Chaicumpa W, Ybanez L, Kitikoon V, Pungpak S, Ruangkunaporn Y, Chongsa-nguan M, Sornmani S
Department of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Int J Parasitol. 1992 Jul;22(4):527-31. doi: 10.1016/0020-7519(92)90155-e.
Detection of Opisthorchis viverrini antigens in stools using specific monoclonal antibody. International Journal for Parasitology 22: 527-531. A sandwich enzyme-linked immunosorbent assay (ELISA) was developed for detecting Opisthorchis viverrini antigen in faecal extracts of four groups of individuals. These were 24 patients with O. viverrini infection only (group 1), 31 patients with O. viverrini and other parasitic infections (group 2), 141 patients with other parasitic infections (group 3) and 21 normal, parasite-free individuals (group 4). The first antibody used in the ELISA was polyclonal immunoglobulin G prepared from the serum of a rabbit previously immunized with crude extract of O. viverrini. The second antibody was monoclonal antibody specific to an antigen located in the worm tegument and muscular tissue. Sensitivity of the assay was 31% while specificity was 100%. Considerations for improving the sensitivity are discussed.
使用特异性单克隆抗体检测粪便中华支睾吸虫抗原。《国际寄生虫学杂志》22: 527 - 531。开发了一种夹心酶联免疫吸附测定法(ELISA),用于检测四组个体粪便提取物中的华支睾吸虫抗原。这四组分别为:仅感染华支睾吸虫的24例患者(第1组)、同时感染华支睾吸虫和其他寄生虫的31例患者(第2组)、感染其他寄生虫的141例患者(第3组)以及21名正常、无寄生虫感染的个体(第4组)。ELISA中使用的第一抗体是由先前用华支睾吸虫粗提物免疫的兔血清制备的多克隆免疫球蛋白G。第二抗体是针对位于虫体体表和肌肉组织中的一种抗原的单克隆抗体。该测定法的灵敏度为31%,特异性为100%。文中讨论了提高灵敏度的相关考量因素。