Potential for clinical pancreatic islet xenotransplantation

IF 0.1 Q4 TRANSPLANTATION
R. Bottino, S. Nagaraju, V. Satyananda, H. Hara, M. Wijkstrom, M. Trucco, D. Cooper
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引用次数: 1

Abstract

© 2014 Bottino et al. Diabetes mellitus is increasing worldwide. Type 1 diabetes can be treated successfully by islet allotransplantation, the results of which are steadily improving. However, the number of islets that can be obtained from deceased human donors will never be sufficient to cure more than a very small percentage of patients who might benefit from transplantation. Although there are some differences in glucose metabolism between pigs and humans, the use of pigs could provide an unlimited supply of islets, and the insulin produced would undoubtedly control glucose levels. Transplantation of islets into the portal vein results in islets residing in the liver; however, an early inflammatory response and rejection remain problematic, even when the recipient is receiving immunosuppressive therapy. In the long term, immunosuppressive drugs may exhibit toxicities to patients and specifically harm the islet cells. In contrast, encapsulation techniques provide islets with a physical barrier that prevents antibodies binding to the islet graft while still allowing insulin to be released into the recipient’s circulation; in theory, patients receiving encapsulated grafts might not require exogenous immunosuppressive therapy. Nonhuman primates with encapsulated pig islet transplants have remained insulin-independent for several weeks, but long-term efficacy remains uncertain. Furthermore, techniques are now available to knock out genes from the pig and/or insert human genes, thus rendering the antigenic structure of pigs closer to that of humans, and providing protection from the human immune response. Islet transplantation from genetically engineered pigs has been followed by insulin independence in a small number of nonhuman primates for greater than 1 year. Neonatal islets have some advantages over adult islets in that they are easier to isolate and culture, and have the ability to proliferate during the first few months after transplantation. In 2009, the International Xenotransplantation Association set up a group to encourage and advise on clinical trials of pig islet xenotransplantation; this group’s guidelines are discussed. Clinical trials of encapsulated pig islets are already under way.
临床胰岛异种移植的潜力
©2014 Bottino et al。糖尿病在世界范围内呈上升趋势。同种异体胰岛移植可以成功治疗1型糖尿病,其结果正在稳步改善。然而,从死亡的人类供体中获得的胰岛数量永远不足以治愈可能从移植中受益的一小部分患者。尽管猪和人在葡萄糖代谢方面存在一些差异,但使用猪可以提供无限的胰岛供应,并且产生的胰岛素无疑会控制血糖水平。将胰岛移植到门静脉导致胰岛驻留在肝脏中;然而,早期的炎症反应和排斥反应仍然存在问题,即使受体接受免疫抑制治疗。从长期来看,免疫抑制药物可能对患者产生毒性,并特异性地损害胰岛细胞。相比之下,封装技术为胰岛提供了一个物理屏障,防止抗体与胰岛移植物结合,同时仍允许胰岛素释放到受体的循环中;理论上,接受包封移植物的患者可能不需要外源性免疫抑制治疗。非人类灵长类动物接受封装的猪胰岛移植后,仍可保持胰岛素独立数周,但长期疗效仍不确定。此外,现在有技术可以从猪中敲除基因和/或插入人类基因,从而使猪的抗原结构更接近人类,并提供对人类免疫反应的保护。经过基因工程改造的猪的胰岛移植后,少数非人灵长类动物的胰岛素依赖性已超过1年。新生儿胰岛比成人胰岛有一些优势,因为它们更容易分离和培养,并且在移植后的最初几个月内具有增殖能力。2009年,国际异种移植协会成立了一个小组,鼓励和建议猪胰岛异种移植的临床试验;讨论了该小组的指导方针。猪胰岛封装的临床试验已经在进行中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
6
审稿时长
16 weeks
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