摘要
用酶联免疫吸附试验(ELISA)、斑点酶联免疫吸附试验(Dot一ELISA)和斑点免疫金银染色(Dot一IGSS)同步检测50份班氏微丝蚴血症者血清中抗丝虫IgG。ELISA、Dot一ELISA和Dot一IGSS检测抗体阳性率分别为86%(43/50)、90%(45/50)和100%(50/50)。ELISA和Dot一ELISA联合应用阳性率为96%(48/50)。ELISA与Dot一IGSS检测微丝蚴血症者抗体阳性率有显著性差异(P<0.05),抗体阳性率在ELISA与Dot一ELISA、Dot一ELIISA与Dot一IGSS之间则无显著性差异。三种方法所检测的抗体强度与外周血中微丝蚴密度无相关关系。
Enzyme一linked immunosorbent assay(ELISA ),dot一ELISA and Dot一immuno gold silverstaining(Dot一IGSS) were used to detect the specific IgG against filaria in sera collected from 50 bancroftianmicrofilaremia cases simultaneously. The positive rate was 86%(43/50), 90%(45/5) and l00%(50/50)withELISA,Dot一ELISA and Dot一IGSS respectively. The positive rate was 96%(48/50) when ELISA and Doot一ELISA were combined. There was a significant difference between the results detected with Dot-IGSS andELISA(P<0. 05) and there were no statistically significant differences between ELISA and Dot一ELISA andbetween Dot一ELISA and Dot-IGSS respectively. There was no correlation between the microfilaria densityand the specific antibody level detected by the three serologic tests.
出处
《地方病通报》
1995年第2期39-41,共3页
Endemic Diseases Bulletin
关键词
班氏微丝蚴血症
血清学
丝虫病
免疫诊断
Bancroftian microfilaremia
Serology
Enzyme一linked immunosorbent assay
Dot一enzyme一linked immunorbent assay
Dot一immunogold silver staining