Department of Respiratory Medicine, Shizuoka General Hospital, and Hamamatsu University School of Medicine, Shizuoka, Japan.
Allergol Int. 2010 Mar;59(1):75-82. doi: 10.2332/allergolint.09-OA-0126. Epub 2009 Dec 25.
Recent studies suggest that Tc1/Tc2 imbalances are implicated in the pathogenesis of chronic obstructive pulmonary disease (COPD). The purpose of this study was to clarify the relationship between peripheral blood T-cell profiles and pulmonary function or inflammatory parameters.
Thirty-one patients with stable COPD (median age 70 years, 30 males, 15 current smokers and 16 ex-smokers) and 30 healthy control subjects were enrolled in this study. The subjects underwent blood tests, exhaled nitric oxide (eNO) measurement, pulmonary function tests, and sputum induction. Tc1/Tc2 and Th1/Th2 were determined by analyzing intracellular cytokine staining for IFN-gamma and IL-4 in peripheral blood CD8+ and CD4+ T cells using flow cytometry after stimulation with phorbol 12-myristate 13-acetate and ionomycin.
There was a significantly increased proportion of IFN-gamma-producing and IL-4-producing CD8+ T cells in patients with COPD compared with control subjects (median [IQR] 73.6% [63.9%-80.7%] vs 62.0% [45.6%-73.8%], p=0.004; and 2.6% [1.1%-6.9%] vs 1.1% [0.6%-2.2%], p=0.002, respectively). In addition, the proportion of IFN-gamma-producing CD4+ T cells was significantly higher in patients with COPD compared with control subjects (25.7% [21.2%-38.0%] vs 22.8% [15.6%-29.2%], p=0.027). The proportion of IFN-gamma-producing CD8+ T cells was correlated negatively with single-breath carbon monoxide transfer coefficient (Kco)(rho=-0.45, p=0.033) and positively with eNO (rho=0.50, p=0.012). The proportion of IL-4-producing CD8+ T cells was positively correlated with body mass index (rho=0.42, p=0.023) and Kco (rho=0.47, p=0.026).
It is suggested that Tc1 cells have a detrimental role and that Tc2 cells have a protective role in disease progression.
最近的研究表明,Tc1/Tc2 失衡与慢性阻塞性肺疾病(COPD)的发病机制有关。本研究的目的是阐明外周血 T 细胞谱与肺功能或炎症参数之间的关系。
纳入 31 例稳定期 COPD 患者(中位年龄 70 岁,30 名男性,15 名现吸烟者和 16 名曾吸烟者)和 30 名健康对照者。对受试者进行血液检查、呼出气一氧化氮(eNO)测量、肺功能检查和痰诱导。通过分析 PMA 和离子霉素刺激后外周血 CD8+和 CD4+T 细胞中 IFN-γ和 IL-4 的细胞内细胞因子染色,使用流式细胞术确定 Tc1/Tc2 和 Th1/Th2。
与对照组相比,COPD 患者 IFN-γ产生和 IL-4 产生的 CD8+T 细胞比例显著增加(中位数[IQR]73.6%[63.9%-80.7%] vs 62.0%[45.6%-73.8%],p=0.004;2.6%[1.1%-6.9%] vs 1.1%[0.6%-2.2%],p=0.002)。此外,COPD 患者 IFN-γ产生的 CD4+T 细胞比例也明显高于对照组(25.7%[21.2%-38.0%] vs 22.8%[15.6%-29.2%],p=0.027)。IFN-γ产生的 CD8+T 细胞比例与单呼气一氧化碳传递系数(Kco)呈负相关(rho=-0.45,p=0.033),与 eNO 呈正相关(rho=0.50,p=0.012)。IL-4 产生的 CD8+T 细胞比例与体重指数(rho=0.42,p=0.023)和 Kco(rho=0.47,p=0.026)呈正相关。
提示 Tc1 细胞具有有害作用,Tc2 细胞在疾病进展中具有保护作用。