Literature DB >> 28286158

Smith-Magenis Syndrome Patients Often Display Antibody Deficiency but Not Other Immune Pathologies.

Tiffany Perkins1, Jacob M Rosenberg2, Carole Le Coz3, Joseph T Alaimo4, Melissa Trofa3, Sureni V Mullegama4, Richard J Antaya5, Soma Jyonouchi3, Sarah H Elsea4, Paul J Utz6, Eric Meffre7, Neil Romberg8.   

Abstract

BACKGROUND: Smith-Magenis syndrome (SMS) is a complex neurobehavioral disorder associated with recurrent otitis. Most SMS cases result from heterozygous interstitial chromosome 17p11.2 deletions that encompass not only the intellectual disability gene retinoic acid-induced 1 but also other genes associated with immunodeficiency, autoimmunity, and/or malignancy.
OBJECTIVES: The goals of this study were to describe the immunological consequence of 17p11.2 deletions by determining the prevalence of immunological diseases in subjects with SMS and by assessing their immune systems via laboratory methods.
METHODS: We assessed clinical histories of 76 subjects with SMS with heterozygous 17p11.2 deletions and performed in-depth immunological testing on 25 representative cohort members. Laboratory testing included determination of serum antibody concentrations, vaccine titers, and lymphocyte subset frequencies. Detailed reactivity profiles of SMS serum antibodies were performed using custom-made antigen microarrays.
RESULTS: Of 76 subjects with SMS, 74 reported recurrent infections including otitis (88%), pneumonia (47%), sinusitis (42%), and gastroenteritis (34%). Infections were associated with worsening SMS-related neurobehavioral symptoms. The prevalence of autoimmune and atopic diseases was not increased. Malignancy was not reported. Laboratory evaluation revealed most subjects with SMS to be deficient of isotype-switched memory B cells and many to lack protective antipneumococcal antibodies. SMS antibodies were not more reactive than control antibodies to self-antigens.
CONCLUSIONS: Patients with SMS with heterozygous 17p.11.2 deletions display an increased susceptibility to sinopulmonary infections, but not to autoimmune, allergic, or malignant diseases. SMS sera display an antibody reactivity profile favoring neither recognition of pathogen-associated antigens nor self-antigens. Prophylactic strategies to prevent infections may also provide neurobehavioral benefits to selected patients with SMS.
Copyright © 2017 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Autoantibody; B-cell tolerance; Chromosome 17p11.2 deletion; FLCN; Immune deficiency; Smith-Magenis syndrome; TNFRSF13B; TOM1L2

Mesh:

Substances:

Year:  2017        PMID: 28286158      PMCID: PMC5591748          DOI: 10.1016/j.jaip.2017.01.028

Source DB:  PubMed          Journal:  J Allergy Clin Immunol Pract


  38 in total

1.  Otorhinolaringologic manifestation of Smith-Magenis syndrome.

Authors:  M Di Cicco; R Padoan; G Felisati; D Dilani; E Moretti; S Guerneri; A Selicorni
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2001-06-07       Impact factor: 1.675

2.  Regulation of the T-independent humoral response by TACI.

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Review 3.  How I treat common variable immune deficiency.

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4.  Transmembrane activator and CAML interactor (TACI) haploinsufficiency results in B-cell dysfunction in patients with Smith-Magenis syndrome.

Authors:  Javier Chinen; Monica Martinez-Gallo; Wenli Gu; Montserrat Cols; Andrea Cerutti; Lin Radigan; Li Zhang; Lorraine Potocki; Marjorie Withers; James R Lupski; Charlotte Cunningham-Rundles
Journal:  J Allergy Clin Immunol       Date:  2011-04-22       Impact factor: 10.793

5.  TNF receptor superfamily member 13b (TNFRSF13B) hemizygosity reveals transmembrane activator and CAML interactor haploinsufficiency at later stages of B-cell development.

Authors:  Neil Romberg; Manmeet Virdee; Nicolas Chamberlain; Tyler Oe; Jean-Nicolas Schickel; Tiffany Perkins; Tineke Cantaert; Rima Rachid; Sally Rosengren; Regina Palazzo; Raif Geha; Charlotte Cunningham-Rundles; Eric Meffre
Journal:  J Allergy Clin Immunol       Date:  2015-06-19       Impact factor: 10.793

6.  Interferon-α induction and detection of anti-ro, anti-la, anti-sm, and anti-rnp autoantibodies by autoantigen microarray analysis in juvenile dermatomyositis.

Authors:  Imelda Balboni; Timothy B Niewold; Gabrielle Morgan; Cindy Limb; Maija-Leena Eloranta; Lars Rönnblom; Paul J Utz; Lauren M Pachman
Journal:  Arthritis Rheum       Date:  2013-09

7.  Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease.

Authors:  Klaus Warnatz; Axel Denz; Ruth Dräger; Moritz Braun; Christoph Groth; Guido Wolff-Vorbeck; Hermann Eibel; Michael Schlesier; Hans Hartmut Peter
Journal:  Blood       Date:  2002-03-01       Impact factor: 22.113

8.  Protein microarrays identify disease-specific anti-cytokine autoantibody profiles in the landscape of immunodeficiency.

Authors:  Jacob M Rosenberg; Jordan V Price; Gabriela Barcenas-Morales; Lourdes Ceron-Gutierrez; Sophie Davies; Dinakantha S Kumararatne; Rainer Döffinger; Paul J Utz
Journal:  J Allergy Clin Immunol       Date:  2015-09-11       Impact factor: 10.793

9.  Transmembrane activator and calcium modulator and cyclophilin ligand interactor enhances CD40-driven plasma cell differentiation.

Authors:  Emanuela Castigli; Stephen A Wilson; Abdallah Elkhal; Esra Ozcan; Lilit Garibyan; Raif S Geha
Journal:  J Allergy Clin Immunol       Date:  2007-08-08       Impact factor: 10.793

10.  The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88.

Authors:  Bing He; Raul Santamaria; Weifeng Xu; Montserrat Cols; Kang Chen; Irene Puga; Meimei Shan; Huabao Xiong; James B Bussel; April Chiu; Anne Puel; Jeanine Reichenbach; László Marodi; Rainer Döffinger; Julia Vasconcelos; Andrew Issekutz; Jens Krause; Graham Davies; Xiaoxia Li; Bodo Grimbacher; Alessandro Plebani; Eric Meffre; Capucine Picard; Charlotte Cunningham-Rundles; Jean-Laurent Casanova; Andrea Cerutti
Journal:  Nat Immunol       Date:  2010-08-01       Impact factor: 25.606

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  3 in total

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Review 2.  Smith-Magenis Syndrome-Clinical Review, Biological Background and Related Disorders.

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Journal:  Genes (Basel)       Date:  2022-02-11       Impact factor: 4.096

3.  Two Monogenetic Disorders, Activated PI3-Kinase-δ Syndrome 2 and Smith-Magenis Syndrome, in One Patient: Case Report and a Literature Review of Neurodevelopmental Impact in Primary Immunodeficiencies Associated With Disturbed PI3K Signaling.

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Journal:  Front Pediatr       Date:  2021-06-24       Impact factor: 3.418

  3 in total

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