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

被引:125
作者
Bose, Suman [1 ]
Volpatti, Lisa R. [1 ,2 ]
Thiono, Devina [1 ,3 ]
Yesilyurt, Volkan [1 ,3 ]
McGladrigan, Collin [1 ,3 ]
Tang, Yaoyu [1 ,3 ]
Facklam, Amanda [1 ]
Wang, Amy [2 ]
Jhunjhunwala, Siddharth [1 ,7 ]
Veiseh, Omid [1 ,8 ]
Hollister-Lock, Jennifer [4 ]
Bhattacharya, Chandrabali [1 ]
Weir, Gordon C. [4 ]
Greiner, Dale L. [5 ]
Langer, Robert [1 ,2 ,3 ,6 ]
Anderson, Daniel G. [1 ,2 ,3 ,6 ]
机构
[1] MIT, David H Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[3] Boston Childrens Hosp, Dept Anesthesiol, Boston, MA 02115 USA
[4] Joslin Diabet Ctr, Res Div, Sect Islet Cell & Regenerat Biol, Boston, MA 02215 USA
[5] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA USA
[6] MIT, Inst Med Engn & Sci, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[7] Indian Inst Sci, Ctr BioSyst Sci & Engn, Bengaluru, India
[8] Rice Univ, Dept Bioengn, Houston, TX USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
BETA-CELLS; ERYTHROPOIETIN; ISLETS; DEVICE; TRANSPLANTATION; MIGRATION; MEMBRANES; DELIVERY; MICE;
D O I
10.1038/s41551-020-0538-5
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A retrievable, porous and anti-fibrotic macrodevice for the encapsulation of cells provides long-term protection to human cells expressing therapeutic proteins after device implantation in the intraperitoneal space of immunocompetent mice. The long-term function of transplanted therapeutic cells typically requires systemic immune suppression. Here, we show that a retrievable implant comprising 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 mu m in diameter allowed host macrophages to migrate into the device without the loss of transplanted cells, whereas membranes with pore sizes 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.
引用
收藏
页码:814 / 826
页数:13
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