Literature DB >> 28673849

Hematopoietic Stem Cell Transplantation for Patients with Mucopolysaccharidosis II.

Francyne Kubaski1, Hiromasa Yabe2, Yasuyuki Suzuki3, Toshiyuki Seto4, Takashi Hamazaki4, Robert W Mason5, Li Xie6, Tor Gunnar Hugo Onsten7, Sandra Leistner-Segal8, Roberto Giugliani9, Vũ Chí Dũng10, Can Thi Bich Ngoc10, Seiji Yamaguchi11, Adriana M Montaño12, Kenji E Orii13, Toshiyuki Fukao13, Haruo Shintaku4, Tadao Orii13, Shunji Tomatsu14.   

Abstract

There is limited information regarding the long-term outcomes of hematopoietic stem cell transplantation (HSCT) for mucopolysaccharidosis II (MPS II). In this study, clinical, biochemical, and radiologic findings were assessed in patients who underwent HSCT and/or enzyme replacement therapy (ERT). Demographic data for 146 HSCT patients were collected from 27 new cases and 119 published cases and were compared with 51 ERT and 15 untreated cases. Glycosaminoglycan (GAG) levels were analyzed by liquid chromatography tandem mass spectrometry in blood samples from HSCT, ERT, and untreated patients as well as age-matched controls. Long-term magnetic resonance imaging (MRI) findings were investigated in 13 treated patients (6 ERT and 7 HSCT). Mean age at HSCT was 5.5 years (range, 2 to 21.4 years) in new patients and 5.5 years (range, 10 months to 19.8 years) in published cases. None of the 27 new patients died as a direct result of the HSCT procedure. Graft-versus-host disease occurred in 8 (9%) out of 85 published cases, and 9 (8%) patients died from transplantation-associated complications. Most HSCT patients showed greater improvement in somatic features, joint movements, and activity of daily living than the ERT patients. GAG levels in blood were significantly reduced by ERT and levels were even lower after HSCT. HSCT patients showed either improvement or no progression of abnormal findings in brain MRI while abnormal findings became more extensive after ERT. HSCT seems to be more effective than ERT for MPS II in a wide range of disease manifestations and could be considered as a treatment option for this condition.
Copyright © 2017 The American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Enzyme replacement therapy; Hematopoietic stem cell transplantation; Hunter syndrome; Iduronate-2-sulfatase; Mucopolysaccharidosis II

Mesh:

Substances:

Year:  2017        PMID: 28673849      PMCID: PMC5659208          DOI: 10.1016/j.bbmt.2017.06.020

Source DB:  PubMed          Journal:  Biol Blood Marrow Transplant        ISSN: 1083-8791            Impact factor:   5.742


  51 in total

1.  Clinical outcomes following hematopoietic stem cell transplantation for the treatment of mucopolysaccharidosis VI.

Authors:  Sean Turbeville; Helen Nicely; J Douglas Rizzo; Tanya L Pedersen; Paul J Orchard; Mitchell E Horwitz; Edwin M Horwitz; Paul Veys; Carmem Bonfim; Amal Al-Seraihy
Journal:  Mol Genet Metab       Date:  2010-10-25       Impact factor: 4.797

Review 2.  Therapy for the mucopolysaccharidoses.

Authors:  Vassili Valayannopoulos; Frits A Wijburg
Journal:  Rheumatology (Oxford)       Date:  2011-12       Impact factor: 7.580

3.  Treatment of MPS VII (Sly disease) by allogeneic BMT in a female with homozygous A619V mutation.

Authors:  Y Yamada; K Kato; K Sukegawa; S Tomatsu; S Fukuda; S Emura; S Kojima; T Matsuyama; W S Sly; N Kondo; T Orii
Journal:  Bone Marrow Transplant       Date:  1998-03       Impact factor: 5.483

4.  Newborn screening for mucopolysaccharidoses: a pilot study of measurement of glycosaminoglycans by tandem mass spectrometry.

Authors:  Francyne Kubaski; Robert W Mason; Akiko Nakatomi; Haruo Shintaku; Li Xie; Naomi N van Vlies; Heather Church; Roberto Giugliani; Hironori Kobayashi; Seiji Yamaguchi; Yasuyuki Suzuki; Tadao Orii; Toshiyuki Fukao; Adriana M Montaño; Shunji Tomatsu
Journal:  J Inherit Metab Dis       Date:  2016-10-07       Impact factor: 4.982

5.  Umbilical cord-blood transplantations from unrelated donors in patients with inherited metabolic diseases: Single-institute experience.

Authors:  Sadao Tokimasa; Hideaki Ohta; Sachiko Takizawa; Shigenori Kusuki; Yoshiko Hashii; Norio Sakai; Masako Taniike; Keiichi Ozono; Junichi Hara
Journal:  Pediatr Transplant       Date:  2008-09

Review 6.  Long-term follow-up of a patient transplanted for Hunter's disease type IIB: a case report and literature review.

Authors:  S K Bergstrom; J J Quinn; R Greenstein; J Ascensao
Journal:  Bone Marrow Transplant       Date:  1994-10       Impact factor: 5.483

Review 7.  Cord blood and bone marrow transplantation in inherited metabolic diseases: scientific basis, current status and future directions.

Authors:  Vinod K Prasad; Joanne Kurtzberg
Journal:  Br J Haematol       Date:  2009-11-16       Impact factor: 6.998

8.  Bone marrow transplantation in children with Hunter syndrome: outcome after 7 to 17 years.

Authors:  Nathalie Guffon; Yves Bertrand; Isabelle Forest; Alain Fouilhoux; Roseline Froissart
Journal:  J Pediatr       Date:  2009-01-23       Impact factor: 4.406

9.  Localized donor cells in brain of a Hunter disease patient after cord blood stem cell transplantation.

Authors:  Ken Araya; Norio Sakai; Ikuko Mohri; Kuriko Kagitani-Shimono; Takeshi Okinaga; Yoshiko Hashii; Hideaki Ohta; Itsuko Nakamichi; Katsuyuki Aozasa; Masako Taniike; Keiichi Ozono
Journal:  Mol Genet Metab       Date:  2009-05-24       Impact factor: 4.797

Review 10.  Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy.

Authors:  J Edmond Wraith; Maurizio Scarpa; Michael Beck; Olaf A Bodamer; Linda De Meirleir; Nathalie Guffon; Allan Meldgaard Lund; Gunilla Malm; Ans T Van der Ploeg; Jiri Zeman
Journal:  Eur J Pediatr       Date:  2007-11-23       Impact factor: 3.183

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  37 in total

Review 1.  Lysosomal storage disease overview.

Authors:  Angela Sun
Journal:  Ann Transl Med       Date:  2018-12

Review 2.  Hematopoietic Stem Cell Transplantation for Mucopolysaccharidoses: Past, Present, and Future.

Authors:  Madeleine Taylor; Shaukat Khan; Molly Stapleton; Jianmin Wang; Jing Chen; Robert Wynn; Hiromasa Yabe; Yasutsugu Chinen; Jaap Jan Boelens; Robert W Mason; Francyne Kubaski; Dafne D G Horovitz; Anneliese L Barth; Marta Serafini; Maria Ester Bernardo; Hironori Kobayashi; Kenji E Orii; Yasuyuki Suzuki; Tadao Orii; Shunji Tomatsu
Journal:  Biol Blood Marrow Transplant       Date:  2019-02-14       Impact factor: 5.742

Review 3.  Newborn screening of mucopolysaccharidoses: past, present, and future.

Authors:  Nivethitha Arunkumar; Thomas J Langan; Molly Stapleton; Francyne Kubaski; Robert W Mason; Rajendra Singh; Hironori Kobayashi; Seiji Yamaguchi; Yasuyuki Suzuki; Kenji Orii; Tadao Orii; Toshiyuki Fukao; Shunji Tomatsu
Journal:  J Hum Genet       Date:  2020-04-10       Impact factor: 3.172

Review 4.  Gene therapy for Mucopolysaccharidoses.

Authors:  Kazuki Sawamoto; Hui-Hsuan Chen; Carlos J Alméciga-Díaz; Robert W Mason; Shunji Tomatsu
Journal:  Mol Genet Metab       Date:  2017-12-26       Impact factor: 4.797

Review 5.  Enzyme replacement therapy for mucopolysaccharidoses; past, present, and future.

Authors:  Hui Hsuan Chen; Kazuki Sawamoto; Robert W Mason; Hironori Kobayashi; Seiji Yamaguchi; Yasuyuki Suzuki; Kenji Orii; Tadao Orii; Shunji Tomatsu
Journal:  J Hum Genet       Date:  2019-08-27       Impact factor: 3.172

Review 6.  Allogeneic hematopoietic stem cell transplantation for inherited metabolic disorders.

Authors:  Hiromasa Yabe
Journal:  Int J Hematol       Date:  2022-05-20       Impact factor: 2.490

7.  A novel preclinical model of mucopolysaccharidosis type II for developing human hematopoietic stem cell gene therapy.

Authors:  Yohta Shimada; Natsumi Ishii; Takashi Higuchi; Motohito Goto; Toya Ohashi; Hiroshi Kobayashi
Journal:  Gene Ther       Date:  2022-07-14       Impact factor: 4.184

Review 8.  Recent trends in mucopolysaccharidosis research.

Authors:  Hiroshi Kobayashi
Journal:  J Hum Genet       Date:  2018-11-19       Impact factor: 3.172

9.  Umbilical mesenchymal stem cell-derived extracellular vesicles as enzyme delivery vehicle to treat Morquio A fibroblasts.

Authors:  Michael Flanagan; Isha Pathak; Qi Gan; Linda Winter; Ryan Emnet; Salem Akel; Adriana M Montaño
Journal:  Stem Cell Res Ther       Date:  2021-05-06       Impact factor: 6.832

10.  Therapy-type related long-term outcomes in mucopolysaccaridosis type II (Hunter syndrome) - Case series.

Authors:  Mojca Zerjav Tansek; Jana Kodric; Simona Klemencic; Jaap Jan Boelens; Peter M van Hasselt; Ana Drole Torkar; Maja Doric; Alenka Koren; Simona Avcin; Tadej Battelino; Urh Groselj
Journal:  Mol Genet Metab Rep       Date:  2021-06-26
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