Islet encapsulation

被引:39
作者
Ernst, Alexander Ulrich [1 ]
Wang, Long-Hai [1 ]
Ma, Minglin [1 ]
机构
[1] Cornell Univ, Dept Biol & Environm Engn, Ithaca, NY 14853 USA
关键词
REGULATORY T-CELLS; POLY(ETHYLENE GLYCOL) DIACRYLATE; TYPE-1; DIABETIC-PATIENT; BETA-CELLS; PANCREATIC-ISLETS; IN-VITRO; NONIMMUNOSUPPRESSED PATIENTS; MICROENCAPSULATED ISLETS; COMPOSITE MICROCAPSULES; MACROPHAGE POLARIZATION;
D O I
10.1039/c8tb02020e
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
This review focuses on recent engineering advances in islet encapsulation technologies. beta-cell replacement therapy in the form of allogeneic naked islet transplantation has become an established treatment for type 1 diabetes mellitus (T1DM). However, some limitations still impact the broad applicability and long-term efficacy of the procedure, including shortage of donor islets, the need for lifelong immunosuppression, and restriction to the most vulnerable patients. Islet encapsulation promises to overcome these constraints by providing a selectively permeable barrier between host and therapeutic tissues. While tremendous progress has been made and the clearing of key translational hurdles appears to be near, many challenges need to be addressed before this technology platform can enter the clinic. Here, we summarize the research in this area and seek to identify the outstanding challenges in translating islet encapsulation technology to human patients.
引用
收藏
页码:6705 / 6722
页数:18
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