Literature DB >> 30391550

Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency.

Susanne E Aydin1, Alexandra F Freeman2, Waleed Al-Herz3, Hamoud A Al-Mousa4, Rand K Arnaout5, Roland C Aydin1, Vincent Barlogis6, Bernd H Belohradsky7, Carmem Bonfim8, Robbert G Bredius9, Julia I Chu10, Oana C Ciocarlie11, Figen Doğu12, Hubert B Gaspar13, Raif S Geha14, Andrew R Gennery15, Fabian Hauck1, Abbas Hawwari16, Dennis D Hickstein17, Manfred Hoenig18, Aydan Ikinciogullari12, Christoph Klein1, Ashish Kumar19, Marianne R S Ifversen20, Susanne Matthes21, Ayse Metin22, Benedicte Neven23, Sung-Yun Pai24, Suhag H Parikh25, Capucine Picard26, Ellen D Renner27, Özden Sanal28, Ansgar S Schulz18, Friedhelm Schuster29, Nirali N Shah30, Evan B Shereck31, Mary A Slatter32, Helen C Su33, Joris van Montfrans34, Wilhelm Woessmann35, John B Ziegler36, Michael H Albert37.   

Abstract

BACKGROUND: Biallelic variations in the dedicator of cytokinesis 8 (DOCK8) gene cause a combined immunodeficiency with eczema, recurrent bacterial and viral infections, and malignancy. Natural disease outcome is dismal, but allogeneic hematopoietic stem cell transplantation (HSCT) can cure the disease.
OBJECTIVE: To determine outcome of HSCT for DOCK8 deficiency and define possible outcome variables.
METHODS: We performed a retrospective study of the results of HSCT in a large international cohort of DOCK8-deficient patients.
RESULTS: We identified 81 patients from 22 centers transplanted at a median age of 9.7 years (range, 0.7-27.2 years) between 1995 and 2015. After median follow-up of 26 months (range, 3-135 months), 68 (84%) patients are alive. Severe acute (III-IV) or chronic graft versus host disease occurred in 11% and 10%, respectively. Causes of death were infections (n = 5), graft versus host disease (5), multiorgan failure (2), and preexistent lymphoma (1). Survival after matched related (n = 40) or unrelated (35) HSCT was 89% and 81%, respectively. Reduced-toxicity conditioning based on either treosulfan or reduced-dose busulfan resulted in superior survival compared with fully myeloablative busulfan-based regimens (97% vs 78%; P = .049). Ninety-six percent of patients younger than 8 years at HSCT survived, compared with 78% of those 8 years and older (P = .06). Of the 73 patients with chimerism data available, 65 (89%) had more than 90% donor T-cell chimerism at last follow-up. Not all disease manifestations responded equally well to HSCT: eczema, infections, and mollusca resolved quicker than food allergies or failure to thrive.
CONCLUSIONS: HSCT is curative in most DOCK8-deficient patients, confirming this approach as the treatment of choice. HSCT using a reduced-toxicity regimen may offer the best chance for survival.
Copyright © 2018. Published by Elsevier Inc.

Entities:  

Keywords:  Combined immunodeficiency; DOCK8 deficiency; HSCT

Mesh:

Substances:

Year:  2018        PMID: 30391550      PMCID: PMC6771433          DOI: 10.1016/j.jaip.2018.10.035

Source DB:  PubMed          Journal:  J Allergy Clin Immunol Pract


  24 in total

1.  Successful allogeneic hematopoietic stem cell transplantation for DOCK8 deficiency.

Authors:  Vincent Barlogis; Claire Galambrun; Hervé Chambost; Sylvie Lamoureux-Toth; Philippe Petit; Jean-Louis Stephan; Gérard Michel; Alain Fischer; Capucine Picard
Journal:  J Allergy Clin Immunol       Date:  2011-05-04       Impact factor: 10.793

2.  Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation.

Authors:  S A Gatz; U Benninghoff; C Schütz; A Schulz; M Hönig; U Pannicke; K-H Holzmann; K Schwarz; W Friedrich
Journal:  Bone Marrow Transplant       Date:  2010-07-12       Impact factor: 5.483

3.  In DOCK8 deficiency donor cell engraftment post-genoidentical hematopoietic stem cell transplantation is possible without conditioning.

Authors:  Hamoud Al-Mousa; Abbas Hawwari; Zobaida Alsum
Journal:  J Allergy Clin Immunol       Date:  2013-01-23       Impact factor: 10.793

4.  Haploidentical stem cell transplantation in DOCK8 deficiency - Successful control of pre-existing severe viremia with a TCRaß/CD19-depleted graft and antiviral treatment.

Authors:  Sujal Ghosh; Friedhelm R Schuster; Ortwin Adams; Florian Babor; Arndt Borkhardt; Patrizia Comoli; Rupert Handgretinger; Peter Lang; Hans-Jürgen Laws; Meinolf Siepermann; Roland Meisel
Journal:  Clin Immunol       Date:  2014-03-22       Impact factor: 3.969

5.  Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantation.

Authors:  T C Bittner; U Pannicke; E D Renner; G Notheis; F Hoffmann; B H Belohradsky; U Wintergerst; M Hauser; B Klein; K Schwarz; I Schmid; M H Albert
Journal:  Klin Padiatr       Date:  2010-11-05       Impact factor: 1.349

6.  Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomal-recessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency.

Authors:  Douglas R McDonald; Michel J Massaad; Alicia Johnston; Sevgi Keles; Talal Chatila; Raif S Geha; Sung-Yun Pai
Journal:  J Allergy Clin Immunol       Date:  2010-12       Impact factor: 10.793

7.  Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen.

Authors:  Heidrun Boztug; Cäcilia Karitnig-Weiß; Bernd Ausserer; Ellen D Renner; Michael H Albert; Julie Sawalle-Belohradsky; Bernd H Belohradsky; Georg Mann; Ernst Horcher; Alexandra Rümmele-Waibel; Rene Geyeregger; Karoly Lakatos; Christina Peters; Anita Lawitschka; Susanne Matthes-Martin
Journal:  Pediatr Hematol Oncol       Date:  2012-08-16       Impact factor: 1.969

8.  Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.

Authors:  Karin R Engelhardt; Sean McGhee; Sabine Winkler; Atfa Sassi; Cristina Woellner; Gabriela Lopez-Herrera; Andrew Chen; Hong Sook Kim; Maria Garcia Lloret; Ilka Schulze; Stephan Ehl; Jens Thiel; Dietmar Pfeifer; Hendrik Veelken; Tim Niehues; Kathrin Siepermann; Sebastian Weinspach; Ismail Reisli; Sevgi Keles; Ferah Genel; Necil Kutukculer; Necil Kutuculer; Yildiz Camcioğlu; Ayper Somer; Elif Karakoc-Aydiner; Isil Barlan; Andrew Gennery; Ayse Metin; Aydan Degerliyurt; Maria C Pietrogrande; Mehdi Yeganeh; Zeina Baz; Salem Al-Tamemi; Christoph Klein; Jennifer M Puck; Steven M Holland; Edward R B McCabe; Bodo Grimbacher; Talal A Chatila
Journal:  J Allergy Clin Immunol       Date:  2009-12       Impact factor: 10.793

9.  Combined immunodeficiency associated with DOCK8 mutations.

Authors:  Qian Zhang; Jeremiah C Davis; Ian T Lamborn; Alexandra F Freeman; Huie Jing; Amanda J Favreau; Helen F Matthews; Joie Davis; Maria L Turner; Gulbu Uzel; Steven M Holland; Helen C Su
Journal:  N Engl J Med       Date:  2009-09-23       Impact factor: 91.245

10.  Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity.

Authors:  Eleonore D Renner; Jennifer M Puck; Steven M Holland; Markus Schmitt; Michael Weiss; Michael Frosch; Markus Bergmann; Joie Davis; Bernd H Belohradsky; Bodo Grimbacher
Journal:  J Pediatr       Date:  2004-01       Impact factor: 4.406

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  18 in total

1.  Hematopoietic stem cell transplant effectively rescues lymphocyte differentiation and function in DOCK8-deficient patients.

Authors:  Bethany A Pillay; Danielle T Avery; Joanne M Smart; Theresa Cole; Sharon Choo; Damien Chan; Paul E Gray; Katie Frith; Richard Mitchell; Tri Giang Phan; Melanie Wong; Dianne E Campbell; Peter Hsu; John B Ziegler; Jane Peake; Frank Alvaro; Capucine Picard; Jacinta Bustamante; Benedicte Neven; Andrew J Cant; Gulbu Uzel; Peter D Arkwright; Jean-Laurent Casanova; Helen C Su; Alexandra F Freeman; Nirali Shah; Dennis D Hickstein; Stuart G Tangye; Cindy S Ma
Journal:  JCI Insight       Date:  2019-04-25

2.  Allogeneic hematopoietic stem cell transplantation in leukocyte adhesion deficiency type I and III.

Authors:  Shahrzad Bakhtiar; Emilia Salzmann-Manrique; Henric-Jan Blok; Dirk-Jan Eikema; Sheree Hazelaar; Mouhab Ayas; Amos Toren; Gal Goldstein; Despina Moshous; Franco Locatelli; Pietro Merli; Gerard Michel; Gülyüz Öztürk; Ansgar Schulz; Carsten Heilmann; Marianne Ifversen; Rob F Wynn; Olga Aleinikova; Yves Bertrand; Abdelghani Tbakhi; Paul Veys; Musa Karakukcu; Alphan Kupesiz; Ardeshir Ghavamzadeh; Rupert Handgretinger; Emel Unal; Antonio Perez-Martinez; Muge Gokce; Fulvio Porta; Tekin Aksu; Gülsün Karasu; Isabel Badell; Per Ljungman; Elena Skorobogatova; Akif Yesilipek; Tsila Zuckerman; Robbert R G Bredius; Polina Stepensky; Bella Shadur; Mary Slatter; Andrew R Gennery; Michael H Albert; Peter Bader; Arjan Lankester
Journal:  Blood Adv       Date:  2021-01-12

3.  Cryptosporidium infection in dedicator of cytokinesis 8 (DOCK 8) deficiency.

Authors:  Gil Ben Yakov; Disha Sharma; Min H Cho; Nirali N Shah; Dennis Hickstein; Amanda Urban; Dirk Darnell; Devika Kapuria; Jamie Marko; David E Kleiner; Colleen M Hadigan; Jeffrey Danielson; Hyoungjun Ham; Anusha Vittal; Helen C Su; Alexandra F Freeman; Theo Heller
Journal:  J Allergy Clin Immunol Pract       Date:  2020-06-22

4.  Compound Heterozygous DOCK8 Mutations in a Patient with B Lymphoblastic Leukemia and EBV-Associated Diffuse Large B Cell Lymphoma.

Authors:  David Buchbinder; Ivan Kirov; Jeffrey Danielson; Nirali N Shah; Alexandra F Freeman; Rishikesh S Chavan; Helen C Su
Journal:  J Clin Immunol       Date:  2019-07-02       Impact factor: 8.317

5.  Recalcitrant Warts, Epidermodysplasia Verruciformis, and the Tree-Man Syndrome: Phenotypic Spectrum of Cutaneous Human Papillomavirus Infections at the Intersection of Genetic Variability of Viral and Human Genomes.

Authors:  Jouni Uitto; Amir Hossein Saeidian; Leila Youssefian; Zahra Saffarian; Jean-Laurent Casanova; Vivien Béziat; Emmanuelle Jouanguy; Hassan Vahidnezhad
Journal:  J Invest Dermatol       Date:  2021-11-27       Impact factor: 7.590

6.  Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8.

Authors:  Paul E Gray; Bethany A Pillay; Stuart G Tangye; Jin Yan Yap; William A Figgett; John Reeves; Sarah K Kummerfeld; Jennifer Stoddard; Gulbu Uzel; Huie Jing; Helen C Su; Dianne E Campbell; Anna Sullivan; Leslie Burnett; Jane Peake; Cindy S Ma
Journal:  J Clin Immunol       Date:  2021-10-17       Impact factor: 8.542

Review 7.  Inborn errors of immunity with atopic phenotypes: A practical guide for allergists.

Authors:  Riccardo Castagnoli; Vassilios Lougaris; Giuliana Giardino; Stefano Volpi; Lucia Leonardi; Francesco La Torre; Silvia Federici; Stefania Corrente; Bianca Laura Cinicola; Annarosa Soresina; Caterina Cancrini; Gian Luigi Marseglia; Fabio Cardinale
Journal:  World Allergy Organ J       Date:  2021-02-22       Impact factor: 4.084

Review 8.  Considerations for hematopoietic stem cell transplantation in primary immunodeficiency disorders.

Authors:  Tatyana Gavrilova
Journal:  World J Transplant       Date:  2019-07-31

Review 9.  Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Diseases: Current Status and Future Perspectives.

Authors:  Riccardo Castagnoli; Ottavia Maria Delmonte; Enrica Calzoni; Luigi Daniele Notarangelo
Journal:  Front Pediatr       Date:  2019-08-08       Impact factor: 3.418

10.  The paradigm of hematological malignant versus non-malignant manifestations, driven by primary immunodeficiencies: a complex interplay.

Authors:  C Kelaidi; V Tzotzola; S Polychronopoulou
Journal:  Fam Cancer       Date:  2021-06-15       Impact factor: 2.375

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