Literature DB >> 36258138

Hypoparathyroidism-Retardation-Dysmorphism Syndrome due to a Variant in the Tubulin-Specific Chaperone E Gene as a Cause of Combined Immune Deficiency.

Odeya David1,2,3, Eyal Kristal4,5, Galina Ling2,3, Arnon Broides2,3,6, Nurit Hadad3,7,8, George Shubinsky3,8, Amit Nahum3,6,9,10.   

Abstract

BACKGROUND: Hypoparathyroidism-retardation-dysmorphism (HRD) syndrome is a disease composed of hypoparathyroidism, growth retardation, severe developmental delay, and typical dysmorphic features caused by the tubulin-specific chaperone E gene variant. Many patients succumb in infancy to HRD due to overwhelming infections mainly caused by Pneumococcus spp. Knowledge related to the immune system in these patients is scarce.
PURPOSE: To define the immune phenotype of a cohort of HRD patients including their cellular, humoral, and neutrophil functions.
METHODS: The study included HRD patients followed at Soroka University Medical Center. Clinical and immunological data were obtained, including immunoglobulin concentrations, specific antibody titers, lymphocyte subpopulations, lymphocyte proliferation, and neutrophil functions.
RESULTS: Nine patients (5 females and 4 males) were enrolled, aged 6 months to 15 years. All received amoxicillin prophylaxis as part of a routine established previously. Three patients had bacteremia with Klebsiella, Shigella spp., and Candida. Three patients had confirmed coronavirus disease 19 (COVID-19), and two of them died from this infection. All patients had normal blood counts. Patients showed high total IgA and IgE levels, low anti-pneumococcal antibodies in spite of a routine vaccination schedule, and reduced frequency of naive B cells with increased frequency of CD21lowCD27- B cells. All patients had abnormal T-cell population distributions, including reduced terminally differentiated effector memory CD8, inverted CD4/CD8 ratios, and impaired phytohemagglutinin (PHA)-induced lymphocyte proliferation. Neutrophil superoxide production and chemotaxis were normal in all patients tested.
CONCLUSION: HRD is a combined immunodeficiency disease with syndromic features, manifesting in severe invasive bacterial and viral infections.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Hypoparathyroidism-Retardation-Dysmorphism (HRD) syndrome; Inborn Errors of Immunity (IEI); Sanjad–Sakati syndrome; combined immune deficiency

Year:  2022        PMID: 36258138      PMCID: PMC9579628          DOI: 10.1007/s10875-022-01380-9

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.542


  21 in total

1.  Control of type I interferon-induced cell death by Orai1-mediated calcium entry in T cells.

Authors:  Chanyu Yue; Jonathan Soboloff; Ana M Gamero
Journal:  J Biol Chem       Date:  2011-12-05       Impact factor: 5.157

Review 2.  Orchestrating cytoskeleton and intracellular vesicle traffic to build functional immunological synapses.

Authors:  Helena Soares; Rémi Lasserre; Andrés Alcover
Journal:  Immunol Rev       Date:  2013-11       Impact factor: 12.988

Review 3.  Calcium signalling in T cells.

Authors:  Mohamed Trebak; Jean-Pierre Kinet
Journal:  Nat Rev Immunol       Date:  2019-03       Impact factor: 53.106

Review 4.  Coordinate control of cytoskeletal remodeling and calcium mobilization during T-cell activation.

Authors:  Alexander Babich; Janis K Burkhardt
Journal:  Immunol Rev       Date:  2013-11       Impact factor: 12.988

5.  Autoimmune thyroiditis associated with Sanjad-Sakati syndrome: A call for regular thyroid screening.

Authors:  Abeer M Anteet; Sharifah T Al Issa; Amer O Al-Ali; Hessah M Al-Otaibi; Sarar Mohamed; Amir Babiker; Nasir A M Al-Jurayyan
Journal:  Sudan J Paediatr       Date:  2016

Review 6.  Diseases caused by mutations in ORAI1 and STIM1.

Authors:  Rodrigo S Lacruz; Stefan Feske
Journal:  Ann N Y Acad Sci       Date:  2015-10-15       Impact factor: 5.691

7.  Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome.

Authors:  Ruti Parvari; Eli Hershkovitz; Nili Grossman; Rafael Gorodischer; Bart Loeys; Alexandra Zecic; Geert Mortier; Simon Gregory; Reuven Sharony; Marios Kambouris; Nadia Sakati; Brian F Meyer; Aida I Al Aqeel; Abdul Karim Al Humaidan; Fatma Al Zanhrani; Abdulrahman Al Swaid; Johara Al Othman; George A Diaz; Rory Weiner; K Tahseen S Khan; Ronald Gordon; Bruce D Gelb
Journal:  Nat Genet       Date:  2002-10-21       Impact factor: 38.330

8.  Short stature, mental retardation, and hypoparathyroidism: a new syndrome.

Authors:  R J Richardson; J M Kirk
Journal:  Arch Dis Child       Date:  1990-10       Impact factor: 3.791

9.  The exocyst controls lysosome secretion and antigen extraction at the immune synapse of B cells.

Authors:  Juan José Sáez; Jheimmy Diaz; Jorge Ibañez; Juan Pablo Bozo; Fernanda Cabrera Reyes; Martina Alamo; François-Xavier Gobert; Dorian Obino; María Rosa Bono; Ana-María Lennon-Duménil; Charles Yeaman; María-Isabel Yuseff
Journal:  J Cell Biol       Date:  2019-06-13       Impact factor: 10.539

10.  Hypoparathyroidism-retardation-dysmorphism syndrome-Clinical insights from a large longitudinal cohort in a single medical center.

Authors:  Odeya David; Rotem Agur; Rosa Novoa; David Shaki; Dganit Walker; Lior Carmon; Marina Eskin-Schwartz; Ohad S Birk; Galina Ling; Ruth Schreiber; Neta Loewenthal; Alon Haim; Eli Hershkovitz
Journal:  Front Pediatr       Date:  2022-07-22       Impact factor: 3.569

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