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Engineering autonomous closed-loop designer cells for disease therapy

Synthetic biology has made it possible to engineer mammalian cells for on-demand delivery of therapeutic agents, providing therapeutic solutions for chronic or intractable diseases. Currently, most of the engineered therapeutic cells are regulated by the administration of exogenous inducers, but the...

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Detalles Bibliográficos
Autores principales: Mahameed, Mohamed, Fussenegger, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857602/
https://www.ncbi.nlm.nih.gov/pubmed/35243222
http://dx.doi.org/10.1016/j.isci.2022.103834
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author Mahameed, Mohamed
Fussenegger, Martin
author_facet Mahameed, Mohamed
Fussenegger, Martin
author_sort Mahameed, Mohamed
collection PubMed
description Synthetic biology has made it possible to engineer mammalian cells for on-demand delivery of therapeutic agents, providing therapeutic solutions for chronic or intractable diseases. Currently, most of the engineered therapeutic cells are regulated by the administration of exogenous inducers, but the need for repeated administration of these xenobiotics is problematic from the viewpoints of patients' compliance and quality of life, as well as possible side effects. Recently, synthetic biologists started to address these issues by constructing autonomous, closed-loop therapeutic cells, often referred to as designer cells. These cells are equipped with sensing modules that detect and link marker(s) of the target disease to signaling cascades that stimulate the secretion of specified therapeutic agents in a timely and quantitative manner, without the need of exogenous inducers. Here, we review recent work on designer cell engineering and their in vivo therapeutic applications, focusing on the molecular mechanisms and signaling pathways employed.
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spelling pubmed-88576022022-03-02 Engineering autonomous closed-loop designer cells for disease therapy Mahameed, Mohamed Fussenegger, Martin iScience Review Synthetic biology has made it possible to engineer mammalian cells for on-demand delivery of therapeutic agents, providing therapeutic solutions for chronic or intractable diseases. Currently, most of the engineered therapeutic cells are regulated by the administration of exogenous inducers, but the need for repeated administration of these xenobiotics is problematic from the viewpoints of patients' compliance and quality of life, as well as possible side effects. Recently, synthetic biologists started to address these issues by constructing autonomous, closed-loop therapeutic cells, often referred to as designer cells. These cells are equipped with sensing modules that detect and link marker(s) of the target disease to signaling cascades that stimulate the secretion of specified therapeutic agents in a timely and quantitative manner, without the need of exogenous inducers. Here, we review recent work on designer cell engineering and their in vivo therapeutic applications, focusing on the molecular mechanisms and signaling pathways employed. Elsevier 2022-01-29 /pmc/articles/PMC8857602/ /pubmed/35243222 http://dx.doi.org/10.1016/j.isci.2022.103834 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Mahameed, Mohamed
Fussenegger, Martin
Engineering autonomous closed-loop designer cells for disease therapy
title Engineering autonomous closed-loop designer cells for disease therapy
title_full Engineering autonomous closed-loop designer cells for disease therapy
title_fullStr Engineering autonomous closed-loop designer cells for disease therapy
title_full_unstemmed Engineering autonomous closed-loop designer cells for disease therapy
title_short Engineering autonomous closed-loop designer cells for disease therapy
title_sort engineering autonomous closed-loop designer cells for disease therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857602/
https://www.ncbi.nlm.nih.gov/pubmed/35243222
http://dx.doi.org/10.1016/j.isci.2022.103834
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