Literature DB >> 24122029

Clinical, immunological, and molecular characterization of hyper-IgM syndrome due to CD40 deficiency in eleven patients.

Bandar K Al-Saud, Zobaida Al-Sum, Hanadi Alassiri, Abdulaziz Al-Ghonaium, Saleh Al-Muhsen, Hasan Al-Dhekri, Rand Arnaout, Osama Alsmadi, Esteban Borrero, Asm'a Abu-Staiteh, Faisal Rawas, Hamoud Al-Mousa, Abbas Hawwari.   

Abstract

PURPOSE: Hyper-IgM syndrome due to CD40 deficiency (HIGM3) is a rare form of primary immunodeficiency with few reported cases. In this study, we further characterize the clinical, immunological, and molecular profiles of the disease in a cohort of 11 patients.
METHODS: Molecular genetic analysis and a comprehensive clinical review of patients diagnosed with HIGM3 at our tertiary care center from 1994 to 2011 were undertaken.
RESULTS: Eleven patients from seven families were enrolled. The patients had a median age of 9 years [ranging from 2 to 22 years old]. All 11 patients had recurrent chest infections at presentation. Pneumocystis jiroveci pneumonia was confirmed in three patients. Five patients had sclerosing cholangitis, and five patients had Cryptosporidium isolated from their stool. Six patients had nasal and sinus infections, and two of these patients had destructive nasal fungal infections. Eight patients had neutropenia. All of the patients had low IgG and normal or high IgM levels. IgA was undetectable in all but three patients. Two novel mutations were found: a splice site for intron 3 and a missense mutation located in the coding region of exon 3. Two patients underwent successful stem cell transplantation from a matched donor. Four patients are doing well on prophylaxis; two are very sick, one with protracted diarrhea and persistent Cryptosporidium and the other with neurological complications. Three patients died early in life as a result of severe sepsis.
CONCLUSIONS: To our knowledge, this report provides the largest cohort of patients with this disease with a very long follow-up period. Our cohort showed variable disease severity

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Year:  2013        PMID: 24122029     DOI: 10.1007/s10875-013-9951-9

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  27 in total

1.  Outcome of hematopoietic stem cell transplantation in hyper-IgM syndrome caused by CD40 deficiency.

Authors:  Necil Kutukculer; Serap Aksoylar; Savas Kansoy; Nazan Cetingul; Luigi D Notarangelo
Journal:  J Pediatr       Date:  2003-07       Impact factor: 4.406

2.  Clinical spectrum of X-linked hyper-IgM syndrome.

Authors:  J Levy; T Espanol-Boren; C Thomas; A Fischer; P Tovo; P Bordigoni; I Resnick; A Fasth; M Baer; L Gomez; E A Sanders; M D Tabone; D Plantaz; A Etzioni; V Monafo; M Abinun; L Hammarstrom; T Abrahamsen; A Jones; A Finn; T Klemola; E DeVries; O Sanal; M C Peitsch; L D Notarangelo
Journal:  J Pediatr       Date:  1997-07       Impact factor: 4.406

3.  Development of a rapid whole blood flow cytometry procedure for the diagnosis of X-linked hyper-IgM syndrome patients and carriers.

Authors:  M R O'Gorman; D Zaas; M Paniagua; V Corrochano; P R Scholl; L M Pachman
Journal:  Clin Immunol Immunopathol       Date:  1997-11

4.  Defective expression of the CD40 ligand in X chromosome-linked immunoglobulin deficiency with normal or elevated IgM.

Authors:  R Fuleihan; N Ramesh; R Loh; H Jabara; R S Rosen; T Chatila; S M Fu; I Stamenkovic; R S Geha
Journal:  Proc Natl Acad Sci U S A       Date:  1993-03-15       Impact factor: 11.205

5.  A boy with X-linked hyper-IgM syndrome and natural killer cell deficiency.

Authors:  B Ostenstad; S Giliani; O J Mellbye; B R Nilsen; T Abrahamsen
Journal:  Clin Exp Immunol       Date:  1997-02       Impact factor: 4.330

6.  Clinical and molecular characterization of X-linked hyper-IgM syndrome patients in China.

Authors:  Y An; J Xiao; L Jiang; X Yang; J Yu; X Zhao
Journal:  Scand J Immunol       Date:  2010-07       Impact factor: 3.487

7.  CD40 ligand mutations in x-linked immunodeficiency with hyper-IgM.

Authors:  J P DiSanto; J Y Bonnefoy; J F Gauchat; A Fischer; G de Saint Basile
Journal:  Nature       Date:  1993-02-11       Impact factor: 49.962

8.  Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination.

Authors:  Kohsuke Imai; Geir Slupphaug; Wen-I Lee; Patrick Revy; Shigeaki Nonoyama; Nadia Catalan; Leman Yel; Monique Forveille; Bodil Kavli; Hans E Krokan; Hans D Ochs; Alain Fischer; Anne Durandy
Journal:  Nat Immunol       Date:  2003-09-07       Impact factor: 25.606

9.  Hyper IgM syndrome associated with defective CD40-mediated B cell activation.

Authors:  M E Conley; M Larché; V R Bonagura; A R Lawton; R H Buckley; S M Fu; E Coustan-Smith; H G Herrod; D Campana
Journal:  J Clin Invest       Date:  1994-10       Impact factor: 14.808

10.  Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2).

Authors:  P Revy; T Muto; Y Levy; F Geissmann; A Plebani; O Sanal; N Catalan; M Forveille; R Dufourcq-Labelouse; A Gennery; I Tezcan; F Ersoy; H Kayserili; A G Ugazio; N Brousse; M Muramatsu; L D Notarangelo; K Kinoshita; T Honjo; A Fischer; A Durandy
Journal:  Cell       Date:  2000-09-01       Impact factor: 41.582

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  13 in total

1.  X-linked Hyper IgM Syndrome Presenting as Pulmonary Alveolar Proteinosis.

Authors:  Joel Gallagher; Juan Adams; Mary Hintermeyer; Troy R Torgerson; Jesus Lopez-Guisa; Hans D Ochs; Sara Szabo; Mina Salib; James Verbsky; John Routes
Journal:  J Clin Immunol       Date:  2016-06-20       Impact factor: 8.317

2.  Primary Immunodeficiency Diseases in Saudi Arabia: a Tertiary Care Hospital Experience over a Period of Three Years (2010-2013).

Authors:  Bandar Al-Saud; Hamoud Al-Mousa; Sulaiman Al Gazlan; Abdulaziz Al-Ghonaium; Rand Arnaout; Amal Al-Seraihy; Sahar Elshorbagi; Nazeema Elsayed; Jawad Afzal; Hasan Al-Dhekri; Saleh Al-Muhsen
Journal:  J Clin Immunol       Date:  2015-09-22       Impact factor: 8.317

Review 3.  Pathological and protective immunity to Pneumocystis infection.

Authors:  Taylor Eddens; Jay K Kolls
Journal:  Semin Immunopathol       Date:  2014-11-25       Impact factor: 9.623

Review 4.  Adaptive immunity to fungi.

Authors:  Akash Verma; Marcel Wüthrich; George Deepe; Bruce Klein
Journal:  Cold Spring Harb Perspect Med       Date:  2014-11-06       Impact factor: 6.915

Review 5.  Loss of NHEJ1 Protein Due to a Novel Splice Site Mutation in a Family Presenting with Combined Immunodeficiency, Microcephaly, and Growth Retardation and Literature Review.

Authors:  Farrukh Sheikh; Abbas Hawwari; Safa Alhissi; Sulaiman Al Gazlan; Hasan Al Dhekri; Agha M Rehan Khaliq; Esteban Borrero; Lina El-Baik; Rand Arnaout; Hamoud Al-Mousa; Anas M Alazami
Journal:  J Clin Immunol       Date:  2017-07-24       Impact factor: 8.317

6.  Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents.

Authors:  Romain Lévy; David Langlais; Vivien Béziat; Franck Rapaport; Geetha Rao; Tomi Lazarov; Mathieu Bourgey; Yu J Zhou; Coralie Briand; Kunihiko Moriya; Fatima Ailal; Danielle T Avery; Janet Markle; Ai Ing Lim; Masato Ogishi; Rui Yang; Simon Pelham; Mehdi Emam; Mélanie Migaud; Caroline Deswarte; Tanwir Habib; Luis R Saraiva; Eman A Moussa; Andrea Guennoun; Bertrand Boisson; Serkan Belkaya; Ruben Martinez-Barricarte; Jérémie Rosain; Aziz Belkadi; Sylvain Breton; Kathryn Payne; Ibtihal Benhsaien; Alessandro Plebani; Vassilios Lougaris; James P Di Santo; Bénédicte Neven; Laurent Abel; Cindy S Ma; Ahmed Aziz Bousfiha; Nico Marr; Jacinta Bustamante; Kang Liu; Philippe Gros; Frédéric Geissmann; Stuart G Tangye; Jean-Laurent Casanova; Anne Puel
Journal:  J Clin Invest       Date:  2021-09-01       Impact factor: 19.456

7.  Atypical Pneumocystis jirovecii pneumonia in previously untreated patients with CLL on single-agent ibrutinib.

Authors:  Inhye E Ahn; Theresa Jerussi; Mohammed Farooqui; Xin Tian; Adrian Wiestner; Juan Gea-Banacloche
Journal:  Blood       Date:  2016-08-08       Impact factor: 22.113

8.  TREC and KREC profiling as a representative of thymus and bone marrow output in patients with various inborn errors of immunity.

Authors:  M Dasouki; A Jabr; G AlDakheel; F Elbadaoui; A M Alazami; B Al-Saud; R Arnaout; H Aldhekri; I Alotaibi; H Al-Mousa; A Hawwari
Journal:  Clin Exp Immunol       Date:  2020-07-21       Impact factor: 4.330

9.  Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients.

Authors:  Hanen Ouadani; Imen Ben-Mustapha; Meriem Ben-ali; Leila Ben-khemis; Beya Larguèche; Raoudha Boussoffara; Sonia Maalej; Ilhem Fetni; Saida Hassayoun; Abdelmajid Mahfoudh; Fethi Mellouli; Sadok Yalaoui; Hatem Masmoudi; Mohamed Bejaoui; Mohamed-Ridha Barbouche
Journal:  Immunogenetics       Date:  2015-11-06       Impact factor: 2.846

10.  Hyperimmunoglobulin syndrome due to CD40 deficiency: possibly the first case from India.

Authors:  A Mishra; K Italia; M Gupta; M Desai; M Madkaikar
Journal:  J Postgrad Med       Date:  2015 Jan-Mar       Impact factor: 1.476

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