期刊文献+

日本血吸虫抗独特型抗体NP30抗体检测法在云南大山区应用效果的评价 被引量:6

Potency of anti-idiotypic antibody NP30/antibody detection for schistosomiasis japonica in mountainous areas in Yunnan Province
下载PDF
导出
摘要 目的评价日本血吸虫抗独特型抗体NP30抗体检测法在云南大山区血吸虫病流行现场的应用效果。方法对云南大山区血吸虫病流行区的506位居民进行粪检,同时用NP30抗体检测法和血吸虫抗体ELISA检测试剂盒(SEA-ELISA)分别对其血清进行检测,评价NP30抗体检测法的敏感性;同时检测非流行区的100份血清确定其特异性。结果NP30抗体检测法和SEA-ELISA法的粪检阳性符合率分别为87.80%(144/164)和84.76%(139/164);两者的特异性分别为96.00%(96/100)和94.00%(94/100),差异均无显著性(P均>0.05),但在粪孵阴性人群血清样本中,NP30抗体检测法和SEA-ELISA法的检出率分别为44.15%(151/342)和70.47%(241/342),差异有显著性(P<0.05)。结论NP30抗体检测法可用于云南大山区血吸虫病筛查。 Objective To evaluate the potency of NP30 antibody detection for the diagnosis of schistosomiasis japonica in the mountainous endemic spots in Yunnan Province. Methods A total of 506 inhabitants in the mountainous schistosomiasis endemic regions of Yunnan Province were examined by using the stool hatching test for parasitological stool examination; the sera samples from 506 villagers were tested with NP30 antibody detection and SEA-ELISA for immune examination respectively, and the sensitivity of NP30 antibody detection was estimated . Their specificity was determined by testing 100 sera from nonepidemic scenes. Results The positive coincidence of stool hatching test with NP30 antibody detection and SEA-ELISA were 87.80% (144/164)and 84.76% (139/164) respectively, and their specificity as 96.00%(96/100)and 94.00%(94/100), with no significant difference between them (P〉0. 05). However, in the negative sera from stool hatching test, the detection rate was 44.15% (151/342) by NP30 antibody detection, and 70. 47%(241/ 342)by SEA-ELISA, the difference was significant(P〈0. 05). Conclusion NP30 could be used in the mountainous area of Yunnan Province for the diagnosis of schistosomiasis japonica.
出处 《中国血吸虫病防治杂志》 CAS CSCD 2006年第3期185-188,共4页 Chinese Journal of Schistosomiasis Control
基金 国家高技术研究发展计划(863计划)(2002AA214181)
关键词 日本血吸虫病 抗独特型抗体 抗体检测 可溶性虫卵抗原-酶联免疫吸附试验 Schistosomiasis japonica Anti-idiotypic Antibody detection SEA-ELISA
  • 相关文献

参考文献9

二级参考文献24

共引文献146

同被引文献61

引证文献6

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部