Wang Bing, Bai Wenmei, Ma Hongxia, Li Fengsen
Department of Pulmonary Medicine, Xinjiang Medical University, Urumqi, Xinjiang, China (mainland).
Department of Pulmonary Medicine, Traditional Chinese Medicine Hospital Affiliated to Xinjiang Medical University, Urumqi, Xinjiang, China (mainland).
Med Sci Monit. 2021 Jan 2;27:e927577. doi: 10.12659/MSM.927577.
BACKGROUND Idiopathic pulmonary fibrosis (IPF) is a serious irreversible lung disease. The mechanism of immune checkpoint in idiopathic pulmonary fibrosis is still unknown. MATERIAL AND METHODS First, the expression levels of PD-1/PD-L1 on the surface of CD4+ T cells and the proportion of Treg cells in IPF or controls were detected by flow cytometry. Then, expression of TGF-ß in blood samples was detected with ELISA. Moreover, a co-culture system was composed of fibroblasts stimulated by TGF-ß and CD4+ T cells from healthy people. The proportions of Treg cells and PD-1 in the co-culture system were detected. In addition, we detected the proportion of Treg cells and the level of collagen-1 after adding PD-1 or PD-L1 protein antibody blocker to the co-culture system. RESULTS Flow cytometry revealed the upregulated expression of PD-1/PD-L1 in CD4+ T cells of IPF patients. PD-1 appears to inhibit the differentiation of CD4+ T cells into Treg cells. Co-culture of myofibroblasts and CD4+ T cells induced the generation of collagen-1 and reduced the proliferation of CD4+ T cells. When PD-1 was blocked, the inhibition of Treg cell differentiation was reversed, accompanied by decreased collagen-1 production. CONCLUSIONS This work identified the molecular mechanism of PD-1 in patients with IPF. It may provide a new perspective on the therapeutic effect of PD-1.
特发性肺纤维化(IPF)是一种严重的不可逆性肺部疾病。特发性肺纤维化中免疫检查点的机制仍不清楚。
首先,通过流式细胞术检测IPF患者或对照组中CD4+T细胞表面PD-1/PD-L1的表达水平以及Treg细胞的比例。然后,用ELISA检测血样中TGF-β的表达。此外,构建了由TGF-β刺激的成纤维细胞与健康人CD4+T细胞组成的共培养体系。检测共培养体系中Treg细胞和PD-1的比例。另外,在共培养体系中加入PD-1或PD-L1蛋白抗体阻断剂后,检测Treg细胞的比例和胶原蛋白-1的水平。
流式细胞术显示IPF患者CD4+T细胞中PD-1/PD-L1表达上调。PD-1似乎抑制CD4+T细胞向Treg细胞的分化。肌成纤维细胞与CD4+T细胞共培养诱导了胶原蛋白-1的生成并减少了CD4+T细胞的增殖。当阻断PD-1时,Treg细胞分化的抑制被逆转,同时胶原蛋白-1的产生减少。
本研究确定了IPF患者中PD-1的分子机制。它可能为PD-1的治疗效果提供新的视角。