Sirisinha S, Chawengkirttikul R, Sermswan R, Amornpant S, Mongkolsuk S, Panyim S
Faculty of Science, Mahidol University, Bangkok, Thailand.
Am J Trop Med Hyg. 1991 Feb;44(2):140-5. doi: 10.4269/ajtmh.1991.44.140.
Monoclonal antibody-based enzyme-linked immunosorbent assay and DNA hybridization techniques were developed and evaluated for their potential in the detection of Opisthorchis viverrini infection in humans. A mixture of three IgG1 monoclonal antibodies (MAb) specific for the 89 kDa metabolic product of O. viverrini was captured on a microtiter plate by rabbit anti-mouse IgG and used in a sandwich ELISA for the detection of parasite antigen. The 89 kD component bound to the MAb was detected with biotinylated rabbit IgG antibody to O. viverrini metabolic products. As little as 0.05-0.1 ng of the antigen could be detected by this technique. A specific O. viverrini DNA probe constructed from a repetitive DNA segment containing 340 base pairs was used in a dot blot hybridization for the detection of parasite DNA. The labeled probe constructed as such could detect DNA released from as few as five O. viverrini eggs. Both methods were specific for O. viverrini and their sensitivity was comparable with that of the classical parasitological technic.
基于单克隆抗体的酶联免疫吸附测定法和DNA杂交技术被开发并评估了其在检测人体华支睾吸虫感染方面的潜力。三种针对华支睾吸虫89 kDa代谢产物的IgG1单克隆抗体(MAb)混合物通过兔抗小鼠IgG捕获在微量滴定板上,并用于夹心ELISA检测寄生虫抗原。用生物素化的兔抗华支睾吸虫代谢产物IgG抗体检测与MAb结合的89 kD成分。该技术可检测低至0.05 - 0.1 ng的抗原。由包含340个碱基对的重复DNA片段构建的特异性华支睾吸虫DNA探针用于斑点印迹杂交检测寄生虫DNA。如此构建的标记探针可检测低至五个华支睾吸虫卵释放的DNA。这两种方法对华支睾吸虫均具有特异性,其灵敏度与经典寄生虫学技术相当。