特发性肺纤维化患者IL-6水平与T细胞功能的检测 |
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作者单位: | Dept. of Respiratory Diseases,The second Clinical College |
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摘 要: | 采用生物活性检测法,观察特发性肺纤维化(IPF)患者外周血单个核细胞(PBMC)自泌白细胞介素6(IL-6)水平及白细胞分化抗原3(CD3)单克隆抗体(McAb)诱导下的T细胞功能。结果表明:IPF患者IL-6自泌水平明显高于正常对照组(P<0.001);在体外CD3McAb诱导下,IPF患者T细胞对抗原免疫应答能力与T细胞在体内的活化过程大致相符,且对IL-6分泌呈异常高表达。提示IL-6分泌水平与IPF病情相关。
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关 键 词: | 特发性肺纤维化 白细胞介素6 T细胞 白细胞分化抗原3单克隆抗体 |
Detection of IL-6 level and T cell's functions in patients with idopathic pulmonary fibrosis |
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Authors: | An Jihong Cheng Guanghui Zhang Jie |
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Abstract: | We observed the self-secretion IL-6 levels of peripheral blood monocytes and T cell's functions induced by CO3McAb in the patients with IPF by means of the bioassay. The results are asfollows: 1. The self-secretion IL-6 levels remarkably increased in the IPF cases than those of controls. (P<0. 001) 2. The immune responses induced by antigen in the patients with IPF matched theactivated process of T cell in vitro, The results suggested that the secretion level of IL-6 might correlate with lPF condition. |
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Keywords: | IPF IL- 6 T-Cell CO_3McAb |
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