1型糖尿病治疗的未来

Anette-Gabriele Ziegler, Eda Cengiz, Thomas W H Kay
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摘要

1型糖尿病的治疗正在进入一个变革的时代。Teplizumab是首个延迟临床1型糖尿病发病的免疫疗法,已获得美国食品和药物管理局(fda)批准。其他基于免疫的疗法显示出保留β细胞功能的希望。使用胰岛自身抗体的公共健康筛查正在扩大,使早期诊断成为可能,减少糖尿病酮症酸中毒,并允许在需要胰岛素治疗之前及时引入疾病改善治疗。β细胞替代正在从传统的供体胰岛和胰腺移植转向干细胞来源的β细胞。生物工程方法(如封装和基因编辑)可以创造低免疫细胞,从而减少阻碍β细胞替代的免疫抑制需求,而患者来源的干细胞为个性化治疗打开了大门。虽然这些创新已经提供给少数患者,但将其扩展到广泛使用仍然是一个挑战。与此同时,通过使用将血糖监测与胰岛素泵相结合的自动胰岛素输送系统,葡萄糖调节正在得到改善。新一代胰岛素(那些超快速、超持久和葡萄糖反应的胰岛素)通过最小化血糖波动来改善结果。总之,这些突破为改善1型糖尿病患者的长期管理和生活质量带来了新的希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The future of type 1 diabetes therapy
The treatment of type 1 diabetes is entering a transformative era. Teplizumab, the first immunotherapy treatment to delay the onset of clinical type 1 diabetes, has been approved by the US Food and Drug Administration. Other immune-based therapies show promise in preserving β-cell function. Public health screening using islet autoantibodies is expanding, enabling earlier diagnosis, reducing diabetic ketoacidosis, and allowing timely introduction of disease-modifying treatments before the need for insulin therapy. β-cell replacement is shifting from traditional transplantation of organ donor islets and the pancreas to stem cell-derived β cells. Bioengineering methods, such as encapsulation, and gene editing to create hypoimmune cells could reduce the need for immunosuppression that has hampered β-cell replacement, and patient-derived stem cells open doors to personalised therapies. Although these innovations have been made available to a small number of patients, scaling them to widespread use remains a challenge. Meanwhile, glucose regulation is improving through the use of automated insulin delivery systems that combine glucose monitoring with insulin pumps. New-generation insulins (those that are ultrarapid, ultralong, and glucose-responsive) improve outcomes by minimising blood sugar fluctuations. Together, these breakthroughs offer renewed hope for improving long-term management and quality of life for people living with type 1 diabetes.
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