Desai Tejal, Shea Lonnie D
University of California, San Francisco, Department of Bioengineering and Therapeutic Sciences, Byers Hall Rm 203C, MC 2520, 1700 4th Street, San Francisco, California 94158-2330, USA.
University of Michigan, Department of Biomedical Engineering, 1119 Carl A. Gerstacker Building, 2200 Bonisteel Boulevard, Ann Arbor, Michigan 48109-2099, USA.
Nat Rev Drug Discov. 2017 May;16(5):338-350. doi: 10.1038/nrd.2016.232. Epub 2016 Dec 23.
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.
1型糖尿病是一种自身免疫性疾病,免疫系统会攻击并破坏胰腺中产生胰岛素的胰岛细胞。尽管胰岛移植已被证明对一些1型糖尿病患者是成功的,但其广泛应用受到胰岛供体短缺和终身免疫抑制需求的限制。一种能够防止异种胰岛或干细胞衍生的同种异体胰岛被排斥的封装策略有可能消除这两个障碍。尽管封装技术面临一些挑战,但材料、纳米技术、干细胞生物学和免疫学等领域专业知识的融合使我们更接近人类胰岛细胞封装治疗的目标。