Peter; Klaus Warnatz
Journal:  Clin Immunol       Date:  2004-11       Impact factor: 3.969

10.  The EUROclass trial: defining subgroups in common variable immunodeficiency.

Authors:  Claudia Wehr; Teemu Kivioja; Christian Schmitt; Berne Ferry; Torsten Witte; Efrem Eren; Marcela Vlkova; Manuel Hernandez; Drahomira Detkova; Philip R Bos; Gonke Poerksen; Horst von Bernuth; Ulrich Baumann; Sigune Goldacker; Sylvia Gutenberger; Michael Schlesier; Florence Bergeron-van der Cruyssen; Magali Le Garff; Patrice Debré; Roland Jacobs; John Jones; Elizabeth Bateman; Jiri Litzman; P Martin van Hagen; Alessandro Plebani; Reinhold E Schmidt; Vojtech Thon; Isabella Quinti; Teresa Espanol; A David Webster; Helen Chapel; Mauno Vihinen; Eric Oksenhendler; Hans Hartmut Peter; Klaus Warnatz
Journal:  Blood       Date:  2007-09-26       Impact factor: 22.113

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  6 in total

Review 1.  Beyond Infections: New Warning Signs for Inborn Errors of Immunity in Children.

Authors:  Giorgio Costagliola; Diego G Peroni; Rita Consolini
Journal:  Front Pediatr       Date:  2022-06-10       Impact factor: 3.569

2.  Spontaneous Myocarditis in Mice Predisposed to Autoimmune Disease: Including Vaccination-Induced Onset.

Authors:  Takuma Hayashi; Motoki Ichikawa; Ikuo Konishi
Journal:  Biomedicines       Date:  2022-06-18

Review 3.  Comprehensive comparison between 222 CTLA-4 haploinsufficiency and 212 LRBA deficiency patients: a systematic review.

Authors:  M Jamee; S Hosseinzadeh; N Sharifinejad; M Zaki-Dizaji; M Matloubi; M Hasani; S Baris; M Alsabbagh; B Lo; G Azizi
Journal:  Clin Exp Immunol       Date:  2021-05-03       Impact factor: 5.732

Review 4.  Lymphadenopathy at the crossroad between immunodeficiency and autoinflammation: An intriguing challenge.

Authors:  Giorgio Costagliola; Rita Consolini
Journal:  Clin Exp Immunol       Date:  2021-06-20       Impact factor: 4.330

5.  Update in Primary Immunodeficiencies.

Authors:  Lucia Leonardi; Beatrice Rivalta; Caterina Cancrini; Elena Chiappini; Claudio Cravidi; Carlo Caffarelli; Sara Manti; Mauro Calvani; Alberto Martelli; Michele Miraglia Del Giudice; Marzia Duse; Gian Luigi Marseglia; Fabio Cardinale
Journal:  Acta Biomed       Date:  2020-09-15

6.  Targeted NGS Yields Plentiful Ultra-Rare Variants in Inborn Errors of Immunity Patients.

Authors:  Alice Grossi; Maurizio Miano; Marina Lanciotti; Francesca Fioredda; Daniela Guardo; Elena Palmisani; Paola Terranova; Giuseppe Santamaria; Francesco Caroli; Roberta Caorsi; Stefano Volpi; Marco Gattorno; Carlo Dufour; Isabella Ceccherini
Journal:  Genes (Basel)       Date:  2021-08-24       Impact factor: 4.096

  6 in total

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