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Type 1 diabetes induced by immune checkpoint inhibitors

机译:由免疫检查点抑制剂诱导的1型糖尿病

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摘要

With the increasing use of immune checkpoint inhibitors (ICI) including anti-cytotoxic T lymphocyte associated antigen-4 (CTLA-4) and anti-programmed cell death-1 (PD-1) in cancers, ICI-induced type 1 diabetes has been reported throughout the world. In this review, we aim to summarize the characteristics of this disease and discuss the mechanism of it. As an immune-related adverse event, type 1 diabetes developed after the administration of anti-PD-1 or anti-PD-ligand 1 (PD-L1) in the combination with or without anti-CTLA-4. It usually presented with acute onset, and 62.1% of the reported cases had diabetic ketoacidosis. Only a third of them had positive autoantibodies associated with type 1 diabetes. Susceptible HLA genotypes might be associated. T-cell-stimulation by blocking of the interaction of PD-1 and PD-L1 in pancreatic β cells was the main mechanism involved in the pathology. Insulin was the only effective treatment of ICI-induced type 1 diabetes. In conclusions, ICI-induced type 1 diabetes is a potentially life-threating adverse event after the immunotherapy of cancers. Screening and early recognition is important. Further investigation of the mechanism may help to better understand the pathology of type 1 diabetes.
机译:随着免疫检查点抑制剂(ICI)的增加,包括抗细胞毒性T淋巴细胞相关抗原-4(CTLA-4)和癌症中的反编程细胞死亡-1(PD-1),ICI诱导的1型糖尿病在全世界报道。在本综述中,我们的目标是总结该疾病的特征,并讨论它的机制。作为免疫相关的不良事件,在与或不含抗CTLA-4的组合后,在施用抗PD-1或抗PD-LigAnd 1(PD-L1)后发育1型糖尿病。它通常呈急性发作,报告病例的62.1%具有糖尿病酮症症。其中只有三分之一具有与1型糖尿病相关的阳性自身抗体。可能有关易感HLA基因型。通过阻断PD-1和PD-L1在胰腺β细胞中的相互作用的T细胞刺激是病理学中涉及的主要机制。胰岛素是ICI诱导的1型糖尿病的唯一有效治疗方法。总之,ICI诱导的1型糖尿病是癌症免疫治疗后的潜在危及生命的不良事件。筛选和早期识别很重要。进一步调查机制可能有助于更好地理解1型糖尿病的病理学。

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