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斑点酶联免疫吸附试验和酶联免疫电转印印迹法检测尿液棘球蚴抗原在囊性棘球蚴病诊断中的应用评估

Evaluation of Dot-ELISA and enzyme-linked immuno-electrotransfer blot assays for detection of a urinary hydatid antigen in the diagnosis of cystic echinococcosis.

作者信息

Swarna S R, Parija Subhash Chandra

机构信息

Department of Microbiology, Sree Ramasamy Memorial Medical College Hospital and Research Centre, Potheri, Sri Ramaswamy Memorial University, Kattankulathur, Tamilnadu, India.

出版信息

Trop Parasitol. 2012 Jan;2(1):38-44. doi: 10.4103/2229-5070.97238.

Abstract

BACKGROUND

Several serological assays are used for detection of a hydatid antigen in serum for diagnosis of cystic echinococcosis (CE). However, it requires technical expertise and is associated with the risk of acquiring blood-borne infections. Of late, interests have been shifted to other body fluids like urine, saliva, tear drops as alternate specimens in the diagnosis of CE.

AIM

The aim of the study was to evaluate the dot enzyme-linked immunosorbent assay (Dot-ELISA) and electro-immunotransfer blot (EITB) for detection of a hydatid antigen in the urine for diagnosis of CE.

MATERIALS AND METHODS

100 ml of urine samples were collected from the patients with confirmed CE (n=30), patients with suspected CE (n=30), patients with other diseases (n=30) and healthy controls (n=30). A hydatid antigen in urine was detected by Dot-ELISA and EITB using only polyclonal antibodies raised against a complete homogenate hydatid (CHH) antigen in rabbits.

RESULTS AND CONCLUSIONS

The Dot-ELISA using polyclonal antibodies showed a sensitivity of 53.33% and specificity of 96.66%, whereas EITB showed a sensitivity of 46.66%. The Dot-ELISA and EITB employing polyclonal antibodies showed no significant difference in sensitivity (P=0.426). Hence, the Dot-ELISA being a simple procedure can be used for detection of a hydatid antigen in urine for diagnosis of CE.

摘要

背景

几种血清学检测方法用于检测血清中的棘球蚴抗原,以诊断囊型棘球蚴病(CE)。然而,这需要专业技术,并且存在感染血源性疾病的风险。近来,人们的兴趣已转向其他体液,如尿液、唾液、泪液,作为CE诊断的替代标本。

目的

本研究的目的是评估斑点酶联免疫吸附测定(Dot-ELISA)和电免疫转印印迹法(EITB)用于检测尿液中的棘球蚴抗原以诊断CE。

材料和方法

从确诊为CE的患者(n = 30)、疑似CE的患者(n = 30)、患有其他疾病的患者(n = 30)和健康对照者(n = 30)中收集100 ml尿液样本。仅使用兔抗完整匀浆棘球蚴(CHH)抗原产生的多克隆抗体,通过Dot-ELISA和EITB检测尿液中的棘球蚴抗原。

结果与结论

使用多克隆抗体的Dot-ELISA显示敏感性为53.33%,特异性为96.66%,而EITB显示敏感性为46.66%。使用多克隆抗体的Dot-ELISA和EITB在敏感性上无显著差异(P = 0.426)。因此,Dot-ELISA作为一种简单的方法可用于检测尿液中的棘球蚴抗原以诊断CE。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/935d/3593503/e2e49245c6b3/TP-2-38-g004.jpg

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