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:王飙[1] 赵和平[1] 于燕[1] 陈伯伦[1] 王林川[2]
机构地区:[1]西安交通大学附属红会医院检验科,西安710054 [2]西安交通大学第一附属医院检验科,西安710061
出 处:《现代检验医学杂志》2013年第4期74-75,共2页Journal of Modern Laboratory Medicine
摘 要:目的 探讨血清白细胞介素-2(IL-2),白细胞介素-6 (IL-6)在丙型肝炎患者体内的变化及临床意义.方法 对临床确诊65例丙型肝炎(其中25例慢性丙肝,21例丙肝肝硬化,19例丙肝肝癌患者)和20例健康人群采用酶联免疫吸附法(ELISA)进行血清IL-2,IL-6水平的检测.结果 慢性丙肝、肝硬化、肝癌和正常人群IL-2,IL-6水平(pg/ml)分别为:51.64±2.34,40.43±2.47,30.64±2.43,87.38±1.93;33.78±4.17,40.54±2.66,45.49±1.81,27.75±1.99.与正常人群比较,丙型肝炎(40.90±2.41 pg/ml)患者血清IL-2水平是降低的(t=13.23,P〈0.05);IL-6的水平(36.60±2.88 pg/ml)是升高的(t=9.27,P〈0.05).其中血清IL-2水平随着病情的进展而降低(慢性丙肝组〉肝硬化组〉肝癌组,t=3.98,P〉0.05);而IL-6含量随着病情的进展而升高(t=2.38,P〈0.01).结论 IL-2和IL-6水平变化与丙肝致肝硬化和癌变有关.Objective To analyse the clinical significance of changes of serum IL-2,IL-6 (interleukin-2,interleukin-6) in pa- tientswith hepatitis C. Methods Detected the levers of IL-2 and IL-6 by using enzyme-linked immunosorbent assay (ELISA) in 65 patients with clinically diagnosed hepatitis C (including 25 patients with chronic hepatitis C,21 patients with liver cir- rhosis,liver cancer 19 cases) and 20 cases of healthy people. Results The levers of IL-2 and IL-6 in chronic hepatitis C,liver cirrhosis,liver cancer, healthy people were 51.64± 2.34 pg/ml, 40. 43 ±2.47 pg/ml, 30.64±2.43 pg/ml, 87.38 ±1.93 pg/ ml; 33. 78± 4. 17 pg/ml, 40. 54 ± 2.66 pg/ml, 45.49 ± 1.81 pg/ml, 27.75 ±1.99 pg/ml, respectively. Compared with the normal population,patients with hepatitis C serum IL-2 levels were reduced(t = 13.23, P〈0.05) and IL-6 levels were ele- vated (t= 9.27, P〈0. 05). The levels of serum IL-2 decreased as the disease progresses (CHC〉cirrhosis〉 HCC,t= 3.98, P〉0.05). The levels of IL-6 increased as the disease progresses (t=2.38,P〈0.01). Conclusion The IL-2 and IL-6 chan- ges associated with HCV cause liver fibrosis and cancer.
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:216.73.216.195