Literature DB >> 29153844

Treatment of brain disease in the mucopolysaccharidoses.

Maurizio Scarpa1, Paul J Orchard2, Angela Schulz3, Patricia I Dickson4, Mark E Haskins5, Maria L Escolar6, Roberto Giugliani7.   

Abstract

The mucopolysaccharidosis (MPS) disorders are a group of lysosomal storage diseases caused by lysosomal enzyme deficits that lead to glycosaminoglycan accumulation, affecting various tissues throughout the body based on the specific enzyme deficiency. These disorders are characterized by their progressive nature and a variety of somatic manifestations and neurological symptoms. There are established treatments for some MPS disorders, but these mostly alleviate somatic and non-neurological symptoms and do not cure the disease. Patients with MPS I, II, III, and VII can present with neurological manifestations such as neurocognitive decline and behavioral problems. Treatment of these neurological manifestations remains challenging due to the blood-brain barrier (BBB) that limits delivery of therapeutic agents to the central nervous system (CNS). New therapies that circumvent this barrier and target brain disease in MPS are currently under development. They primarily focus on facilitating penetration of drugs through the BBB, delivery of recombinant enzyme to the brain by gene therapy, or direct CNS administration. This review summarizes existing and potential future treatment approaches that target brain disease in MPS. The information in this review is based on current literature and presentations and discussions during a closed meeting by an international group of experts with extensive experience in managing and treating MPS.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Blood-brain barrier; Enzyme replacement therapy; Gene therapy; Mucopolysaccharidoses; Transplantation

Mesh:

Substances:

Year:  2017        PMID: 29153844     DOI: 10.1016/j.ymgme.2017.10.007

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


  21 in total

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Authors:  Carlos R Ferreira; Debra S Regier; Robin Yoon; Kristen S Pan; Jean M Johnston; Sandra Yang; Jürgen W Spranger; Cynthia J Tifft
Journal:  Bone       Date:  2019-11-06       Impact factor: 4.398

Review 2.  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

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

Review 4.  Treatment of Neuronopathic Mucopolysaccharidoses with Blood-Brain Barrier-Crossing Enzymes: Clinical Application of Receptor-Mediated Transcytosis.

Authors:  Hiroyuki Sonoda; Kenichi Takahashi; Kohtaro Minami; Toru Hirato; Tatsuyoshi Yamamoto; Sairei So; Kazunori Tanizawa; Mathias Schmidt; Yuji Sato
Journal:  Pharmaceutics       Date:  2022-06-11       Impact factor: 6.525

Review 5.  Drug delivery for neuronopathic lysosomal storage diseases: evolving roles of the blood brain barrier and cerebrospinal fluid.

Authors:  Yuji Sato; Kohtaro Minami; Toru Hirato; Kazunori Tanizawa; Hiroyuki Sonoda; Mathias Schmidt
Journal:  Metab Brain Dis       Date:  2022-01-28       Impact factor: 3.655

6.  Characterization of Fluid Biomarkers Reveals Lysosome Dysfunction and Neurodegeneration in Neuronopathic MPS II Patients.

Authors:  Akhil Bhalla; Ritesh Ravi; Meng Fang; Annie Arguello; Sonnet S Davis; Chi-Lu Chiu; Jessica R Blumenfeld; Hoang N Nguyen; Timothy K Earr; Junhua Wang; Giuseppe Astarita; Yuda Zhu; Damian Fiore; Kimberly Scearce-Levie; Dolores Diaz; Heather Cahan; Matthew D Troyer; Jeffrey M Harris; Maria L Escolar
Journal:  Int J Mol Sci       Date:  2020-07-22       Impact factor: 5.923

7.  Temporospatial Development of Neuropathologic Findings in a Canine Model of Mucopolysaccharidosis IIIB.

Authors:  Tyler A Harm; Shannon J Hostetter; Ariel S Nenninger; Bethann N Valentine; N Matthew Ellinwood; Jodi D Smith
Journal:  Vet Pathol       Date:  2020-11-18       Impact factor: 2.221

Review 8.  Neurobehavioral phenotypes of neuronopathic mucopolysaccharidoses.

Authors:  Rita Barone; Alessandra Pellico; Annarita Pittalà; Serena Gasperini
Journal:  Ital J Pediatr       Date:  2018-11-16       Impact factor: 2.638

Review 9.  The Challenge of Modulating Heparan Sulfate Turnover by Multitarget Heparin Derivatives.

Authors:  Noemi Veraldi; Nawel Zouggari; Ariane de Agostini
Journal:  Molecules       Date:  2020-01-17       Impact factor: 4.411

10.  Brain Pathology in Mucopolysaccharidoses (MPS) Patients with Neurological Forms.

Authors:  Gustavo M Viana; David A Priestman; Frances M Platt; Shaukat Khan; Shunji Tomatsu; Alexey V Pshezhetsky
Journal:  J Clin Med       Date:  2020-02-01       Impact factor: 4.964

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