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Antigen based detection of cystic echinococcosis in buffaloes using ELISA and Dot-EIA.使用酶联免疫吸附测定法(ELISA)和斑点酶免疫测定法(Dot-EIA)基于抗原检测水牛的囊型包虫病。
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Calculation of the ELISA's cut-off based on the change-point analysis method for detection of Trypanosoma cruzi infection in Bolivian dogs in the absence of controls.在缺乏对照的情况下,基于变化点分析方法计算用于检测玻利维亚犬感染克氏锥虫的酶联免疫吸附测定(ELISA)临界值。
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A Study of Cross-Reactivity Between Recombinant EPC1 Antigen of Echinococcus granulosus in Serum from Patients with Confirmed Cystic Echinococcosis Infection and Other Parasitic Infections.泡型棘球蚴病确诊感染患者及其他寄生虫感染患者血清中细粒棘球绦虫重组EPC1抗原交叉反应性的研究
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Sero-epidemiological value of some hydatid cyst antigen in diagnosis of human cystic echinococcosis.某些包虫囊肿抗原在人体囊型棘球蚴病诊断中的血清流行病学价值。
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Evaluation of purified 27.5 kDa protoscolex antigen-based ELISA for the detection of circulating antigens and antibodies in sheep and human hydatidosis.基于纯化的27.5 kDa原头蚴抗原的酶联免疫吸附测定法在检测绵羊和人类包虫病循环抗原及抗体中的应用评估
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动物包虫囊肿基因型作为人包虫囊肿的潜在替代物,作为诊断人畜共患包虫病的抗原来源。

Animal hydatid cyst genotypes as a potential substitute for human hydatid cyst as a source of antigen for diagnosis of zoonotichydatidosis.

作者信息

Ramadan Reem M, Khalifa Marwa M, El-Akkad Dina M, Abdel-Wahab Azza M, El-Bahy Mohamed M

机构信息

Department of Parasitology, Faculty of Veterinary Medicine, Cairo University, Giza, 12211 Egypt.

Department of Parasitology, Faculty of Medicine, Cairo University, Giza, Egypt.

出版信息

J Parasit Dis. 2021 Jun;45(2):424-434. doi: 10.1007/s12639-020-01309-2. Epub 2020 Nov 18.

DOI:10.1007/s12639-020-01309-2
PMID:34295041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8254676/
Abstract

The Diagnosis of hydatidosis is still an unsolved issue due to difficulties in obtaining of patient's hydatid cyst appropriate for antigen extraction. This study evaluated the suitability of HC protoscolices somatic antigens (HCPsS-Ag) fractions from animal origin to substitute that extracted from HC of patients in diagnosis of hydatidosis using enzyme-linked immunoelectro-transfer blot and Enzyme-linked immunosorbent assay (ELISA). Eight fractions in HC-G6 from patients react specifically versus HC-G6 infected patient's sera. Five of them (28, 32, 38, 59 and 89 Kilo Dalton (KDa) and two of them (28 KDa and 45 KDa) reacted versus HC-G1 and HC-G4 infected sheep and equine sera, respectively. Six fractions in HCPsS-Ag-G1 of sheep react versus HC-G1 sheep infected sera, four (28, 32, 52 and 58 KDa) and two of them reacted versus HC-G6 and HC-G4 infected patient and equine sera, respectively. Two fractions only in HCPsS-Ag-G4 of equine reacted versus infected human and sheep sera. This fraction displayed the same degree of ELISA value versus different infected sera with a significantly perfect classification for agreement and non-statistically significant difference ( ≥ 0.05) for ELISA Optical density values of the positive samples without cross-reaction versus other parasites antibodies in sera. HCPsS-Ag from HC genotypes that developed in humans and animals as HC-G6 and HC-G1 can substitute each other for diagnosis of infection than antigens extracted from non-zoonotic HC-G4. The fraction at 28 KDa is the only fraction that can be extracted from any animals HC and used in diagnosis of zoonotic hydatidosis.

摘要

由于难以获取适合抗原提取的患者包虫囊肿,包虫病的诊断仍是一个未解决的问题。本研究使用酶联免疫电转移印迹法和酶联免疫吸附测定法(ELISA),评估了动物源性的包虫原头节体细胞抗原(HCPsS-Ag)组分替代从患者包虫囊肿中提取的抗原用于包虫病诊断的适用性。患者HC-G6中的8个组分与HC-G6感染患者的血清发生特异性反应。其中5个(28、32、38、59和89千道尔顿(KDa))分别与HC-G1和HC-G4感染的绵羊和马血清发生反应。绵羊HCPsS-Ag-G1中的6个组分与HC-G1感染的绵羊血清发生反应,其中4个(28、32、52和58 KDa)分别与HC-G6和HC-G4感染的患者和马血清发生反应。马的HCPsS-Ag-G4中只有2个组分与感染的人和绵羊血清发生反应。该组分对不同感染血清显示出相同程度的ELISA值,对阳性样本的一致性分类显著完美,阳性样本的ELISA光密度值与血清中其他寄生虫抗体无交叉反应且无统计学显著差异(≥0.05)。来自人类和动物体内形成的HC基因型如HC-G6和HC-G1的HCPsS-Ag,在诊断感染时可相互替代,而不是从非人畜共患的HC-G4中提取的抗原。28 KDa的组分是唯一可从任何动物包虫中提取并用于诊断人畜共患包虫病的组分。