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Pentosan Polysulfate: A Novel Therapy for the Mucopolysaccharidoses

BACKGROUND: Pentosan polysulfate (PPS) is an FDA-approved, oral medication with anti-inflammatory and pro-chondrogenic properties. We have previously shown that animal models of the mucopolysaccharidoses (MPS) exhibit significant inflammatory disease, contributing to cartilage degeneration. Enzyme r...

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Autores principales: Schuchman, Edward H., Ge, Yi, Lai, Alon, Borisov, Yury, Faillace, Meghan, Eliyahu, Efrat, He, Xingxuan, Iatridis, James, Vlassara, Helen, Striker, Gary, Simonaro, Calogera M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554761/
https://www.ncbi.nlm.nih.gov/pubmed/23365668
http://dx.doi.org/10.1371/journal.pone.0054459
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author Schuchman, Edward H.
Ge, Yi
Lai, Alon
Borisov, Yury
Faillace, Meghan
Eliyahu, Efrat
He, Xingxuan
Iatridis, James
Vlassara, Helen
Striker, Gary
Simonaro, Calogera M.
author_facet Schuchman, Edward H.
Ge, Yi
Lai, Alon
Borisov, Yury
Faillace, Meghan
Eliyahu, Efrat
He, Xingxuan
Iatridis, James
Vlassara, Helen
Striker, Gary
Simonaro, Calogera M.
author_sort Schuchman, Edward H.
collection PubMed
description BACKGROUND: Pentosan polysulfate (PPS) is an FDA-approved, oral medication with anti-inflammatory and pro-chondrogenic properties. We have previously shown that animal models of the mucopolysaccharidoses (MPS) exhibit significant inflammatory disease, contributing to cartilage degeneration. Enzyme replacement therapy (ERT) only partly reduced inflammation, and anti-TNF-alpha antibody therapy significantly enhanced clinical and pathological outcomes. Here we describe the use of PPS for the treatment of MPS type VI rats. METHODOLOGY/PRINCIPAL FINDINGS: Treatment began during prenatal development and at 1 and 6 months of age. All animals were treated until they were 9 months old. Significant reductions in the serum and tissue levels of several inflammatory markers (e.g., TNF-alpha, MIP-1alpha and RANTES/CCL5) were observed, as was reduced expression of inflammatory markers in cultured articular chondrocytes. ADAMTS-5/aggrecanase-2 levels also were reduced in chondrocytes, consistent with an elevation of serum tissue inhibitor of metalloproteinase 1. Marked improvements in motility and grooming behavior occurred, along with a reduction in eye and nasal secretions and a lessening of the tracheal deformities. MicroCT and radiographic analyses further revealed that the treated MPS skulls were longer and thinner, and that the teeth malocclusions, misalignments and mineral densities were improved. MicroCT analysis of the femurs and vertebrae revealed improvements in trabecular bone mineral densities, number and spacing in a subset of treated MPS animals. Biomechanical assessments of PPS-treated spines showed partially restored torsional behaviors, suggesting increased spinal stability. No improvements were observed in cortical bone or femur length. The positive changes in the PPS-treated MPS VI rats occurred despite glycosaminoglycan accumulation in their tissues. CONCLUSIONS: Based on these findings we conclude that PPS could be a simple and effective therapy for MPS that might provide significant clinical benefits alone and in combination with other therapies.
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spelling pubmed-35547612013-01-30 Pentosan Polysulfate: A Novel Therapy for the Mucopolysaccharidoses Schuchman, Edward H. Ge, Yi Lai, Alon Borisov, Yury Faillace, Meghan Eliyahu, Efrat He, Xingxuan Iatridis, James Vlassara, Helen Striker, Gary Simonaro, Calogera M. PLoS One Research Article BACKGROUND: Pentosan polysulfate (PPS) is an FDA-approved, oral medication with anti-inflammatory and pro-chondrogenic properties. We have previously shown that animal models of the mucopolysaccharidoses (MPS) exhibit significant inflammatory disease, contributing to cartilage degeneration. Enzyme replacement therapy (ERT) only partly reduced inflammation, and anti-TNF-alpha antibody therapy significantly enhanced clinical and pathological outcomes. Here we describe the use of PPS for the treatment of MPS type VI rats. METHODOLOGY/PRINCIPAL FINDINGS: Treatment began during prenatal development and at 1 and 6 months of age. All animals were treated until they were 9 months old. Significant reductions in the serum and tissue levels of several inflammatory markers (e.g., TNF-alpha, MIP-1alpha and RANTES/CCL5) were observed, as was reduced expression of inflammatory markers in cultured articular chondrocytes. ADAMTS-5/aggrecanase-2 levels also were reduced in chondrocytes, consistent with an elevation of serum tissue inhibitor of metalloproteinase 1. Marked improvements in motility and grooming behavior occurred, along with a reduction in eye and nasal secretions and a lessening of the tracheal deformities. MicroCT and radiographic analyses further revealed that the treated MPS skulls were longer and thinner, and that the teeth malocclusions, misalignments and mineral densities were improved. MicroCT analysis of the femurs and vertebrae revealed improvements in trabecular bone mineral densities, number and spacing in a subset of treated MPS animals. Biomechanical assessments of PPS-treated spines showed partially restored torsional behaviors, suggesting increased spinal stability. No improvements were observed in cortical bone or femur length. The positive changes in the PPS-treated MPS VI rats occurred despite glycosaminoglycan accumulation in their tissues. CONCLUSIONS: Based on these findings we conclude that PPS could be a simple and effective therapy for MPS that might provide significant clinical benefits alone and in combination with other therapies. Public Library of Science 2013-01-24 /pmc/articles/PMC3554761/ /pubmed/23365668 http://dx.doi.org/10.1371/journal.pone.0054459 Text en © 2013 Schuchman et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Schuchman, Edward H.
Ge, Yi
Lai, Alon
Borisov, Yury
Faillace, Meghan
Eliyahu, Efrat
He, Xingxuan
Iatridis, James
Vlassara, Helen
Striker, Gary
Simonaro, Calogera M.
Pentosan Polysulfate: A Novel Therapy for the Mucopolysaccharidoses
title Pentosan Polysulfate: A Novel Therapy for the Mucopolysaccharidoses
title_full Pentosan Polysulfate: A Novel Therapy for the Mucopolysaccharidoses
title_fullStr Pentosan Polysulfate: A Novel Therapy for the Mucopolysaccharidoses
title_full_unstemmed Pentosan Polysulfate: A Novel Therapy for the Mucopolysaccharidoses
title_short Pentosan Polysulfate: A Novel Therapy for the Mucopolysaccharidoses
title_sort pentosan polysulfate: a novel therapy for the mucopolysaccharidoses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554761/
https://www.ncbi.nlm.nih.gov/pubmed/23365668
http://dx.doi.org/10.1371/journal.pone.0054459
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