Lin Shan, Ma Zhanchuan, Huang Yuanping, Sun Yu, Yi Huanfa
Central Laboratory, The First Hospital of Jilin University, Changchun, Jilin, 130031, China; Department of Respiratory Medicine, The First Hospital of Jilin University, Changchun, Jilin, 130031, China.
Central Laboratory, The First Hospital of Jilin University, Changchun, Jilin, 130031, China.
Mol Immunol. 2022 Jan;141:87-93. doi: 10.1016/j.molimm.2021.11.007. Epub 2021 Nov 24.
Chronic obstructive pulmonary disease (COPD) is characterized by a progressive, persistent immune response to cigarette smoke, and it has been suggested that immune dysregulation is involved in its pathogenesis. A subset of regulatory B cells (Bregs) with high levels of the surface markers CD24 and CD38 (CD24CD38) has previously been shown to exert an immunosuppressive function. This study investigated the levels and activity of CD24CD38 Bregs in stable COPD (sCOPD). Testing the peripheral blood from 65 patients with sCOPD and 39 control subjects for CD24CD38 Breg subsets by flow cytometry showed that the patients with sCOPD had significantly lower levels of CD24CD38 Bregs and IL-10 B cells. The patients with sCOPD had lower serum interleukin-10 levels than the controls. The patients with most severe sCOPD had the lowest levels of CD24CD38 Bregs. Spearman correlation analysis showed that the levels of CD24CD38 Bregs in the patients with sCOPD positively correlated with serum interleukin-10 concentrations but not with levels of C-reactive protein. Compared to healthy controls, functional studies showed that Breg cells from patients with sCOPD exhibit a decreased suppressive function. We conclude that sCOPD is characterized by the exhaustion of CD24CD38 regulatory B cells compartment. Therefore, CD24CD38 Bregs may contribute to the pathogenesis of sCOPD.
慢性阻塞性肺疾病(COPD)的特征是对香烟烟雾产生进行性、持续性免疫反应,并且有人提出免疫失调参与其发病机制。先前已表明,具有高水平表面标志物CD24和CD38(CD24⁺CD38⁺)的调节性B细胞(Bregs)亚群具有免疫抑制功能。本研究调查了稳定期COPD(sCOPD)患者中CD24⁺CD38⁺ Bregs的水平和活性。通过流式细胞术检测65例sCOPD患者和39例对照受试者外周血中的CD24⁺CD38⁺ Breg亚群,结果显示sCOPD患者的CD24⁺CD38⁺ Bregs和IL-10⁺ B细胞水平显著降低。sCOPD患者的血清白细胞介素-10水平低于对照组。最严重sCOPD患者的CD24⁺CD38⁺ Bregs水平最低。Spearman相关性分析表明,sCOPD患者的CD24⁺CD38⁺ Bregs水平与血清白细胞介素-10浓度呈正相关,但与C反应蛋白水平无关。与健康对照相比,功能研究表明sCOPD患者的Breg细胞抑制功能降低。我们得出结论,sCOPD的特征是CD24⁺CD38⁺调节性B细胞池耗竭。因此,CD24⁺CD38⁺ Bregs可能参与sCOPD的发病机制。