Advances in islet encapsulation technologies (vol 16, pg 338, 2017)

被引:1
作者
Desai, Tejal
Shea, Lonnie D.
机构
[1] University of California, San Francisco, Department of Bioengineering and Therapeutic Sciences, 1700 4th Street, San Francisco, 94158-2330, CA
[2] University of Michigan, Department of Biomedical Engineering, 2200 Bonisteel Boulevard, Ann Arbor, 48109-2099, MI
关键词
D O I
10.1038/nrd.2017.67
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Type 1 diabetes is an autoimmune disorder in which the immune system attacks and destroys insulin-producing islet cells of the pancreas. Although islet transplantation has proved to be successful for some patients with type 1 diabetes, its widespread use is limited by islet donor shortage and the requirement for lifelong immunosuppression. An encapsulation strategy that can prevent the rejection of xenogeneic islets or of stem cell-derived allogeneic islets can potentially eliminate both of these barriers. Although encapsulation technology has met several challenges, the convergence of expertise in materials, nanotechnology, stem cell biology and immunology is allowing us to get closer to the goal of encapsulated islet cell therapy for humans.
引用
收藏
页码:338 / 350
页数:1
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[1]  
Desai T, 2017, NAT REV DRUG DISCOV, V16, P338, DOI 10.1038/nrd.2016.232