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Modifying enzyme replacement therapy – A perspective

Several diseases are caused by the lack of functional proteins, including lysosomal storage diseases or haemophilia A and B. Patients suffering from one of these diseases are treated via enzyme replacement therapies to restore the missing protein. Although this treatment strategy prevents some disea...

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Detalles Bibliográficos
Autor principal: Schaible, Philipp
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843529/
https://www.ncbi.nlm.nih.gov/pubmed/36566487
http://dx.doi.org/10.1111/jcmm.17653
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author Schaible, Philipp
author_facet Schaible, Philipp
author_sort Schaible, Philipp
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description Several diseases are caused by the lack of functional proteins, including lysosomal storage diseases or haemophilia A and B. Patients suffering from one of these diseases are treated via enzyme replacement therapies to restore the missing protein. Although this treatment strategy prevents some disease symptoms, enzyme replacement therapies are very expensive and require very frequent infusions, which can cause infusion adverse reactions and massively impair the quality of life of the patients. This review proposes a technology to sustainably produce proteins within the patient to potentially make frequent protein‐infusions redundant. This technology is based on blood circulating immune cells as producers of the needed therapeutic protein. To ensure a stable protein concentration over time the cells are equipped with a system, which induces cell proliferation when low therapeutic protein levels are detected and a system inhibiting cell proliferation when high therapeutic protein levels are detected.
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spelling pubmed-98435292023-01-23 Modifying enzyme replacement therapy – A perspective Schaible, Philipp J Cell Mol Med Review Several diseases are caused by the lack of functional proteins, including lysosomal storage diseases or haemophilia A and B. Patients suffering from one of these diseases are treated via enzyme replacement therapies to restore the missing protein. Although this treatment strategy prevents some disease symptoms, enzyme replacement therapies are very expensive and require very frequent infusions, which can cause infusion adverse reactions and massively impair the quality of life of the patients. This review proposes a technology to sustainably produce proteins within the patient to potentially make frequent protein‐infusions redundant. This technology is based on blood circulating immune cells as producers of the needed therapeutic protein. To ensure a stable protein concentration over time the cells are equipped with a system, which induces cell proliferation when low therapeutic protein levels are detected and a system inhibiting cell proliferation when high therapeutic protein levels are detected. John Wiley and Sons Inc. 2022-12-25 /pmc/articles/PMC9843529/ /pubmed/36566487 http://dx.doi.org/10.1111/jcmm.17653 Text en © 2022 The Author. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Schaible, Philipp
Modifying enzyme replacement therapy – A perspective
title Modifying enzyme replacement therapy – A perspective
title_full Modifying enzyme replacement therapy – A perspective
title_fullStr Modifying enzyme replacement therapy – A perspective
title_full_unstemmed Modifying enzyme replacement therapy – A perspective
title_short Modifying enzyme replacement therapy – A perspective
title_sort modifying enzyme replacement therapy – a perspective
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843529/
https://www.ncbi.nlm.nih.gov/pubmed/36566487
http://dx.doi.org/10.1111/jcmm.17653
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