检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:刘芳[1] 唐婷玉[1] 杜坚宗[1] 钦光跃[1]
出 处:《全科医学临床与教育》2016年第4期382-384,共3页Clinical Education of General Practice
摘 要:目的探讨特发性肺纤维化(IPF)患者外周血中T淋巴细胞亚群和相关细胞因子的变化。方法选取35例IPF患者(IPF组)和38例健康体检人员(对照组),分别采用流式细胞技术及酶联免疫吸附法检测外周血CD3+、CD4+、CD8+T细胞百分率及血清干扰素γ(IFN-γ)、白介素(IL)-2、IL-4、IL-13的水平。结果 IPF组患者外周血CD3+、CD4+淋巴细胞亚群及CD4+/CD8+比值与对照组比较明显下降,CD8+明显增加,差异均有统计学意义(t分别=5.65、3.06、-6.10、3.35,P均<0.05)。IPF组患者外周血中IFN-γ和IL-2水平明显低于对照组,IL-4和IL-13水平明显高于对照组,差异均有统计学意义(t分别=6.13、4.03、-5.38、-8.28,P均<0.05)。结论 IPF患者外周血T淋巴细胞亚群及相关细胞因子发生变化,提示存在免疫系统紊乱,免疫机制可能参与了IPF的发病并在其中发挥重要作用。Objective To explore the changes of T lymphocytes subset and related lymphocytes cytokine in peripheral blood mononuclear cells of patients with idiopathic pulmonary fibrosis(IPF). Methods Thirty-five patients with IPF and38 healthy volunteers were selected to detect the percentages of CD^3+, CD^4+, CD^8+T lymphocytes in the peripheral blood mononuclear cells by enzyme linked immunosorbent assay(ELISA) and the levels of interferon-γ(IFN-γ),interleukin(IL)-2,IL-4,IL-13 in the blood serum by flow cytometry(FCM). Results The lymphocytes subset(CD^3+, CD^4+) and the ratio of CD^4+/CD^8+in IPF group were significantly lower than those in the control group while the level of CD^8+in IPF group was significantly higher(t=5.65,3.06,-6.10,3.35,P〈0.05). The level of IFN-γ and IL-2 in IPF group were significantly lower than those in the control group,while levels of IL-4 and IL-13 in IPF group were significantly higher than those in the control group(t=6.13,4.03,-5.38,-8.28,P〈0.05). Conclusion The changes of T lymphocytes subset and related lymphocytes cytokine in peripheral blood mononuclear cells of patients with idiopathic pulmonary fibrosis indicate that the im-mune system may participate in and play an important role in pathogenesis of the IPF.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.194