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作 者:徐华[1] 韩金祥[1] 高雪芹[1] 刘灿兰[2] 李钿[3] 黄海燕[1] 潘继红[1]
机构地区:[1]山东省医药生物技术研究中心国家卫生部生物技术药物重点实验室,山东济南250062 [2]泰安市中心医院 [3]山东省立医院
出 处:《山东医药》2006年第14期4-5,共2页Shandong Medical Journal
基 金:山东省科技厅资助项目(003100104)
摘 要:目的 探讨蛋白芯片技术检测自身抗体的临床价值。方法 用酶联免疫吸附试验(ELISA)、蛋白芯片法检测抗dsDNA、抗Ro-60/SSA、抗Ro-52/SSA、抗SSB、抗Jo-1、抗磷脂IgG抗体.用间接免疫荧光法(IIF)、蛋白芯片法检测抗核抗体(ANA),分别统计两种方法检测均阳性、均阴性和单阳性的标本数目.并进行评价。结果 芯片法检测ANA的灵敏度为89%、特异度为60%.芯片法对其他6种自身抗体检测的灵敏度为70.0%~87.5%、特异度为92.7%~98.9%。结论 蛋白芯片法检测自身抗体与常规方法比较,特异度较高,有待进一步改善技术提高其灵敏度。Objective: To evaluate the sensitivity and speciality of protein chip technology in the detection of antoantibody and discuss its value in clinical application. Methods: The ANA was detected with indirect immunofluorescence(IIF) and protein chip respectively, and the other six autoantibodies including anti-dsDNA, anti-Ro-60/SSA, anti-Ro-52/SSA, anti-SSB, anti-Jo-1,and anti-phospholipid IgG were simultaneously detected with ELISA and protein chip technology, and numbers of the both positive, both negative and the single positive were analyzed respectively. Results: Compared with IIF in detecting ANA, sensitivity and specificity of the microarray is 89% and 60%; Compared with ELISA in detecting other six autoantibodies, sensitivity and specificity of the microarray is 70. 0% to 87. 5% and 92. 7% to 98. 9%. Conclusion: Compared with routine methods in detecting autoantibodies, protein chip technology has good speciality and its sensitivity should be raised by improving the technology.
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