Centers for Disease Control and Prevention, Division of Vector-Borne Infectious Diseases, Fort Collins, Colorado, USA.
Am J Trop Med Hyg. 2010 Nov;83(5):1146-55. doi: 10.4269/ajtmh.2010.10-0212.
We evaluated performance of three commercial Japanese encephalitis virus (JEV) IgM antibody capture enzyme-linked immunosorbent assay (MAC ELISA) kits with a panel of serological specimens collected during a surveillance project of acute encephalitis syndrome in India and acute meningitis and encephalitis syndrome in Bangladesh. The serum and cerebral spinal fluid specimens had been referred to the Centers for Disease Control and Prevention (CDC) for confirmatory testing. The CDC results and specimen classifications were considered the reference standard. All three commercial kits had high specificity (95-99.5%), but low sensitivities, ranging from 17-57%, with both serum and cerebrospinal fluid samples. Specific factors contributing to low sensitivity compared with the CDC ELISA could not be determined through further analysis of the limits and dilution end points of IgM detection.
我们评估了三种商业日本脑炎病毒 (JEV) IgM 抗体捕获酶联免疫吸附试验 (MAC ELISA) 试剂盒的性能,这些试剂盒使用了在印度急性脑炎综合征和孟加拉国急性脑膜炎和脑炎综合征监测项目中收集的血清学标本。血清和脑脊液标本已被送往疾病控制和预防中心 (CDC) 进行确认检测。CDC 的检测结果和标本分类被视为参考标准。所有三种商业试剂盒的特异性都很高(95-99.5%),但敏感性较低,血清和脑脊液标本的范围为 17-57%。与 CDC ELISA 相比,导致敏感性较低的具体因素无法通过进一步分析 IgM 检测的限值和稀释终点来确定。