z-logo
open-access-imgOpen Access
Nanoporous Immunoprotective Device for Stem-Cell-Derived β-Cell Replacement Therapy
Author(s) -
R. Shihman Chang,
Gaetano Faleo,
Holger A. Russ,
Audrey V. Parent,
Susanna K. Elledge,
Daniel A. Bernards,
Jessica L. Allen,
Karina E. Villanueva,
Matthias Hebrok,
Qizhi Tang,
Tejal A. Desai
Publication year - 2017
Publication title -
acs nano
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/acsnano.7b01239
Subject(s) - immune system , cell encapsulation , stem cell , embryonic stem cell , in vivo , viability assay , biocompatibility , cell therapy , stem cell therapy , cell , microbiology and biotechnology , materials science , biology , nanotechnology , immunology , biochemistry , gene , metallurgy
Encapsulation of human embryonic stem-cell-differentiated beta cell clusters (hES-βC) holds great promise for cell replacement therapy for the treatment of diabetics without the need for chronic systemic immune suppression. Here, we demonstrate a nanoporous immunoprotective polymer thin film cell encapsulation device that can exclude immune molecules while allowing exchange of oxygen and nutrients necessary for in vitro and in vivo stem cell viability and function. Biocompatibility studies show the device promotes neovascular formation with limited foreign body response in vivo. The device also successfully prevented teratoma escape into the peritoneal cavity of mice. Long-term animal studies demonstrate evidence of engraftment, viability, and function of cells encapsulated in the device after 6 months. Finally, in vivo study confirms that the device was able to effectively immuno-isolate cells from the host immune system.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom