Augmenting engraftment of beta cell replacement therapies for T1DM

Saloni Aggarwal , Andrew R. Pepper , Najwa Al Jahdhami
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引用次数: 1

Abstract

Objectives

For nearly a century, the therapeutic use of exogenous insulin remains the gold standard treatment strategy for patients living with Type 1 Diabetes Mellitus (T1DM). While lifesaving, insulin can fail to prevent the secondary vascular disease and complications inherited with T1DM diagnosis, and for some, this may increase their risk of life-threatening hypoglycemic unawareness. In recent decades transplantation has been demonstrated as the only means (a replacement gold standard therapy) to effectively restore physiologically relevant glycemic control. Moreover, significant advancements in clinical islet transplantation have yielded greater incidences of durable insulin-independence, rescindment of critical hypoglycemia and prevention of comorbidities. Yet, the requisite of life-long immunosuppression and scarcity of a universal and potent cell supply, in addition to the challenges faced with such therapy in vivo, restricts the broad-spectrum application of cell-based therapies.

Key findings

Herein, this review presents the history, current status and persisting challenges confronting cell-based replacement therapies for T1DM. Lastly, we examine modern and future research opportunities designed to enhance the efficacy of cellular transplantation, thereby offering a potential functional cure to all those affected by T1DM.

Conclusions

Given the rapid progress in β-cell replacement therapy, it is hopeful that through multidisciplinary innovations, first-in-human stem cell trials, innocuous immunosuppression and efficacious extrahepatic transplant sites, β-cell replacement therapies will become the cornerstone treatment for the millions worldwide afflicated with T1DM.

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增强植入β细胞替代疗法治疗T1DM
近一个世纪以来,外源性胰岛素治疗一直是1型糖尿病(T1DM)患者的金标准治疗策略。虽然可以挽救生命,但胰岛素不能预防继发性血管疾病和T1DM遗传并发症,对一些人来说,这可能会增加他们危及生命的低血糖无意识的风险。近几十年来,移植已被证明是有效恢复生理相关血糖控制的唯一手段(替代金标准疗法)。此外,临床胰岛移植的重大进展已经产生了更大的持久胰岛素独立性发生率,严重低血糖的消除和合并症的预防。然而,终身免疫抑制的必要性和普遍有效的细胞供应的稀缺性,以及这种治疗在体内面临的挑战,限制了细胞治疗的广谱应用。本文综述了基于细胞的T1DM替代疗法的历史、现状和面临的持续挑战。最后,我们研究了旨在提高细胞移植疗效的现代和未来的研究机会,从而为所有受T1DM影响的患者提供潜在的功能性治疗。鉴于β细胞替代疗法的快速发展,通过多学科创新、首次人体干细胞试验、无害免疫抑制和有效的肝外移植,β细胞替代疗法有望成为全球数百万T1DM患者的基石治疗方法。
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