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肠上皮细胞来源的 CD83 有助于调节性 T 细胞的生成和抑制食物过敏。

Intestinal Epithelial Cell-Derived CD83 Contributes to Regulatory T-Cell Generation and Inhibition of Food Allergy.

机构信息

Department of Gastroenterology, Fifth Hospital of Zhengzhou University, Zhengzhou, China.

Guangdong Provincial Key Laboratory of Regional Immunity and Diseases, Shenzhen, China.

出版信息

J Innate Immun. 2021;13(5):295-305. doi: 10.1159/000515332. Epub 2021 Jun 28.

Abstract

The mechanism of generation of antigen-specific regulatory T cells (Treg) is not fully understood yet. This study aimed to investigate the role of intestinal epithelial cell (IEC)-derived CD83 in the Treg generation in the intestine. In this study, the role of CD83 in the generation of Tregs was assessed in a cell-culture model and a food allergy (FA) mouse model. We found that mouse IECs expressed CD83; its levels were markedly lower in sensitized mice. Mice with CD83-deficient IECs failed to induce Tregs in the intestine. CD83 promoted the transforming growth factor-β-inducible early gene 1 (TIEG1) expression in CD4+ T cells. Toll-like receptor 4 (TLR4)/myeloid differentiation protein-2 (MD-2) complex mediated the effects of CD83 on the expression of TIEG1. Activation of the CD83/TLR4/MD-2/TIEG1 promoted the Treg generation. Concomitant administration of CD83 and specific antigens, but not either one alone, efficiently inhibited experimental FA via inducing the Treg generation in the intestine. In Conclusion, IEC expresses CD83 that is low in sensitized mice. Concomitant administration of CD83 and specific antigens efficiently inhibits FA in a murine model via inducing Tregs in the intestine. The data suggest that CD83 has translation potential in the treatment of FA.

摘要

抗原特异性调节性 T 细胞(Treg)的产生机制尚未完全阐明。本研究旨在探讨肠上皮细胞(IEC)衍生的 CD83 在肠道中 Treg 产生中的作用。在这项研究中,我们在细胞培养模型和食物过敏(FA)小鼠模型中评估了 CD83 在 Treg 产生中的作用。我们发现鼠 IEC 表达 CD83;致敏小鼠的水平明显降低。缺乏 CD83 的 IEC 的小鼠未能在肠道中诱导 Treg。CD83 促进 CD4+T 细胞中转化生长因子-β诱导的早期基因 1(TIEG1)的表达。Toll 样受体 4(TLR4)/髓样分化蛋白 2(MD-2)复合物介导了 CD83 对 TIEG1 表达的影响。CD83/TLR4/MD-2/TIEG1 的激活促进了 Treg 的产生。同时给予 CD83 和特异性抗原,但不是单独给予任何一种,可通过在肠道中诱导 Treg 的产生,有效地抑制实验性 FA。总之,IEC 表达 CD83,致敏小鼠中的 CD83 水平较低。同时给予 CD83 和特异性抗原可通过在肠道中诱导 Treg 来有效抑制 FA。这些数据表明 CD83 在治疗 FA 方面具有转化潜力。

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