Editorial: First Regulatory Approval for Allogeneic Pancreatic Islet Beta Cell Infusion for Adult Patients with Type 1 Diabetes Mellitus.

Dinah V Parums
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Abstract

Type 1 diabetes mellitus affects adults and children, with an increasing number of newly-diagnosed cases each year. Type 1 diabetes involves a primary functional defect in pancreatic islet beta cells, resulting in secondary autoimmunity that results in T-cell-mediated beta cell death. However, pancreatic transplantation is a complex procedure, with complications that include transplant organ failure due to rejection or ischemia-reperfusion injury, safety issues of the duodenal-duodenal anastomosis technique, and the availability of segmental or whole organs. On June 28, 2023, the FDA Center for Biologics Evaluation and Research (CBER) approved Lantidra (donislecel), the first allogeneic (deceased donor) pancreatic islet cell therapy for the treatment of adults with type 1 diabetes who do not achieve target glycated hemoglobin levels because of repeated episodes of severe hypoglycemia, despite current management. This Editorial aims to highlight the increasing global health burden of type 1 diabetes, previous approaches to pancreatic transplant methods and introduces the first regulatory approval for allogeneic pancreatic islet beta cell infusion, a novel approach to transplantation.

编辑:首次批准异体胰岛β细胞输注治疗成人1型糖尿病患者。
1型糖尿病影响成人和儿童,每年新诊断的病例数量不断增加。1型糖尿病涉及胰岛β细胞的原发性功能缺陷,导致继发性自身免疫,导致t细胞介导的β细胞死亡。然而,胰腺移植是一个复杂的过程,其并发症包括由于排斥反应或缺血再灌注损伤引起的移植器官衰竭,十二指肠-十二指肠吻合技术的安全性问题,以及节段性或整个器官的可用性。2023年6月28日,FDA生物制品评估和研究中心(CBER)批准了Lantidra (donislecel),这是第一个同种异体(已故供体)胰岛细胞疗法,用于治疗由于反复发作的严重低血糖而无法达到目标糖化血红蛋白水平的成人1型糖尿病患者,尽管目前的治疗方法。这篇社论旨在强调1型糖尿病日益增加的全球健康负担,先前的胰腺移植方法,并介绍了第一个监管机构批准的异体胰岛β细胞输注,这是一种新的移植方法。
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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