Grattoni Alessandro, Korbutt Gregory, Tomei Alice A, García Andrés J, Pepper Andrew R, Stabler Cherie, Brehm Michael, Papas Klearchos, Citro Antonio, Shirwan Haval, Millman Jeffrey R, Melero-Martin Juan, Graham Melanie, Sefton Michael, Ma Minglin, Kenyon Norma, Veiseh Omid, Desai Tejal A, Nostro M Cristina, Marinac Marjana, Sykes Megan, Russ Holger A, Odorico Jon, Tang Qizhi, Ricordi Camillo, Latres Esther, Mamrak Nicholas E, Giraldo Jaime, Poznansky Mark C, de Vos Paul
Department of Nanomedicine, Houston Methodist Research Institute, Houston, TX, USA.
Department of Surgery, Houston Methodist Hospital, Houston, TX, USA.
Nat Rev Endocrinol. 2025 Jan;21(1):14-30. doi: 10.1038/s41574-024-01029-0. Epub 2024 Sep 3.
Type 1 diabetes mellitus (T1DM) is a growing global health concern that affects approximately 8.5 million individuals worldwide. T1DM is characterized by an autoimmune destruction of pancreatic β cells, leading to a disruption in glucose homeostasis. Therapeutic intervention for T1DM requires a complex regimen of glycaemic monitoring and the administration of exogenous insulin to regulate blood glucose levels. Advances in continuous glucose monitoring and algorithm-driven insulin delivery devices have improved the quality of life of patients. Despite this, mimicking islet function and complex physiological feedback remains challenging. Pancreatic islet transplantation represents a potential functional cure for T1DM but is hindered by donor scarcity, variability in harvested cells, aggressive immunosuppressive regimens and suboptimal clinical outcomes. Current research is directed towards generating alternative cell sources, improving transplantation methods, and enhancing cell survival without chronic immunosuppression. This Review maps the progress in cell replacement therapies for T1DM and outlines the remaining challenges and future directions. We explore the state-of-the-art strategies for generating replenishable β cells, cell delivery technologies and local targeted immune modulation. Finally, we highlight relevant animal models and the regulatory aspects for advancing these technologies towards clinical deployment.
1型糖尿病(T1DM)是一个日益受到全球关注的健康问题,全球约有850万人受其影响。T1DM的特征是胰腺β细胞发生自身免疫性破坏,导致葡萄糖稳态紊乱。T1DM的治疗干预需要复杂的血糖监测方案以及给予外源性胰岛素来调节血糖水平。连续血糖监测和算法驱动的胰岛素输送装置的进展改善了患者的生活质量。尽管如此,模拟胰岛功能和复杂的生理反馈仍然具有挑战性。胰岛移植是T1DM潜在的功能性治愈方法,但受到供体稀缺、收获细胞的变异性、激进的免疫抑制方案以及不理想的临床结果的阻碍。当前的研究方向是生成替代细胞来源、改进移植方法以及在无慢性免疫抑制的情况下提高细胞存活率。本综述梳理了T1DM细胞替代疗法的进展,并概述了 remaining challenges(此处原文有误,可能是remaining challenges,翻译为“剩余挑战”)和未来方向。我们探讨了生成可补充β细胞的前沿策略、细胞递送技术和局部靶向免疫调节。最后,我们强调了相关动物模型以及将这些技术推进到临床应用的监管方面。