Department of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Department of Biomaterials, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Tissue Eng Part B Rev. 2022 Feb;28(1):129-140. doi: 10.1089/ten.TEB.2020.0326. Epub 2021 Feb 24.
Islet transplantation is a promising therapy for insulin-dependent diabetes, but large-scale application is hampered by the lack of a consistent source of insulin-producing cells and need for lifelong administration of immunosuppressive drugs, which are associated with severe side effects. To avoid chronic immunosuppression, islet grafts can be enveloped in immunoisolating polymeric membranes. These immunoisolating polymeric membranes protect islet grafts from cell-mediated rejection while allowing diffusion of oxygen, nutrients, and insulin. Although clinical trials have shown the safety and feasibility of encapsulated islets to control glucose homeostasis, the strategy does up till now not support long-term graft survival. This partly can be explained by a significant loss of insulin-producing cells in the immediate period after implantation. The loss can be prevented by combining immunoisolation with immunomodulation, such as combined administration of immunomodulating cytokines or coencapsulation of immunomodulating cell types such as regulatory T cells, mesenchymal stem cells, or Sertoli cells. Also, administration of specific antibodies or apoptotic donor leucocytes is considered to create a tolerant microenvironment around immunoisolated grafts. In this review, we describe the outcomes and limitations of these approaches, as well as the recent progress in immunoisolating devices. Impact statement Immunoisolation by enveloping islets in semipermeable membranes allows for successful transplantation of islet grafts in the absence of chronic immunosuppression, but the duration of graft survival is still not permanent. The reasons for long-term final graft failure is not fully understood, but combining immunoisolation with immunomodulation of tissues or host immune system has been proposed to enhance the longevity of grafts. This article reviews the recent progress and challenges of immunoisolation, as well as the benefits and feasibility of combining encapsulation approaches with immunomodulation to promote longevity of encapsulated grafts.
胰岛移植是治疗胰岛素依赖型糖尿病的一种很有前途的方法,但由于缺乏稳定的胰岛素分泌细胞来源和需要终身使用免疫抑制药物,其大规模应用受到了阻碍,而这些药物会引起严重的副作用。为了避免慢性免疫抑制,可以将胰岛移植包裹在免疫隔离的聚合物膜中。这些免疫隔离聚合物膜可以保护胰岛移植免受细胞介导的排斥反应,同时允许氧气、营养物质和胰岛素扩散。尽管临床试验已经证明了包被胰岛控制血糖稳态的安全性和可行性,但该策略迄今为止并不能支持长期的移植物存活。这在一定程度上可以解释为在植入后立即发生大量胰岛素分泌细胞丧失。通过将免疫隔离与免疫调节相结合,如联合给予免疫调节细胞因子或共包封免疫调节细胞类型,如调节性 T 细胞、间充质干细胞或 Sertoli 细胞,可以防止这种细胞丧失。此外,给予特异性抗体或凋亡供体细胞被认为可以在免疫隔离移植物周围创造一个耐受的微环境。在这篇综述中,我们描述了这些方法的结果和局限性,以及免疫隔离装置的最新进展。