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用于糖尿病治疗的胰岛细胞封装:历史、当前进展和需要解决的关键问题。

Encapsulated islets for diabetes therapy: history, current progress, and critical issues requiring solution.

机构信息

Prodo Laboratories & Scharp-Lacy Research Institute, 32A Mauchly, Irvine, CA 92618, USA.

Department of Endocrinology and Metabolism, Metabolic Unit, Cisanello Hospital, University of Pisa, Via Paradise 2, Pisa 56100, Italy.

出版信息

Adv Drug Deliv Rev. 2014 Apr;67-68:35-73. doi: 10.1016/j.addr.2013.07.018. Epub 2013 Aug 1.

Abstract

Insulin therapy became a reality in 1921 dramatically saving lives of people with diabetes, but not protecting them from long-term complications. Clinically successful free islet implants began in 1989 but require life long immunosuppression. Several encapsulated islet approaches have been ongoing for over 30 years without defining a clinically relevant product. Macro-devices encapsulating islet mass in a single device have shown long-term success in large animals but human trials have been limited by critical challenges. Micro-capsules using alginate or similar hydrogels encapsulate individual islets with many hundreds of promising rodent results published, but a low incidence of successful translation to large animal and human results. Reduction of encapsulated islet mass for clinical transplantation is in progress. This review covers the status of both early and current studies including the presentation of corporate efforts involved. It concludes by defining the critical items requiring solution to enable a successful clinical diabetes therapy.

摘要

胰岛素治疗于 1921 年成为现实,极大地挽救了糖尿病患者的生命,但并不能防止他们患上长期并发症。1989 年开始临床成功的游离胰岛移植,但需要终身免疫抑制。多年来,已经有几种封装胰岛的方法在进行,但尚未确定一种具有临床相关性的产品。在大型动物中,封装胰岛的大型设备已显示出长期成功,但人体试验受到关键挑战的限制。使用藻酸盐或类似水凝胶的微胶囊可封装数百个有前途的啮齿动物胰岛,已有大量相关研究发表,但成功转化为大型动物和人类结果的比例较低。目前正在进行减少临床移植用封装胰岛质量的研究。本综述涵盖了早期和当前研究的现状,包括所涉及的公司努力的介绍。最后,它定义了需要解决的关键问题,以实现成功的临床糖尿病治疗。

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