Literature DB >> 30772512

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

Madeleine Taylor1, Shaukat Khan2, Molly Stapleton1, Jianmin Wang3, Jing Chen3, Robert Wynn4, Hiromasa Yabe5, Yasutsugu Chinen6, Jaap Jan Boelens7, Robert W Mason1, Francyne Kubaski8, Dafne D G Horovitz9, Anneliese L Barth9, Marta Serafini10, Maria Ester Bernardo11, Hironori Kobayashi12, Kenji E Orii13, Yasuyuki Suzuki14, Tadao Orii13, Shunji Tomatsu15.   

Abstract

Allogenic hematopoietic stem cell transplantation (HSCT) has proven to be a viable treatment option for a selected group of patients with mucopolysaccharidoses (MPS), including those with MPS types I, II, IVA, VI, and VII. Early diagnosis and timely referral to an expert in MPS are critical, followed by a complete examination and evaluation by a multidisciplinary team, including a transplantation physician. Treatment recommendations for MPS are based on multiple biological, sociological, and financial factors, including type of MPS, clinical severity, prognosis, present clinical signs and symptoms (disease stage), age at onset, rate of progression, family factors and expectations, financial burden, feasibility, availability, risks and benefits of available therapies such as HSCT, enzyme replacement therapy (ERT), surgical interventions, and other supportive care. International collaboration and data review are critical to evaluating the therapeutic efficacy and adverse effects of HSCT for MPS. Collaborative efforts to assess HSCT for MPS have been ongoing since the first attempt at HSCT in a patient with MPS reported in 1981. The accumulation of data since then has made it possible to identify early outcomes (ie, transplantation outcomes) and long-term disease-specific outcomes resulting from HSCT. The recent identification of predictive factors and the development of innovative regimens have significantly improved the outcomes of both engraftment failure and transplantation-related mortality. Assessment of long-term outcomes has considered a variety of factors, including type of MPS, type of graft, age at transplantation, and stage of disease progression, among others. Studies on long-term outcomes are considered a key factor in the use of HSCT in patients with MPS. These studies have shown the effects and limitations of HSCT on improving disease manifestations and quality of life. In this review, we summarize the efficacy, side effects, risks, and cost of HSCT for each type of MPS.
Copyright © 2019 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Allogenic hematopoietic stem cell transplantation; Enzyme replacement therapy; Limitations; Mucopolysaccharidoses; Outcomes

Mesh:

Year:  2019        PMID: 30772512      PMCID: PMC6615945          DOI: 10.1016/j.bbmt.2019.02.012

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


  180 in total

1.  Combined Enzyme Replacement Therapy and Hematopoietic Stem Cell Transplantation in Mucopolysacharidosis Type VI.

Authors:  D Sillence; K Waters; S Donaldson; P J Shaw; C Ellaway
Journal:  JIMD Rep       Date:  2011-09-06

2.  Urinary glycosaminoglycan excretion quantified by an automated semimicro method in specimens conveniently transported from around the globe.

Authors:  Chester B Whitley; Richard C Spielmann; Gerrard Herro; Suzanne Severson Teragawa
Journal:  Mol Genet Metab       Date:  2002-01       Impact factor: 4.797

3.  Long-term outcome of Hurler syndrome patients after hematopoietic cell transplantation: an international multicenter study.

Authors:  Mieke Aldenhoven; Robert F Wynn; Paul J Orchard; Anne O'Meara; Paul Veys; Alain Fischer; Vassili Valayannopoulos; Benedicte Neven; Attilio Rovelli; Vinod K Prasad; Jakub Tolar; Heather Allewelt; Simon A Jones; Rossella Parini; Marleen Renard; Victoria Bordon; Nico M Wulffraat; Tom J de Koning; Elsa G Shapiro; Joanne Kurtzberg; Jaap Jan Boelens
Journal:  Blood       Date:  2015-01-26       Impact factor: 22.113

Review 4.  Allogeneic hematopoietic stem cell transplantation (HSCT) after reduced intensity conditioning.

Authors:  Sophie Servais; Frédéric Baron; Yves Beguin
Journal:  Transfus Apher Sci       Date:  2011-02-22       Impact factor: 1.764

5.  Cost structure and clinical outcome of a stem cell transplantation program in a developing country: the experience in northeast Mexico.

Authors:  José Carlos Jaime-Pérez; Alberto Carlos Heredia-Salazar; Olga G Cantú-Rodríguez; Homero Gutiérrez-Aguirre; César Daniel Villarreal-Villarreal; Consuelo Mancías-Guerra; José Luís Herrera-Garza; David Gómez-Almaguer
Journal:  Oncologist       Date:  2015-03-06

Review 6.  Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment.

Authors:  S Tomatsu; A M Montaño; H Oikawa; M Smith; L Barrera; Y Chinen; M M Thacker; W G Mackenzie; Y Suzuki; T Orii
Journal:  Curr Pharm Biotechnol       Date:  2011-06       Impact factor: 2.837

Review 7.  Mucopolysaccharidosis VI.

Authors:  Vassili Valayannopoulos; Helen Nicely; Paul Harmatz; Sean Turbeville
Journal:  Orphanet J Rare Dis       Date:  2010-04-12       Impact factor: 4.123

Review 8.  Allogeneic stem cell transplantation for the treatment of lysosomal and peroxisomal metabolic diseases.

Authors:  William Krivit
Journal:  Springer Semin Immunopathol       Date:  2004-09-25

9.  Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I.

Authors:  Lorne A Clarke; J Edmond Wraith; Michael Beck; Edwin H Kolodny; Gregory M Pastores; Joseph Muenzer; David M Rapoport; Kenneth I Berger; Marisa Sidman; Emil D Kakkis; Gerald F Cox
Journal:  Pediatrics       Date:  2009-01       Impact factor: 7.124

10.  Glycosaminoglycan storage disorders: a review.

Authors:  Maria Francisca Coutinho; Lúcia Lacerda; Sandra Alves
Journal:  Biochem Res Int       Date:  2011-10-05
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  48 in total

1.  A novel conditioning-free hematopoietic stem cell transplantation model in zebrafish.

Authors:  Ellen Fraint; María Feliz Norberto; Teresa V Bowman
Journal:  Blood Adv       Date:  2020-12-22

Review 2.  Gene therapy using haematopoietic stem and progenitor cells.

Authors:  Giuliana Ferrari; Adrian J Thrasher; Alessandro Aiuti
Journal:  Nat Rev Genet       Date:  2020-12-10       Impact factor: 53.242

Review 3.  Hurdles in treating Hurler disease: potential routes to achieve a "real" cure.

Authors:  Brigitte T A van den Broek; Jaap van Doorn; Charlotte V Hegeman; Stefan Nierkens; Caroline A Lindemans; Nanda Verhoeven-Duif; Jaap Jan Boelens; Peter M van Hasselt
Journal:  Blood Adv       Date:  2020-06-23

4.  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

5.  High-throughput analysis of hematopoietic stem cell engraftment after intravenous and intracerebroventricular dosing.

Authors:  Robert N Plasschaert; Mark P DeAndrade; Fritz Hull; Quoc Nguyen; Tara Peterson; Aimin Yan; Mariana Loperfido; Cristina Baricordi; Luigi Barbarossa; John K Yoon; Yildirim Dogan; Zeenath Unnisa; Jeffrey W Schindler; Niek P van Til; Luca Biasco; Chris Mason
Journal:  Mol Ther       Date:  2022-05-25       Impact factor: 12.910

6.  A Cure for Sanfilippo Syndrome? A Summary of Current Therapeutic Approaches and their Promise.

Authors:  Yewande Pearse; Michelina Iacovino
Journal:  Med Res Arch       Date:  2020-02-21

Review 7.  Systemic diseases and the cornea.

Authors:  Ruchi Shah; Cynthia Amador; Kati Tormanen; Sean Ghiam; Mehrnoosh Saghizadeh; Vaithi Arumugaswami; Ashok Kumar; Andrei A Kramerov; Alexander V Ljubimov
Journal:  Exp Eye Res       Date:  2021-01-21       Impact factor: 3.467

8.  Biochemical evaluation of intracerebroventricular rhNAGLU-IGF2 enzyme replacement therapy in neonatal mice with Sanfilippo B syndrome.

Authors:  Shih-Hsin Kan; Ibrahim Elsharkawi; Steven Q Le; Heather Prill; Linley Mangini; Jonathan D Cooper; Roger Lawrence; Mark S Sands; Brett E Crawford; Patricia I Dickson
Journal:  Mol Genet Metab       Date:  2021-03-31       Impact factor: 4.204

Review 9.  Therapeutic Options for Mucopolysaccharidoses: Current and Emerging Treatments.

Authors:  Kazuki Sawamoto; Molly Stapleton; Carlos J Alméciga-Díaz; Angela J Espejo-Mojica; Juan Camilo Losada; Diego A Suarez; Shunji Tomatsu
Journal:  Drugs       Date:  2019-07       Impact factor: 11.431

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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