Idali F, Wahlström J, Müller-Suur C, Eklund A, Grunewald J
Karolinska Institutet, Department of Medicine, Unit of Respiratory Medicine, Stockholm, Sweden.
Clin Exp Immunol. 2008 Apr;152(1):127-37. doi: 10.1111/j.1365-2249.2008.03609.x. Epub 2008 Feb 14.
In pulmonary sarcoidosis, the typical T helper 1-mediated immune response in the lungs has been proposed to be co-ordinated by regulatory T cells; however, their exact role needs to be clarified. We used real-time polymerase chain reaction to study genes involved in regulatory T cell functions in CD4+ T cells isolated from bronchoalveolar lavage fluid (BALF) of patients (n = 24) and healthy subjects (n = 7). The genes included the transcription factor forkhead box P3 (FoxP3), interleukin (IL)-10, transforming growth factor-beta1 and chemokine receptor 2 (CCR2). The same genes were also studied in isolated BALF CD4+ T cell receptor AV2S3+ and AV2S3(-) T cells of patients with lung-restricted AV2S3 T cell expansions (n = 12). Intracellular staining of the FoxP3 protein was performed additionally in 14 patients and nine healthy subjects. mRNA expression of FoxP3, CCR2 and IL-10 was decreased significantly in BALF CD4+ T cells of patients. Flow cytometric analysis of CD4+ T cells also demonstrated a decreased frequency of FoxP3+ cells in the BALF and blood of sarcoidosis patients as well as a reduced intensity (mean fluorescence intensity) of FoxP3 expression in BALF FoxP3+ cells of patients. BALF CD4+AV2S3+ T cells expressed significantly lower levels of FoxP3 and CCR2 mRNA versus BALF CD4+AV2S3- T cells. The main conclusion of our study is that there is a reduced expression of regulatory T cell associated genes in BALF CD4+ T cells in sarcoidosis. In addition, our data suggest an effector function of AV2S3+ lung-accumulated T cells in sarcoidosis.
在肺结节病中,肺部典型的辅助性T细胞1介导的免疫反应被认为是由调节性T细胞协调的;然而,它们的确切作用尚需阐明。我们使用实时聚合酶链反应研究从患者(n = 24)和健康受试者(n = 7)的支气管肺泡灌洗液(BALF)中分离出的CD4 + T细胞中与调节性T细胞功能相关的基因。这些基因包括转录因子叉头框P3(FoxP3)、白细胞介素(IL)-10、转化生长因子-β1和趋化因子受体2(CCR2)。在患有肺部局限性AV2S3 T细胞扩增的患者(n = 12)的分离BALF CD4 + T细胞受体AV2S3 +和AV2S3(-)T细胞中也研究了相同的基因。另外对14例患者和9名健康受试者进行了FoxP3蛋白的细胞内染色。患者BALF CD4 + T细胞中FoxP3、CCR2和IL-10的mRNA表达显著降低。对CD4 + T细胞的流式细胞术分析还显示,结节病患者的BALF和血液中FoxP3 +细胞的频率降低,以及患者BALF FoxP3 +细胞中FoxP3表达的强度(平均荧光强度)降低。与BALF CD4 + AV2S3- T细胞相比,BALF CD4 + AV2S3 + T细胞表达的FoxP3和CCR2 mRNA水平显著降低。我们研究的主要结论是,结节病患者BALF CD4 + T细胞中调节性T细胞相关基因的表达降低。此外,我们的数据表明结节病中AV2S3 +肺聚集性T细胞具有效应功能。