Arnold V, Balkow S, Staats R, Matthys H, Luttmann W, Virchow J C
Pneumologische Abteilung, Medizinischen Universitätsklinik Freiburg, Deutschland.
Pneumologie. 2000 Oct;54(10):468-73. doi: 10.1055/s-2000-7690.
The cause of asthma which has been linked to a chronic, T-cell-mediated bronchial inflammation, remains unclear. A number of other T-lymphocyte-mediated, chronic inflammatory disorders have been associated with autoimmunity and there are data indicating that autoimmune phenomena might also be present in asthma. Expression of perforin, a cytotoxic molecule produced by lymphocytes, has been implicated in the pathogenesis of autoimmune disease. We therefore tested the hypothesis that allergic and intrinsic asthma might be associated with an increase in lymphocytes producing perforin by comparing the expression of intracellular perforin in peripheral blood lymphocytes of patients with extrinsic asthma (n = 13), intrinsic asthma (n = 7), and healthy (control subjects (n = 18). Lymphocytes were identified using flow cytometry and subdivided into CD3(+), CD4(+), CD8(+), CD16(+), and CD56(+) subpopulations after staining with appropriate monoclonal antibodies. The percentage of perforin-positive total lymphocytes as significantly elevated in patients with allergic as well as intrinsic asthma when compared with normal control subjects. Analysis of lymphocyte subpopulations also revealed a significant increase in the percentage of CD3(+), CD4(+), CD8(+), and CD56(+) cells expressing perforin in allergic asthma and a significant increase in the percentage of CD4(+), and CD56(+) cells in intrinsic asthma when compare with healthy control subjects. Perforin expression in CD4(+) cells in intrinsic asthma was also significantly elevated compared with allergic asthma. We conclude that allergic and intrinsic asthma is associated with increased expression of perforin in T-lymphocyte subsets.
哮喘的病因与慢性T细胞介导的支气管炎症有关,但其确切病因仍不清楚。许多其他T淋巴细胞介导的慢性炎症性疾病与自身免疫有关,并且有数据表明哮喘中也可能存在自身免疫现象。淋巴细胞产生的细胞毒性分子穿孔素的表达与自身免疫性疾病的发病机制有关。因此,我们通过比较外源性哮喘患者(n = 13)、内源性哮喘患者(n = 7)和健康对照者(n = 18)外周血淋巴细胞中细胞内穿孔素的表达,来检验过敏性哮喘和内源性哮喘可能与产生穿孔素的淋巴细胞增加有关这一假设。使用流式细胞术鉴定淋巴细胞,并用适当的单克隆抗体染色后,将其细分为CD3(+)、CD4(+)、CD8(+)、CD16(+)和CD56(+)亚群。与正常对照者相比,过敏性哮喘和内源性哮喘患者中穿孔素阳性总淋巴细胞的百分比显著升高。淋巴细胞亚群分析还显示,与健康对照者相比,过敏性哮喘中表达穿孔素的CD3(+)、CD4(+)、CD8(+)和CD56(+)细胞百分比显著增加,内源性哮喘中CD4(+)和CD56(+)细胞百分比显著增加。与过敏性哮喘相比,内源性哮喘中CD4(+)细胞中的穿孔素表达也显著升高。我们得出结论,过敏性哮喘和内源性哮喘与T淋巴细胞亚群中穿孔素表达增加有关。