Xiang Xiao, Tianping Wang, Zhigang Tian
Institute of Immunology, School of Life Sciences, University of Science and Technology of China, 443 Huangshan Road, Hefei, Anhui 230027, China.
J Immunol Methods. 2003 Sep;280(1-2):49-57. doi: 10.1016/s0022-1759(03)00196-0.
The colloidal dye immunofiltration assay (CDIFA) combines the concepts of the double-antigen sandwich assay, the Dot immunofiltration assay, and colloidal dye-linked antigen technique to produce a new dye immunoassay for antibody detection in schistosomiasis. The CDIFA consisted of soluble egg antigen (SEA) of Schistosoma japonicum coated onto nitrocellulose membrane, mounted on a flow-through test device to provide the assay capture matrix. SEA absorbed to a red colloidal dye, R-3, produced in China, served as the antigen-antibody complex detecting reagents. The results showed that the sensitivity of the CDIFA was 100% in 35 cases of acute schistosomiasis (35/35), 98% in 50 cases of chronic schistosomiasis (49/50). The specificity of the assay was 99.4% in 180 healthy individuals (179/180). The cross-reaction was 13.3% in 30 cases of paragonimiasis, 2.6% in 38 cases of clonorchiasis sinensis and 0% in 20 cases of hookworm infection, 20 cases of fasciolopsiasis and 16 cases of ascariasis. The results were similar to those detected by routine enzyme-linked immunosorbent assay (ELISA). In a field evaluation of the CDIFA kit, the positivity rate of the CDIFA was 97.5% in 157 cases of schistosomiasis, compared with 91.1% with the circumoval precipitin test (COPT). The dye-labeled SEA conjugate was stable at room temperature for at least 6 months. The results indicated that the CDIFA provided an economic, simple, rapid, robust test for the detection of schistosome infection, suitable for a wide variety of field applications without any instrumentation.
胶体染料免疫渗滤试验(CDIFA)结合了双抗原夹心试验、斑点免疫渗滤试验和胶体染料标记抗原技术的概念,开发出一种用于检测血吸虫病抗体的新型染料免疫分析法。CDIFA由包被在硝酸纤维素膜上的日本血吸虫可溶性虫卵抗原(SEA)组成,该膜安装在流通式检测装置上作为检测捕获基质。吸附了中国产红色胶体染料R-3的SEA用作抗原抗体复合物检测试剂。结果显示,CDIFA对35例急性血吸虫病患者的检测灵敏度为100%(35/35),对50例慢性血吸虫病患者的检测灵敏度为98%(49/50)。该检测方法对180名健康个体的特异性为99.4%(179/180)。30例肺吸虫病患者的交叉反应率为13.3%,38例华支睾吸虫病患者的交叉反应率为2.6%,20例钩虫感染、20例姜片吸虫病和16例蛔虫病患者的交叉反应率为0%。结果与常规酶联免疫吸附试验(ELISA)检测结果相似。在对CDIFA试剂盒的现场评估中,157例血吸虫病患者中CDIFA的阳性率为97.5%,而环卵沉淀试验(COPT)的阳性率为91.1%。染料标记的SEA结合物在室温下至少可稳定保存6个月。结果表明,CDIFA为血吸虫感染检测提供了一种经济、简便、快速、可靠的检测方法,适用于各种无需任何仪器设备的现场应用。