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用于评估基于干细胞的胰岛细胞移植的人源化小鼠模型的现状、障碍和未来方向。

Current Status, Barriers, and Future Directions for Humanized Mouse Models to Evaluate Stem Cell-Based Islet Cell Transplant.

机构信息

Department of Surgery, University of Alberta, Edmonton, AB, Canada.

National Institute of Medical Sciences and Nutrition Salvador Zubiran, Mexico City, Mexico.

出版信息

Adv Exp Med Biol. 2022;1387:89-106. doi: 10.1007/5584_2022_711.

Abstract

Islet cell transplant (ITx) continues to improve, with recently published long-term outcomes suggesting nearly 80% graft survival, leading to improvements in glycemic control, reductions in insulin doses, and near-complete abrogation of severe hypoglycemia. Unfortunately, access to ITx remains limited by immunosuppression requirements and donor supply. Discovery of stem cell-derived functional islet-like clusters with the capacity to reverse diabetes offers a renewable, potentially immunosuppression-free solution for future widespread ITx. Evaluation and optimization of these therapies is ongoing, but may one day provide a realistic cure for type 1 diabetes. However, stem cell-based ITx has unique immunologic questions that remain unanswered. Here, we briefly synthesize current approaches for stem cell-derived ITx, review humanized mice models, and elaborate on the potential of humanized mice models for bridging the gap between current small rodent models and human clinical trials for allogeneic and autologous inducible pluripotent stem cell (iPSC)-based ITx while highlighting limitations and future directions.

摘要

胰岛细胞移植(ITx)不断完善,最近发表的长期结果表明,近 80%的移植物存活,导致血糖控制改善、胰岛素剂量减少,以及严重低血糖的几乎完全消除。然而,由于免疫抑制的需求和供体供应的限制,ITx 的应用仍然有限。发现具有逆转糖尿病能力的干细胞衍生的功能性胰岛样簇为未来广泛的 ITx 提供了一种可再生的、潜在无免疫抑制的解决方案。这些疗法的评估和优化正在进行中,但可能有一天会为 1 型糖尿病提供一种现实的治疗方法。然而,基于干细胞的 ITx 存在一些尚未解决的独特免疫学问题。在这里,我们简要总结了目前用于干细胞衍生 ITx 的方法,回顾了人源化小鼠模型,并详细阐述了人源化小鼠模型在连接当前小啮齿动物模型与人同种异体和自体诱导多能干细胞(iPSC)基于 ITx 的临床试验方面的潜力,同时强调了其局限性和未来方向。

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