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使用单克隆抗体通过酶联免疫吸附抑制试验对囊尾蚴病进行血清学诊断。

Serodiagnosis of cysticercosis by ELISA-inhibition test using monoclonal antibodies.

作者信息

Yong T S, Yeo I S, Seo J H, Chang J K, Lee J S, Kim T S, Jeong G H

机构信息

Department of Parasitology, Yonsei University College of Medicine, Seoul, Korea.

出版信息

Korean J Parasitol. 1993 Jun;31(2):149-56. doi: 10.3347/kjp.1993.31.2.149.

DOI:10.3347/kjp.1993.31.2.149
PMID:8343457
Abstract

Monoclonal antibodies (Mabs) were produced against crude scolex extract of T. solium metacestodes, and applied to ELISA-inhibition test for improving the specificity of serodiagnosis of human cysticercosis. Four hybridomas secreting species-specific anticysticercal Mabs (Cya-1, Cya-7, Cya-28 and Cya-31) were selected. Each Mab reacted on antigenic components of 25.5 kDa (Cya-1), 28 kDa (Cya-7), 87.5 kDa (Cya-28), and 12.5 kDa (Cya-31). IFA showed that Cya-1 was located at the calcium corpuscles, and Cya-7 at the loose connective tissue of T. solium metacestode scolex. Cya-28 and Cya-31 reacted on the tegument of the scolex. By conventional ELISA, 23 out of 28 (82.1%) cysticercosis patients were found serologically positive, but 1 out of 9 (11.1%) sparganosis cases and 6 out of 31 (19.4%) paragonimiasis cases showed false positives. By ELISA-inhibition test using species-specific anti-cysticercal Mab Cya-7, 19 out of 28 (67.9%) cysticercosis cases were found serologically positive, but there were no false positives in other parasitic infections.

摘要

制备了针对猪带绦虫囊尾蚴粗头节提取物的单克隆抗体,并将其应用于酶联免疫吸附抑制试验,以提高人体囊尾蚴病血清诊断的特异性。筛选出了4株分泌种特异性抗囊尾蚴单克隆抗体(Cya-1、Cya-7、Cya-28和Cya-31)的杂交瘤。每株单克隆抗体分别与25.5 kDa(Cya-1)、28 kDa(Cya-7)、87.5 kDa(Cya-28)和12.5 kDa(Cya-31)的抗原成分发生反应。间接荧光抗体试验显示,Cya-1定位于钙颗粒,Cya-7定位于猪带绦虫囊尾蚴头节的疏松结缔组织。Cya-28和Cya-31对头节的皮层发生反应。采用常规酶联免疫吸附试验,28例囊尾蚴病患者中有23例(82.1%)血清学呈阳性,但9例裂头蚴病患者中有1例(11.1%)和31例肺吸虫病患者中有6例(19.4%)出现假阳性。采用种特异性抗囊尾蚴单克隆抗体Cya-7进行酶联免疫吸附抑制试验,28例囊尾蚴病患者中有19例(67.9%)血清学呈阳性,而其他寄生虫感染均未出现假阳性。

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A case of extensive spinal cysticercosis involving the whole spinal canal in a patient with a history of cerebral cysticercosis.
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Yonsei Med J. 2009 Aug 31;50(4):582-4. doi: 10.3349/ymj.2009.50.4.582. Epub 2009 Aug 19.