Literature DB >> 24100247

Enzyme augmentation therapy enhances the therapeutic efficacy of bone marrow transplantation in mucopolysaccharidosis type II mice.

Kazumasa Akiyama1, Yohta Shimada2, Takashi Higuchi2, Makoto Ohtsu3, Hiromitsu Nakauchi3, Hiroshi Kobayashi4, Takahiro Fukuda5, Hiroyuki Ida4, Yoshikatsu Eto6, Brett E Crawford7, Jillian R Brown7, Toya Ohashi8.   

Abstract

Before the availability of an enzyme replacement therapy (ERT) for mucopolysaccharidosis type II (MPS II), patients were treated by bone marrow transplantation (BMT). However, the effectiveness of BMT for MPS II was equivocal, particularly at addressing the CNS manifestations. To study this further, we subjected a murine model of MPS II to BMT and evaluated the effect at correcting the biochemical and pathological aberrations in the viscera and CNS. Our results indicated that BMT reduced the accumulation of glycosaminoglycans (GAGs) in a variety of visceral organs, but not in the CNS. With the availability of an approved ERT for MPS II, we investigated and compared the relative merits of the two strategies either as a mono or combination therapy. We showed that the combination of BMT and ERT was additive at reducing tissue levels of GAGs in the heart, kidney and lung. Moreover, ERT conferred greater efficacy if the immunological response against the infused recombinant enzyme was low. Finally, we showed that pathologic GAGs might potentially represent a sensitive biomarker to monitor the therapeutic efficacy of therapies for MPS II.
© 2013.

Entities:  

Keywords:  Bone marrow transplantation; Enzyme replacement therapy; Glycosaminoglycan; Hunter syndrome; Mucopolysaccharidosis; Pathologic glycosaminoglycan

Mesh:

Substances:

Year:  2013        PMID: 24100247     DOI: 10.1016/j.ymgme.2013.09.013

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  8 in total

1.  The efficacy of intracerebroventricular idursulfase-beta enzyme replacement therapy in mucopolysaccharidosis II murine model: heparan sulfate in cerebrospinal fluid as a clinical biomarker of neuropathology.

Authors:  Young Bae Sohn; Ah-Ra Ko; Mi-Ran Seong; Soyeon Lee; Mi Ra Kim; Sung Yoon Cho; Jung-Sun Kim; Makoto Sakaguchi; Takahiro Nakazawa; Motomichi Kosuga; Joo Hyun Seo; Torayuki Okuyama; Dong-Kyu Jin
Journal:  J Inherit Metab Dis       Date:  2018-07-05       Impact factor: 4.982

2.  Effect of donor chimerism to reduce the level of glycosaminoglycans following bone marrow transplantation in a murine model of mucopolysaccharidosis type II.

Authors:  Kentaro Yokoi; Kazumasa Akiyama; Eiko Kaneshiro; Takashi Higuchi; Yohta Shimada; Hiroshi Kobayashi; Masaharu Akiyama; Makoto Otsu; Hiromitsu Nakauchi; Toya Ohashi; Hiroyuki Ida
Journal:  J Inherit Metab Dis       Date:  2014-12-13       Impact factor: 4.982

3.  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

4.  Hematopoietic stem cell gene therapy ameliorates CNS involvement in murine model of GM1-gangliosidosis.

Authors:  Toshiki Tsunogai; Toya Ohashi; Yohta Shimada; Takashi Higuchi; Ayaka Kimura; Ayako M Watabe; Fusao Kato; Hiroyuki Ida; Hiroshi Kobayashi
Journal:  Mol Ther Methods Clin Dev       Date:  2022-04-28       Impact factor: 5.849

Review 5.  Failures of Endochondral Ossification in the Mucopolysaccharidoses.

Authors:  Zhirui Jiang; Sharon Byers; Margret L Casal; Lachlan J Smith
Journal:  Curr Osteoporos Rep       Date:  2020-10-16       Impact factor: 5.096

6.  Impact of Enzyme Replacement Therapy and Hematopoietic Stem Cell Therapy on Growth in Patients with Hunter Syndrome.

Authors:  Pravin Patel; Yasuyuki Suzuki; Akemi Tanaka; Hiromasa Yabe; Shunichi Kato; Tsutomu Shimada; Robert W Mason; Kenji E Orii; Toshiyuki Fukao; Tadao Orii; Shunji Tomatsu
Journal:  Mol Genet Metab Rep       Date:  2014

7.  Low-dose Gene Therapy Reduces the Frequency of Enzyme Replacement Therapy in a Mouse Model of Lysosomal Storage Disease.

Authors:  Marialuisa Alliegro; Rita Ferla; Edoardo Nusco; Chiara De Leonibus; Carmine Settembre; Alberto Auricchio
Journal:  Mol Ther       Date:  2016-09-23       Impact factor: 11.454

8.  Brain RNA-Seq Profiling of the Mucopolysaccharidosis Type II Mouse Model.

Authors:  Marika Salvalaio; Francesca D'Avanzo; Laura Rigon; Alessandra Zanetti; Michela D'Angelo; Giorgio Valle; Maurizio Scarpa; Rosella Tomanin
Journal:  Int J Mol Sci       Date:  2017-05-17       Impact factor: 5.923

  8 in total

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