Hamzaoui Agnès, Kahan Alice, Ayed Khaled, Hamzaoui Kamel
Department of Paediatric and Respiratory Diseases, A. Mami Hospital, Aciana, Tunisia.
Mediators Inflamm. 2002 Apr;11(2):113-9. doi: 10.1080/09629350220131971.
T lymphocytes have a central regulatory role in the pathogenesis of asthma. The objective of this study was to characterize immunologically the activation stage of asthma and the functional profile of lymphocytes from induced sputum, with particular emphasis on gammadelta T cells.
Induced sputum was collected from 10 patients with acute exacerbation of asthma, and from healthy controls. The expression of activation markers on freshly isolated induced sputum lymphocytes and T-cell subsets was analyzed by double immunofluorescent staining and flow cytometry. Fas ligand (FasL) was determined by reverse transcriptase-polymerase chain reaction analysis. The phenotype of gammadelta T-cell subpopulations was tested by A13 and BB3 monoclonal antibodies. In this context, the functional profile of gammadelta T cells was tested in a chromium releasing test.
A significantly decreased proportion of alphabeta T cells and an increased proportion of gammadelta T cells, CD56+ cells and CD8+ gammadelta T cells were found in asthma patients compared with healthy controls. In asthmatic patients, there is a significantly increased proportion of T cells expressing CD69 and CD25 antigen. After stimulation of gammadelta T cells, an increased expression of intracellular tumour necrosis factor-alpha, interleukin (IL)-4 and IL10 cytokines were found at higher levels than controls. Interferon-gamma was observed at similar levels in asthma patients and healthy controls. Freshly isolated T-cell receptor (TCR) gammadelta+ cells exhibited an increased percentage of FasL in our patient group. FasL mRNA was detected in TCR gammadelta+ cells before and after IL2 stimulation. TCR gammadelta+ cells were cytotoxic against the K562 cell line. This natural killer activity was mediated by the A13-positive subpopulation.
The presence of cytokines producing gammadelta cells in induced sputum of asthmatic patients is consistent with regulatory activities. These cells display also cytotoxic function.
T淋巴细胞在哮喘发病机制中起核心调节作用。本研究的目的是从免疫学角度对哮喘的激活阶段以及诱导痰中淋巴细胞的功能特征进行表征,尤其着重于γδT细胞。
从10例哮喘急性加重患者及健康对照者中收集诱导痰。通过双免疫荧光染色和流式细胞术分析新鲜分离的诱导痰淋巴细胞及T细胞亚群上激活标志物的表达。采用逆转录聚合酶链反应分析测定Fas配体(FasL)。用A13和BB3单克隆抗体检测γδT细胞亚群的表型。在此背景下,在铬释放试验中检测γδT细胞的功能特征。
与健康对照相比,哮喘患者中αβT细胞比例显著降低,γδT细胞、CD56 +细胞及CD8 +γδT细胞比例增加。在哮喘患者中,表达CD69和CD25抗原的T细胞比例显著增加。γδT细胞受到刺激后,细胞内肿瘤坏死因子-α、白细胞介素(IL)-4和IL10细胞因子的表达高于对照组。哮喘患者和健康对照者中干扰素-γ水平相似。在我们的患者组中,新鲜分离的T细胞受体(TCR)γδ +细胞表现出FasL百分比增加。在IL2刺激前后,TCRγδ +细胞中均检测到FasL mRNA。TCRγδ +细胞对K562细胞系具有细胞毒性。这种自然杀伤活性由A13阳性亚群介导。
哮喘患者诱导痰中存在产生细胞因子的γδ细胞,这与调节活性一致。这些细胞还具有细胞毒性功能。