Literature DB >> 23131490

Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes.

Rebecca A Marsh1, Kanchan Rao, Prakash Satwani, Kai Lehmberg, Ingo Müller, Dandan Li, Mi-Ok Kim, Alain Fischer, Sylvain Latour, Petr Sedlacek, Vincent Barlogis, Kazuko Hamamoto, Hirokazu Kanegane, Sam Milanovich, David A Margolis, David Dimmock, James Casper, Dorothea N Douglas, Persis J Amrolia, Paul Veys, Ashish R Kumar, Michael B Jordan, Jack J Bleesing, Alexandra H Filipovich.   

Abstract

There have been no studies on patient outcome after allogeneic hematopoietic cell transplantation (HCT) in patients with X-linked inhibitor of apoptosis (XIAP) deficiency. To estimate the success of HCT, we conducted an international survey of transplantation outcomes. Data were reported for 19 patients. Seven patients received busulfan-containing myeloablative conditioning (MAC) regimens. Eleven patients underwent reduced intensity conditioning (RIC) regimens predominantly consisting of alemtuzumab, fludarabine, and melphalan. One patient received an intermediate-intensity regimen. Survival was poor in the MAC group, with only 1 patient surviving (14%). Most deaths were from transplantation-related toxicities, including venoocclusive disease and pulmonary hemorrhage. Of the 11 patients who received RIC, 6 are currently surviving at a median of 570 days after HCT (55%). Preparative regimen and HLH activity affected outcomes, and of RIC patients reported to be in remission from HLH, survival is 86% (P = .03). We conclude that MAC regimens should not be used for patients with XIAP deficiency. It is possible that the loss of XIAP and its antiapoptotic functions contributes to the high incidence of toxicities observed with MAC regimens. RIC regimens should be pursued with caution and, if possible, efforts should be made to ensure HLH remission before HCT in these patients.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 23131490      PMCID: PMC5162550          DOI: 10.1182/blood-2012-06-432500

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  30 in total

1.  A conserved family of cellular genes related to the baculovirus iap gene and encoding apoptosis inhibitors.

Authors:  C S Duckett; V E Nava; R W Gedrich; R J Clem; J L Van Dongen; M C Gilfillan; H Shiels; J M Hardwick; C B Thompson
Journal:  EMBO J       Date:  1996-06-03       Impact factor: 11.598

2.  XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease.

Authors:  Rebecca A Marsh; Lisa Madden; Brenda J Kitchen; Rajen Mody; Brad McClimon; Michael B Jordan; Jack J Bleesing; Kejian Zhang; Alexandra H Filipovich
Journal:  Blood       Date:  2010-05-20       Impact factor: 22.113

3.  Clinical features and outcome of X-linked lymphoproliferative syndrome type 1 (SAP deficiency) in Japan identified by the combination of flow cytometric assay and genetic analysis.

Authors:  Hirokazu Kanegane; Xi Yang; Meina Zhao; Kazumi Yamato; Masami Inoue; Kazuko Hamamoto; Chie Kobayashi; Ako Hosono; Yoshikiyo Ito; Yozo Nakazawa; Kiminori Terui; Kazuhiro Kogawa; Eiichi Ishii; Ryo Sumazaki; Toshio Miyawaki
Journal:  Pediatr Allergy Immunol       Date:  2012-03-21       Impact factor: 6.377

4.  Allogeneic stem cell transplantation in X-linked lymphoproliferative disease: two cases in one family and review of the literature.

Authors:  A C Lankester; L F A Visser; N G Hartwig; R G M Bredius; H B Gaspar; M van der Burg; M J D van Tol; T G Gross; R M Egeler
Journal:  Bone Marrow Transplant       Date:  2005-07       Impact factor: 5.483

Review 5.  The impact of HLA genotyping on survival following unrelated donor haematopoietic stem cell transplantation.

Authors:  Bronwen E Shaw; Rafael Arguello; Christian A Garcia-Sepulveda; J Alejandro Madrigal
Journal:  Br J Haematol       Date:  2010-06-15       Impact factor: 6.998

6.  Reduced-intensity conditioning significantly improves survival of patients with hemophagocytic lymphohistiocytosis undergoing allogeneic hematopoietic cell transplantation.

Authors:  Rebecca A Marsh; Gretchen Vaughn; Mi-Ok Kim; Dandan Li; Sonata Jodele; Sarita Joshi; Parinda A Mehta; Stella M Davies; Michael B Jordan; Jack J Bleesing; Alexandra H Filipovich
Journal:  Blood       Date:  2010-09-20       Impact factor: 22.113

7.  Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

Authors:  Annacarin Horne; Gritta Janka; R Maarten Egeler; Helmut Gadner; Shinsaku Imashuku; Stephan Ladisch; Franco Locatelli; Scott M Montgomery; David Webb; Jacek Winiarski; Alexandra H Filipovich; Jan-Inge Henter
Journal:  Br J Haematol       Date:  2005-06       Impact factor: 6.998

8.  A rapid flow cytometric screening test for X-linked lymphoproliferative disease due to XIAP deficiency.

Authors:  Rebecca A Marsh; Joyce Villanueva; Kejian Zhang; Andrew L Snow; Helen C Su; Lisa Madden; Rajen Mody; Brenda Kitchen; Dan Marmer; Michael B Jordan; Kimberly A Risma; Alexandra H Filipovich; Jack J Bleesing
Journal:  Cytometry B Clin Cytom       Date:  2009-09       Impact factor: 3.058

9.  Hematopoietic stem cell transplantation for familial hemophagocytic lymphohistiocytosis and Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in Japan.

Authors:  Shouichi Ohga; Kazuko Kudo; Eiichi Ishii; Satoshi Honjo; Akira Morimoto; Yuko Osugi; Akihisa Sawada; Masami Inoue; Ken Tabuchi; Nobuhiro Suzuki; Yasushi Ishida; Shinsaku Imashuku; Shunichi Kato; Toshiro Hara
Journal:  Pediatr Blood Cancer       Date:  2010-02       Impact factor: 3.167

Review 10.  Diagnosis and manifestations of chronic graft-versus-host disease.

Authors:  Alexandra H Filipovich
Journal:  Best Pract Res Clin Haematol       Date:  2008-06       Impact factor: 3.020

View more
  45 in total

1.  Nucleotide-binding oligomerization domain (NOD) signaling defects and cell death susceptibility cannot be uncoupled in X-linked inhibitor of apoptosis (XIAP)-driven inflammatory disease.

Authors:  Steven M Chirieleison; Rebecca A Marsh; Prathna Kumar; Joseph K Rathkey; George R Dubyak; Derek W Abbott
Journal:  J Biol Chem       Date:  2017-04-12       Impact factor: 5.157

2.  Risk-factors Associated With Poor Outcomes in VEO-IBD Secondary to XIAP Deficiency: A Case Report and Literature Review.

Authors:  Asama Lekbua; Jodie Ouahed; Amy E O'Connell; Stacy A Kahn; Jeffrey D Goldsmith; Toshihiko Imamura; Christine N Duncan; Judith R Kelsen; Elizabeth Worthey; Scott B Snapper; Samir Softic
Journal:  J Pediatr Gastroenterol Nutr       Date:  2019-07       Impact factor: 2.839

Review 3.  The Treatment of Inflammatory Bowel Disease in Patients with Selected Primary Immunodeficiencies.

Authors:  Dror S Shouval; Matthew Kowalik; Scott B Snapper
Journal:  J Clin Immunol       Date:  2018-06-29       Impact factor: 8.317

4.  IFNɣ Block, Treosulfan Conditioning and αβ T Cell Deplete PBSCT for XIAP-Deficient HLH.

Authors:  Ciara O'Rafferty; Mark Velangi; Sarah Lawson; Prashant Hiwarkar; Jayashree Motwani
Journal:  J Clin Immunol       Date:  2017-06-21       Impact factor: 8.317

5.  A critical role for cellular inhibitor of protein 2 (cIAP2) in colitis-associated colorectal cancer and intestinal homeostasis mediated by the inflammasome and survival pathways.

Authors:  M Dagenais; J Dupaul-Chicoine; C Champagne; A Skeldon; A Morizot; M Saleh
Journal:  Mucosal Immunol       Date:  2015-06-03       Impact factor: 7.313

6.  BIRC4 Mutation: An Important Rare Cause of Uveitis.

Authors:  Matthew L Basiaga; Pamela F Weiss; Edward M Behrens
Journal:  J Clin Rheumatol       Date:  2015-12       Impact factor: 3.517

Review 7.  Hemophagocytic Syndrome and Critical Illness: New Insights into Diagnosis and Management.

Authors:  Zuzana Tothova; Nancy Berliner
Journal:  J Intensive Care Med       Date:  2014-01-08       Impact factor: 3.510

8.  IAPs protect host target tissues from graft-versus-host disease in mice.

Authors:  Tomomi Toubai; Corinne Rossi; Katherine Oravecz-Wilson; Chen Liu; Cynthia Zajac; Shin-Rong Julia Wu; Yaping Sun; Hideaki Fujiwara; Hiroya Tamaki; Daniel Peltier; Mary Riwes; Israel Henig; Stuart Brabbs; Colin S Duckett; Shaomeng Wang; Pavan Reddy
Journal:  Blood Adv       Date:  2017-08-16

9.  Targeted busulfan-based reduced-intensity conditioning and HLA-matched HSCT cure hemophagocytic lymphohistiocytosis.

Authors:  Matthias Felber; Colin G Steward; Karim Kentouche; Anders Fasth; Robert F Wynn; Ulrike Zeilhofer; Veronika Haunerdinger; Benjamin Volkmer; Seraina Prader; Bernd Gruhn; Stephan Ehl; Kai Lehmberg; Daniel Müller; Andrew R Gennery; Michael H Albert; Fabian Hauck; Kanchan Rao; Paul Veys; Moustapha Hassan; Arjan C Lankester; Jana Pachlopnik Schmid; Mathias M Hauri-Hohl; Tayfun Güngör
Journal:  Blood Adv       Date:  2020-05-12

10.  The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosis.

Authors:  Bernd Hartz; Rebecca Marsh; Kanchan Rao; Jan-Inge Henter; Michael Jordan; Lisa Filipovich; Peter Bader; Rita Beier; Birgit Burkhardt; Roland Meisel; Ansgar Schulz; Beate Winkler; Michael H Albert; Johann Greil; Gülsün Karasu; Wilhelm Woessmann; Selim Corbacioglu; Bernd Gruhn; Wolfgang Holter; Jörn-Sven Kühl; Peter Lang; Markus G Seidel; Paul Veys; Alexandra Löfstedt; Sandra Ammann; Stephan Ehl; Gritta Janka; Ingo Müller; Kai Lehmberg
Journal:  Blood       Date:  2016-04-20       Impact factor: 22.113

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.