Yu Biqing, Yang Xiaohong, Li Fengsen, Wu Chao, Wang Wenyi, Ding Wei
Xinjiang Medical University, Urumqi, China; Department of Respiratory and Critical Care Medicine, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, China.
Bosn J Basic Med Sci. 2017 Feb 21;17(1):17-22. doi: 10.17305/bjbms.2016.1233.
Pigeon breeder's lung (PBL) is a type of lung inflammatory disease associated with the immune response to repeated pigeon-derived antigen exposure. The pathogenesis of PBL remains unclear. In this study, peripheral blood samples were collected from Uygur acute - and chronic-phase PBL patients and healthy subjects with pigeon contact. Foxp3+CD4+ regulatory T cell (Treg) activity in different phases of PBL was characterized by changes in Foxp3+CD4+ Treg, CD4+CD25+ T cell, and T lymphocyte subsets. Based on hypersensitivity pneumonitis (HP) diagnosis criteria, 32 PBL cases from January 2012 to December 2013 in the People's Hospital of Xinjiang Uygur Autonomous Region Respiratory Department were included. Lung high-resolution computed tomography was performed, and the cases were classified based on the HP phase into 15 acute-phase and 17 chronic-phase cases. The control group included 30 healthy subjects with Uygur pigeon contact. Blood samples were collected, and the T cell subsets were analyzed via flow cytometry. In both PBL groups, the Foxp3+CD4+ Treg and CD4+CD25+ and CD4+CD3+ T cell percentages and CD4+/CD8+ ratios were significantly lower than in the control group (p < 0.01). In the PBL groups, particularly the acute-phase group, the CD8+CD3+ T lymphocyte percentage was significantly higher than in the control group (p < 0.01). There were no significant differences in CD4+CD25+ cells between the PBL groups. In peripheral blood from the PBL groups, the CD4+/CD8+ ratio was positively correlated with the Foxp3+CD4+ Treg (r = 0.864, p < 0.05) and CD4+/CD25+ cell (r = 0.34, p < 0.05) percentages. Low Foxp3+CD4+ Treg expression or overconsumption may be a pathogenic factor in PBL.
鸽饲养者肺(PBL)是一种与反复接触鸽源抗原后的免疫反应相关的肺部炎症性疾病。PBL的发病机制尚不清楚。在本研究中,收集了维吾尔族PBL急性期和慢性期患者以及有鸽接触史的健康受试者的外周血样本。通过Foxp3 + CD4 +调节性T细胞(Treg)、CD4 + CD25 + T细胞和T淋巴细胞亚群的变化来表征PBL不同阶段的Treg活性。根据过敏性肺炎(HP)诊断标准,纳入了2012年1月至2013年12月在新疆维吾尔自治区人民医院呼吸科的32例PBL病例。进行了肺部高分辨率计算机断层扫描,并根据HP阶段将病例分为15例急性期和17例慢性期病例。对照组包括30名有鸽接触史的维吾尔族健康受试者。采集血样,通过流式细胞术分析T细胞亚群。在两个PBL组中,Foxp3 + CD4 + Treg、CD4 + CD25 +和CD4 + CD3 + T细胞百分比以及CD4 + /CD8 +比值均显著低于对照组(p < 0.01)。在PBL组中,特别是急性期组,CD8 + CD3 + T淋巴细胞百分比显著高于对照组(p < 0.01)。PBL组之间CD4 + CD25 +细胞无显著差异。在PBL组的外周血中,CD4 + /CD8 +比值与Foxp3 + CD4 + Treg(r = 0.864,p < 0.05)和CD4 + /CD25 +细胞(r = 0.34,p < 0.05)百分比呈正相关。低Foxp3 + CD4 + Treg表达或过度消耗可能是PBL的致病因素。