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The Inflammation in the Cytopathology of Patients With Mucopolysaccharidoses- Immunomodulatory Drugs as an Approach to Therapy.
Wiesinger, Anna-Maria; Bigger, Brian; Giugliani, Roberto; Scarpa, Maurizio; Moser, Tobias; Lampe, Christina; Kampmann, Christoph; Lagler, Florian B.
Afiliación
  • Wiesinger AM; Institute of Congenital Metabolic Diseases, Paracelsus Medical University, Salzburg, Austria.
  • Bigger B; European Reference Network for Hereditary Metabolic Diseases, MetabERN, Udine, Italy.
  • Giugliani R; European Reference Network for Hereditary Metabolic Diseases, MetabERN, Udine, Italy.
  • Scarpa M; Stem Cell and Neurotherapies, Division of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
  • Moser T; Department of Genetics, Medical Genetics Service and Biodiscovery Laboratory, HCPA, UFRGS, Porto Alegre, Brazil.
  • Lampe C; European Reference Network for Hereditary Metabolic Diseases, MetabERN, Udine, Italy.
  • Kampmann C; Regional Coordinating Center for Rare Diseases, University Hospital Udine, Udine, Italy.
  • Lagler FB; Department of Neurology, Christian Doppler University Hospital, Paracelsus Medical University, Salzburg, Austria.
Front Pharmacol ; 13: 863667, 2022.
Article en En | MEDLINE | ID: mdl-35645812
ABSTRACT
Mucopolysaccharidoses (MPS) are a group of lysosomal storage diseases (LSDs), characterized by the accumulation of glycosaminoglycans (GAGs). GAG storage-induced inflammatory processes are a driver of cytopathology in MPS and pharmacological immunomodulation can bring improvements in brain, cartilage and bone pathology in rodent models. This manuscript reviews current knowledge with regard to inflammation in MPS patients and provides hypotheses for the therapeutic use of immunomodulators in MPS. Thus, we aim to set the foundation for a rational repurposing of the discussed molecules to minimize the clinical unmet needs still remaining despite enzyme replacement therapy (ERT) and hematopoietic stem cell transplantation (HSCT).
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Front Pharmacol Año: 2022 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Front Pharmacol Año: 2022 Tipo del documento: Article País de afiliación: Austria