Vaughn D W, Nisalak A, Solomon T, Kalayanarooj S, Nguyen M D, Kneen R, Cuzzubbo A, Devine P L
United States Army Medical Component-Armed Forces Research Institute of Medical Science, Bangkok, Thailand.
Am J Trop Med Hyg. 1999 Apr;60(4):693-8. doi: 10.4269/ajtmh.1999.60.693.
A commercial capture ELISA for specific IgM and IgG antibodies produced during dengue infection (PanBio Dengue Duo) showed excellent sensitivity (99%, n = 78) using sera collected at hospital discharge compared with established ELISA and hemagglutination inhibition (HAI) assays. Furthermore, the ELISA was able to diagnose 79% of the dengue cases using sera collected at hospital admission. The ELISA also showed high specificity (92%) in paired sera from patients without flavivirus infection (n = 26), although 45% of the patients with Japanese encephalitis (n = 20) showed elevation of IgG but not IgM. The IgG capture ELISA showed good correlation with the HAI assay (r = 0.83, P < 0.0001), and IgG levels could be used to distinguish between primary and secondary infection, with 100% of primary infections and 96% of secondary infections being correctly classified. This ELISA should prove useful in the clinical diagnosis of dengue infections.
一种用于检测登革热感染期间产生的特异性IgM和IgG抗体的商业捕获ELISA(泛生物登革热双抗检测试剂盒),与既定的ELISA和血凝抑制(HAI)试验相比,使用出院时采集的血清显示出极佳的灵敏度(99%,n = 78)。此外,该ELISA使用入院时采集的血清能够诊断79%的登革热病例。在没有黄病毒感染的患者的配对血清中(n = 26),该ELISA也显示出高特异性(92%),不过45%的日本脑炎患者(n = 20)显示IgG升高但IgM未升高。IgG捕获ELISA与HAI试验显示出良好的相关性(r = 0.83,P < 0.0001),并且IgG水平可用于区分原发性和继发性感染,100%的原发性感染和96%的继发性感染被正确分类。这种ELISA在登革热感染的临床诊断中应会被证明是有用的。