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作 者:刘英杰[1] 刘云[1] 曲耀华[1] 郑勇[2] 刘艳红 张永利[4] 陈娟
机构地区:[1]河南大学医学院细胞与分子免疫学实验室,开封475001 [2]河南大学第一附属医院,河南开封475001 [3]开封市防疫站,开封475000 [4]河南大学附属淮河医院,开封475000
出 处:《中国寄生虫学与寄生虫病杂志》2003年第6期342-344,共3页Chinese Journal of Parasitology and Parasitic Diseases
摘 要:目的 研究应用斑点免疫金渗滤法 (DIGFA)快速检测旋毛虫病患者血清抗旋毛虫IgG抗体。 方法 采用旋毛虫肌肉期幼虫膜抗原 ,以胶体金颗粒结合的羊抗人IgG为标记抗体 ,以颜色深浅为判断阳性标准。 结果 纯化的旋毛虫肌肉期幼虫膜抗原与患者血清中特异性抗旋毛虫IgG抗体通过渗滤在硝酸纤维素膜上反应 ,1 0min内即可直接观察结果。在 76份患者血清的检测中 ,阳性率为 94 .74 % ,与ELISA法的检出阳性率 86 .84 %相比差异无显著性 ( χ2 =2 .83,P >0 .0 5)。交叉试验与重复试验结果显示DIGFA具有较好的特异性及稳定性。Objective To study a new quick method for detecting serum IgG against Trichinella spiralis (T.s). Methods Membrane antigen of muscle larva of T.s was isolated and combined with the nitrocellulose membrane. Goat anti-human IgG was conjugated with the golden pellets of colloidal state which was used as marked antibody for the experiment of dot-immunogold filtration assay to examine specific IgG. Results T.s IgG and its corresponding antigen reacted on the membrane by filtration, and the result could be observed with naked eyes within 10 min. In the examination of 76 clinical serum samples, the positive rate was (94.7%). It was not significantly higher than that of ELISA(χ~2=2.83,P>0.05). Conclusion The dot-immunogold filtration assay is rapid and simple for performing and reading in the detection of IgG against T.s with high sensitivity and specificity.
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