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作 者:梁劲松[1] 胡振斌[2] 梁中夏 农朝赞[4] 农茜茜
机构地区:[1]广西中医药大学第一附属医院检验科,广西南宁510405 [2]广西中医药大学第一附属医院肝病科,广西南宁510405 [3]广西医科大学 [4]广西壮族自治区民族医院 [5]右江民族医学院
出 处:《胃肠病学和肝病学杂志》2014年第11期1312-1314,共3页Chinese Journal of Gastroenterology and Hepatology
基 金:广西卫生厅自然科学基金(Z20110822)
摘 要:目的探讨慢性乙型肝炎病毒(HBV)感染患者血浆HBV DNA载量与乙肝血清标志物的关系及与白细胞介素2(IL-2)、白细胞介素6(IL-6)、白细胞介素8(IL-8)、白细胞介素13(IL-13)含量变化的相关性。方法选取60例慢性HBV感染者(疾病组),采用免疫发光法定量检测乙型肝炎标志物;实时荧光定量PCR(FQ-PCR)检测HBV DNA载量,并以<5.0×102copies/ml为临界点分为高载量组、低载量组;酶联免疫吸附试验(ELISA)检测IL-2、IL-6、IL-8、IL-13含量;并与20名健康对照者(正常对照组)比较。结果疾病组血浆HBV DNA载量<5.0×102copies/ml时,以HBs Ag、抗-HBe、抗-HBc 3项指标升高为主要表现,阳性检出率为95%,IL-2、IL-6、IL-8、IL-13水平显著高于正常对照组(P<0.05);血浆HBV DNA>5.0×102copies/ml时,以HBs Ag、HBe Ag、抗-HBc 3项指标升高为主要表现,疾病组阳性检出率为70%,抗-HBe阳性检出率为30%;疾病组血清IL-2、IL-6、IL-8、IL-13水平显著高于对照组(P<0.05),并显著高于血浆HBV DNA低载量组(P<0.05)。结论 HBV DNA载量和细胞因子水平的变化可反应机体免疫活动状况,对临床观察疗效具有重要意义。Objective To investigate the plasma of patients with chronic hepatitis B virus (HBV) infection of HBV DNA loads and the relationship between hepatitis B serum marker and IL-2,IL-6,IL-8,IL-13 content.Methods Sixty patients with chronic HBV infection (disease group).Hepatitis B markers were detected by immune luminescence assay HBV DNA loads was detected by real-time quantitative PCR (FQ-PCR),and < 5.0 × 102copies/ml for the critical point was divided into two groups:high load group and low load group.The IL-2,IL-6,IL-8,IL-13 content were detected by enzyme-linked immunosorbent assay (ELISA).And compared with 20 cases of healthy controls (control group).Results HBV DNA < 5.0 × 102 copies/ml in disease group,with HBsAg,anti-HBe,anti-HBc indexes increased as the main performance,the positive rate was 95%,IL-2,IL-6,IL-8,IL-13 levels in serum were significantly higher than those in control group (P <0.05).The plasma HBV DNA > 5.0 × 102copies/ml,with HBsAg,HBeAg,anti-HBc indexes increased as the main performance,the positive detection rate was 70%,anti-HBe positive rate was 30%.The serum levels of IL-2,IL-6,IL 8,IL-13 were significantly higher than those in control group (P < 0.05),and significantly higher than the low load group (P < 0.05).Conclusion HBV DNA load and changes in cytokine levels can response the body' s immune activity,which is of great significance for the clinical treatment.
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