Literature DB >> 28392333

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

James Slack1, Michael H Albert2, Dmitry Balashov3, Bernd H Belohradsky2, Alice Bertaina4, Jack Bleesing5, Claire Booth6, Jochen Buechner7, Rebecca H Buckley8, Marie Ouachée-Chardin9, Elena Deripapa3, Katarzyna Drabko10, Mary Eapen11, Tobias Feuchtinger12, Andrea Finocchi13, H Bobby Gaspar6, Sujal Ghosh14, Alfred Gillio15, Luis I Gonzalez-Granado16, Eyal Grunebaum17, Tayfun Güngör18, Carsten Heilmann19, Merja Helminen20, Kohei Higuchi21, Kohsuke Imai22, Krzysztof Kalwak23, Nubuo Kanazawa24, Gülsün Karasu25, Zeynep Y Kucuk5, Alexandra Laberko3, Andrzej Lange26, Nizar Mahlaoui27, Roland Meisel28, D Moshous29, Hideki Muramatsu30, Suhag Parikh31, Srdjan Pasic32, Irene Schmid2, Catharina Schuetz33, Ansgar Schulz33, Kirk R Schultz34, Peter J Shaw35, Mary A Slatter36, Karl-Walter Sykora37, Shinobu Tamura38, Mervi Taskinen39, Angela Wawer40, Beata Wolska-Kuśnierz41, Morton J Cowan42, Alain Fischer29, Andrew R Gennery43.   

Abstract

BACKGROUND: Rare DNA breakage repair disorders predispose to infection and lymphoreticular malignancies. Hematopoietic cell transplantation (HCT) is curative, but coadministered chemotherapy or radiotherapy is damaging because of systemic radiosensitivity. We collected HCT outcome data for Nijmegen breakage syndrome, DNA ligase IV deficiency, Cernunnos-XRCC4-like factor (Cernunnos-XLF) deficiency, and ataxia-telangiectasia (AT).
METHODS: Data from 38 centers worldwide, including indication, donor, conditioning regimen, graft-versus-host disease, and outcome, were analyzed. Conditioning was classified as myeloablative conditioning (MAC) if it contained radiotherapy or alkylators and reduced-intensity conditioning (RIC) if no alkylators and/or 150 mg/m2 fludarabine or less and 40 mg/kg cyclophosphamide or less were used.
RESULTS: Fifty-five new, 14 updated, and 18 previously published patients were analyzed. Median age at HCT was 48 months (range, 1.5-552 months). Twenty-nine patients underwent transplantation for infection, 21 had malignancy, 13 had bone marrow failure, 13 received pre-emptive transplantation, 5 had multiple indications, and 6 had no information. Twenty-two received MAC, 59 received RIC, and 4 were infused; information was unavailable for 2 patients. Seventy-three of 77 patients with DNA ligase IV deficiency, Cernunnos-XLF deficiency, or Nijmegen breakage syndrome received conditioning. Survival was 53 (69%) of 77 and was worse for those receiving MAC than for those receiving RIC (P = .006). Most deaths occurred early after transplantation, suggesting poor tolerance of conditioning. Survival in patients with AT was 25%. Forty-one (49%) of 83 patients experienced acute GvHD, which was less frequent in those receiving RIC compared with those receiving MAC (26/56 [46%] vs 12/21 [57%], P = .45). Median follow-up was 35 months (range, 2-168 months). No secondary malignancies were reported during 15 years of follow-up. Growth and developmental delay remained after HCT; immune-mediated complications resolved.
CONCLUSION: RIC HCT resolves DNA repair disorder-associated immunodeficiency. Long-term follow-up is required for secondary malignancy surveillance. Routine HCT for AT is not recommended.
Copyright © 2017 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Ataxia-telangiectasia; Cernunnos-XLF deficiency; DNA ligase IV deficiency; DNA repair disorders; Nijmegen breakage syndrome; hematopoietic stem cell transplantation

Mesh:

Year:  2017        PMID: 28392333      PMCID: PMC5632132          DOI: 10.1016/j.jaci.2017.02.036

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


  40 in total

1.  Omenn syndrome is associated with mutations in DNA ligase IV.

Authors:  Eyal Grunebaum; Andrea Bates; Chaim M Roifman
Journal:  J Allergy Clin Immunol       Date:  2008-10-09       Impact factor: 10.793

Review 2.  Detection and repair of ionizing radiation-induced DNA double strand breaks: new developments in nonhomologous end joining.

Authors:  Chen Wang; Susan P Lees-Miller
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3.  Reprint of "The clinical impact of deficiency in DNA non-homologous end-joining".

Authors:  Lisa Woodbine; Andrew R Gennery; Penny A Jeggo
Journal:  DNA Repair (Amst)       Date:  2014-04-26

4.  A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutation.

Authors:  Mirjam van der Burg; Lieneke R van Veelen; Nicole S Verkaik; Wouter W Wiegant; Nico G Hartwig; Barbara H Barendregt; Linda Brugmans; Anja Raams; Nicolaas G J Jaspers; Malgorzata Z Zdzienicka; Jacques J M van Dongen; Dik C van Gent
Journal:  J Clin Invest       Date:  2005-12-15       Impact factor: 14.808

5.  Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.

Authors:  D Moshous; I Callebaut; R de Chasseval; B Corneo; M Cavazzana-Calvo; F Le Deist; I Tezcan; O Sanal; Y Bertrand; N Philippe; A Fischer; J P de Villartay
Journal:  Cell       Date:  2001-04-20       Impact factor: 41.582

6.  Nonhomologous end joining and V(D)J recombination require an additional factor.

Authors:  Y Dai; B Kysela; L A Hanakahi; K Manolis; E Riballo; M Stumm; T O Harville; S C West; M A Oettinger; P A Jeggo
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-25       Impact factor: 11.205

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Journal:  J Clin Microbiol       Date:  2013-06-12       Impact factor: 5.948

8.  Characteristics and outcome of early-onset, severe forms of Wiskott-Aldrich syndrome.

Authors:  Nizar Mahlaoui; Isabelle Pellier; Cécile Mignot; Jean-Philippe Jais; Chrystèle Bilhou-Nabéra; Despina Moshous; Bénédicte Neven; Capucine Picard; Geneviève de Saint-Basile; Marina Cavazzana-Calvo; Stéphane Blanche; Alain Fischer
Journal:  Blood       Date:  2012-12-20       Impact factor: 22.113

9.  PRKDC mutations in a SCID patient with profound neurological abnormalities.

Authors:  Lisa Woodbine; Jessica A Neal; Nanda-Kumar Sasi; Mayuko Shimada; Karen Deem; Helen Coleman; William B Dobyns; Tomoo Ogi; Katheryn Meek; E Graham Davies; Penny A Jeggo
Journal:  J Clin Invest       Date:  2013-06-03       Impact factor: 14.808

10.  Haemopoietic stem-cell transplantation with antibody-based minimal-intensity conditioning: a phase 1/2 study.

Authors:  Karin C Straathof; Kanchan Rao; Matthias Eyrich; Geoff Hale; Prudence Bird; Eleanor Berrie; Lucinda Brown; Stuart Adams; Paul G Schlegel; Nicholas Goulden; H Bobby Gaspar; Andrew R Gennery; Paul Landais; E G Davies; Malcolm K Brenner; Paul A Veys; Persis Jal Amrolia
Journal:  Lancet       Date:  2009-09-02       Impact factor: 79.321

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2.  Transplantation of Hematopoietic Stem Cells for Primary Immunodeficiencies in Brazil: Challenges in Treating Rare Diseases in Developing Countries.

Authors:  Juliana Folloni Fernandes; Samantha Nichele; Liane E Daudt; Rita B Tavares; Adriana Seber; Fábio R Kerbauy; Adriana Koliski; Gisele Loth; Ana K Vieira; Luiz G Darrigo-Junior; Vanderson Rocha; Alessandra A Gomes; Vergílio Colturato; Luiz F Mantovani; Andreza F Ribeiro; Lisandro L Ribeiro; Cilmara Kuwahara; Ana L M Rodrigues; Victor G Zecchin; Beatriz T Costa-Carvalho; Magda Carneiro-Sampaio; Antonio Condino-Neto; Anders Fasth; Andrew Gennery; Ricardo Pasquini; Nelson Hamerschlak; Carmem Bonfim
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3.  Utility of DNA, RNA, Protein, and Functional Approaches to Solve Cryptic Immunodeficiencies.

Authors:  Margot A Cousin; Matthew J Smith; Ashley N Sigafoos; Jay J Jin; Marine I Murphree; Nicole J Boczek; Patrick R Blackburn; Gavin R Oliver; Ross A Aleff; Karl J Clark; Eric D Wieben; Avni Y Joshi; Pavel N Pichurin; Roshini S Abraham; Eric W Klee
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Review 4.  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

5.  Prospective Study of a Cohort of Russian Nijmegen Breakage Syndrome Patients Demonstrating Predictive Value of Low Kappa-Deleting Recombination Excision Circle (KREC) Numbers and Beneficial Effect of Hematopoietic Stem Cell Transplantation (HSCT).

Authors:  Elena Deripapa; Dmitry Balashov; Yulia Rodina; Alexandra Laberko; Natalya Myakova; Nataliia V Davydova; Maria A Gordukova; Dmitrii S Abramov; Galina V Pay; Larisa Shelikhova; Andrey P Prodeus; Mikhail A Maschan; Alexey A Maschan; Anna Shcherbina
Journal:  Front Immunol       Date:  2017-07-24       Impact factor: 7.561

6.  Case Report: Refractory Cytopenia With a Switch From a Transient Monosomy 7 to a Disease-Ameliorating del(20q) in a NHEJ1-Deficient Long-term Survivor.

Authors:  Fiona Poyer; Raúl Jimenez Heredia; Wolfgang Novak; Petra Zeitlhofer; Karin Nebral; Michael N Dworzak; Oskar A Haas; Kaan Boztug; Leo Kager
Journal:  Front Immunol       Date:  2022-06-24       Impact factor: 8.786

7.  Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders.

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Review 8.  Treosulfan-based conditioning for inborn errors of immunity.

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9.  Survival and Functional Immune Reconstitution After Haploidentical Stem Cell Transplantation in Atm-Deficient Mice.

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Journal:  Mol Ther Methods Clin Dev       Date:  2021-05-05       Impact factor: 6.698

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