Laboratory of Nano- and Translational Medicine, Carolina Center for Cancer Nanotechnology Excellence, Carolina Institute of Nanomedicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Department of Radiation Oncology, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Adv Mater. 2021 Jun;33(25):e2101253. doi: 10.1002/adma.202101253. Epub 2021 May 8.
Type 1 diabetes mellitus (T1DM) is a chronic autoimmune disease that results from autoreactive T cells destroying insulin-producing pancreatic beta (β) cells. The development of T1DM is associated with the deficiency of co-inhibitory immune checkpoint ligands (e.g., PD-L1, CD86, and Gal-9) in β cells. Here, a new translational approach based on metabolic glycoengineering and bioorthogonal click chemistry, which bioengineers β cells with co-inhibitory immune checkpoint molecules that induce antigen-specific immunotolerance and reverse early-onset hyperglycemia is reported. To achieve this goal, a subcutaneous injectable acellular pancreatic extracellular matrix platform for localizing the bioengineered β cells while creating a pancreas-like immunogenic microenvironment, in which the autoreactive T cells can interface with the β cells, is devised.
1 型糖尿病(T1DM)是一种慢性自身免疫性疾病,由自身反应性 T 细胞破坏产生胰岛素的胰腺β(β)细胞引起。T1DM 的发展与β细胞中协同抑制性免疫检查点配体(如 PD-L1、CD86 和 Gal-9)的缺乏有关。在这里,报告了一种基于代谢糖基工程和生物正交点击化学的新转化方法,该方法通过生物工程β细胞表达协同抑制性免疫检查点分子,诱导抗原特异性免疫耐受并逆转早期高血糖。为了实现这一目标,设计了一种皮下可注射的非细胞性胰腺细胞外基质平台,用于定位生物工程化的β细胞,同时创建一个类似胰腺的免疫原性微环境,使自身反应性 T 细胞能够与β细胞相互作用。