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A retrievable implant for the long-term encapsulation and survival of therapeutic xenogeneic cells

The long-term function of transplanted therapeutic cells typically requires systemic immune suppression. Here, we show that a retrievable implant comprising of a silicone reservoir and a porous polymeric membrane protects human cells encapsulated in it after implant transplantation in the intraperit...

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Autores principales: Bose, Suman, Volpatti, Lisa R., Thiono, Devina, Yesilyurt, Volkan, McGladian, Collin, Tang, Yaoyu, Facklam, Amanda, Wang, Amy, Jhunjhunwala, Siddharth, Veiseh, Omid, Hollister-Lock, Jennifer, Bhattacharya, Chandrabali, Weir, Gordon C., Greiner, Dale L., Langer, Robert, Anderson, Daniel G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051527/
https://www.ncbi.nlm.nih.gov/pubmed/32231313
http://dx.doi.org/10.1038/s41551-020-0538-5
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author Bose, Suman
Volpatti, Lisa R.
Thiono, Devina
Yesilyurt, Volkan
McGladian, Collin
Tang, Yaoyu
Facklam, Amanda
Wang, Amy
Jhunjhunwala, Siddharth
Veiseh, Omid
Hollister-Lock, Jennifer
Bhattacharya, Chandrabali
Weir, Gordon C.
Greiner, Dale L.
Langer, Robert
Anderson, Daniel G.
author_facet Bose, Suman
Volpatti, Lisa R.
Thiono, Devina
Yesilyurt, Volkan
McGladian, Collin
Tang, Yaoyu
Facklam, Amanda
Wang, Amy
Jhunjhunwala, Siddharth
Veiseh, Omid
Hollister-Lock, Jennifer
Bhattacharya, Chandrabali
Weir, Gordon C.
Greiner, Dale L.
Langer, Robert
Anderson, Daniel G.
author_sort Bose, Suman
collection PubMed
description The long-term function of transplanted therapeutic cells typically requires systemic immune suppression. Here, we show that a retrievable implant comprising of a silicone reservoir and a porous polymeric membrane protects human cells encapsulated in it after implant transplantation in the intraperitoneal space of immunocompetent mice. Membranes with pores 1 µm in diameter allowed host macrophages to migrate into the device without the loss of transplanted cells, whereas membranes with pore sizes under 0.8 µm prevented their infiltration by immune cells. A synthetic polymer coating prevented fibrosis and was necessary for the long-term function of the device. For over 130 days the device supported human cells engineered to secrete erythropoietin in immunocompetent mice as well as transgenic human cells carrying an inducible gene circuit for the on-demand secretion of erythropoietin. Pancreatic islets from rats encapsulated in the device and implanted in diabetic mice restored normoglycaemia in the mice for over 75 days. The biocompatible device provides a retrievable solution for the transplantation of engineered cells in the absence of immunosuppression.
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spelling pubmed-80515272021-04-16 A retrievable implant for the long-term encapsulation and survival of therapeutic xenogeneic cells Bose, Suman Volpatti, Lisa R. Thiono, Devina Yesilyurt, Volkan McGladian, Collin Tang, Yaoyu Facklam, Amanda Wang, Amy Jhunjhunwala, Siddharth Veiseh, Omid Hollister-Lock, Jennifer Bhattacharya, Chandrabali Weir, Gordon C. Greiner, Dale L. Langer, Robert Anderson, Daniel G. Nat Biomed Eng Article The long-term function of transplanted therapeutic cells typically requires systemic immune suppression. Here, we show that a retrievable implant comprising of a silicone reservoir and a porous polymeric membrane protects human cells encapsulated in it after implant transplantation in the intraperitoneal space of immunocompetent mice. Membranes with pores 1 µm in diameter allowed host macrophages to migrate into the device without the loss of transplanted cells, whereas membranes with pore sizes under 0.8 µm prevented their infiltration by immune cells. A synthetic polymer coating prevented fibrosis and was necessary for the long-term function of the device. For over 130 days the device supported human cells engineered to secrete erythropoietin in immunocompetent mice as well as transgenic human cells carrying an inducible gene circuit for the on-demand secretion of erythropoietin. Pancreatic islets from rats encapsulated in the device and implanted in diabetic mice restored normoglycaemia in the mice for over 75 days. The biocompatible device provides a retrievable solution for the transplantation of engineered cells in the absence of immunosuppression. 2020-03-30 2020-08 /pmc/articles/PMC8051527/ /pubmed/32231313 http://dx.doi.org/10.1038/s41551-020-0538-5 Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms http://www.nature.com/reprintsReprints and permissions information is available at www.nature.com/reprints (http://www.nature.com/reprints) .
spellingShingle Article
Bose, Suman
Volpatti, Lisa R.
Thiono, Devina
Yesilyurt, Volkan
McGladian, Collin
Tang, Yaoyu
Facklam, Amanda
Wang, Amy
Jhunjhunwala, Siddharth
Veiseh, Omid
Hollister-Lock, Jennifer
Bhattacharya, Chandrabali
Weir, Gordon C.
Greiner, Dale L.
Langer, Robert
Anderson, Daniel G.
A retrievable implant for the long-term encapsulation and survival of therapeutic xenogeneic cells
title A retrievable implant for the long-term encapsulation and survival of therapeutic xenogeneic cells
title_full A retrievable implant for the long-term encapsulation and survival of therapeutic xenogeneic cells
title_fullStr A retrievable implant for the long-term encapsulation and survival of therapeutic xenogeneic cells
title_full_unstemmed A retrievable implant for the long-term encapsulation and survival of therapeutic xenogeneic cells
title_short A retrievable implant for the long-term encapsulation and survival of therapeutic xenogeneic cells
title_sort retrievable implant for the long-term encapsulation and survival of therapeutic xenogeneic cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051527/
https://www.ncbi.nlm.nih.gov/pubmed/32231313
http://dx.doi.org/10.1038/s41551-020-0538-5
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