Literature DB >> 21535335

Two SCID cases with Cernunnos-XLF deficiency successfully treated by hematopoietic stem cell transplantation.

Deniz Çağdaş1, Tuba Turul Özgür, Gülten Türkkanı Asal, Patrick Revy, Jean-Pierre De Villartay, Mirjam van der Burg, Özden Sanal, Ilhan Tezcan.   

Abstract

SCID affects T and B cell differentiation and functions, presenting with severe opportunistic infections in the early postnatal period. It is fatal unless stem cell transplantation is performed. RS SCID forms are caused by defects in the NHEJ pathway, the enzymatic process required for the repair of DNA double-strand breaks. Cernunnos-XLF defect is one of the defects in this pathway. Here, we present two patients with Cernunnos-XLF defect, both having microcephaly, prominent growth retardation, and T-B-NK+SCID, one of whom had AHA. These patients received hematopoietic stem cells from HLA identical related donor without conditioning regimen and recovered without any complication. Now, both of the patients are well and alive seven and one yr after transplantation, respectively. A remarkable observation was the severe diarrhea that occurred in both patients soon after transplantation.
© 2011 John Wiley & Sons A/S.

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Year:  2011        PMID: 21535335     DOI: 10.1111/j.1399-3046.2011.01491.x

Source DB:  PubMed          Journal:  Pediatr Transplant        ISSN: 1397-3142


  10 in total

Review 1.  Hematopoietic stem cell transplantation for primary immunodeficiencies.

Authors:  Elizabeth Kang; Andrew Gennery
Journal:  Hematol Oncol Clin North Am       Date:  2014-09-16       Impact factor: 3.722

2.  Radiation-sensitive severe combined immunodeficiency: The arguments for and against conditioning before hematopoietic cell transplantation--what to do?

Authors:  Morton J Cowan; Andrew R Gennery
Journal:  J Allergy Clin Immunol       Date:  2015-06-06       Impact factor: 10.793

Review 3.  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

4.  Outcome of hematopoietic cell transplantation for DNA double-strand break repair disorders.

Authors:  James Slack; Michael H Albert; Dmitry Balashov; Bernd H Belohradsky; Alice Bertaina; Jack Bleesing; Claire Booth; Jochen Buechner; Rebecca H Buckley; Marie Ouachée-Chardin; Elena Deripapa; Katarzyna Drabko; Mary Eapen; Tobias Feuchtinger; Andrea Finocchi; H Bobby Gaspar; Sujal Ghosh; Alfred Gillio; Luis I Gonzalez-Granado; Eyal Grunebaum; Tayfun Güngör; Carsten Heilmann; Merja Helminen; Kohei Higuchi; Kohsuke Imai; Krzysztof Kalwak; Nubuo Kanazawa; Gülsün Karasu; Zeynep Y Kucuk; Alexandra Laberko; Andrzej Lange; Nizar Mahlaoui; Roland Meisel; D Moshous; Hideki Muramatsu; Suhag Parikh; Srdjan Pasic; Irene Schmid; Catharina Schuetz; Ansgar Schulz; Kirk R Schultz; Peter J Shaw; Mary A Slatter; Karl-Walter Sykora; Shinobu Tamura; Mervi Taskinen; Angela Wawer; Beata Wolska-Kuśnierz; Morton J Cowan; Alain Fischer; Andrew R Gennery
Journal:  J Allergy Clin Immunol       Date:  2017-04-07       Impact factor: 10.793

Review 5.  Role of non-homologous end joining in V(D)J recombination.

Authors:  Shruti Malu; Vidyasagar Malshetty; Dailia Francis; Patricia Cortes
Journal:  Immunol Res       Date:  2012-12       Impact factor: 2.829

6.  Rescue of DNA-PK Signaling and T-Cell Differentiation by Targeted Genome Editing in a prkdc Deficient iPSC Disease Model.

Authors:  Shamim H Rahman; Johannes Kuehle; Christian Reimann; Tafadzwa Mlambo; Jamal Alzubi; Morgan L Maeder; Heimo Riedel; Paul Fisch; Tobias Cantz; Cornelia Rudolph; Claudio Mussolino; J Keith Joung; Axel Schambach; Toni Cathomen
Journal:  PLoS Genet       Date:  2015-05-22       Impact factor: 5.917

7.  An immunocompetent patient with a nonsense mutation in NHEJ1 gene.

Authors:  Hossein Esmaeilzadeh; Mohammad Reza Bordbar; Zahra Hojaji; Parham Habibzadeh; Dorna Afshinfar; Mohammad Miryounesi; Majid Fardaei; Mohammad Ali Faghihi
Journal:  BMC Med Genet       Date:  2019-03-21       Impact factor: 2.103

Review 8.  Cernunnos defect in an Iranian patient with T- B+ NK+ severe combined immunodeficiency: A case report and review of the literature.

Authors:  Mahnaz Jamee; Nasrin Khakbazan Fard; Shahrzad Fallah; Zahra Golchehre; Mazdak Fallahi; Bibi Shahin Shamsian; Samin Sharafian; Zahra Chavoshzadeh
Journal:  Mol Genet Genomic Med       Date:  2022-06-02       Impact factor: 2.473

9.  Cernunnos/XLF Deficiency: A Syndromic Primary Immunodeficiency.

Authors:  Funda Erol Cipe; Cigdem Aydogmus; Arzu Babayigit Hocaoglu; Merve Kilic; Gul Demet Kaya; Elif Yilmaz Gulec
Journal:  Case Rep Pediatr       Date:  2014-01-08

Review 10.  Hematopoietic Stem Cell Transplantation for DNA Double Strand Breakage Repair Disorders.

Authors:  Beata Wolska-Kuśnierz; Andrew R Gennery
Journal:  Front Pediatr       Date:  2020-01-15       Impact factor: 3.418

  10 in total

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