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用于人类并殖吸虫病血清学诊断的酶联免疫吸附测定法的开发。

Development of enzyme-linked immunosorbent assay for serodiagnosis of human paragonimiasis.

作者信息

Narain Kanwar, Devi K Rekha, Mahanta J

机构信息

Regional Medical Research Centre, N.E. Region (ICMR), Dibrugarh, Assam, India.

出版信息

Indian J Med Res. 2005 Jun;121(6):739-46.

Abstract

BACKGROUND & OBJECTIVE: Although human paragonimiasis is known to occur in Manipur and Arunachal Pradesh, there is no indigenous immunodiagnostic test available in India. Sputum examination for detection of eggs is less sensitive method for diagnosis of paragonimiasis and unfortunately, the eggs are not always present in the sputum of infected individuals. Due to overlapping clinical manifestations and similarities between X-ray picture in pulmonary paragonimiasis and pulmonary tuberculosis, chances of diagnostic confusion can increase. Therefore, the objective of this study was to develop an ELISA test indigenously for diagnosis of paragonimiasis.

METHODS

Somatic (S) and excretory-secretory (ES) antigens of adult trematodes belonging to genus Paragonimus were prepared. Serum samples were collected from 22 confirmed patients of paragonimiasis and from five groups of negative controls. The cut-off points for both types of antigens were calculated using receiver operating characteristic (ROC) curve analysis. The sensitivity, specificity, predictive values and efficiency of the ELISA tests were also calculated.

RESULTS

IgG-ELISA test using either S or ES antigens were 100 per cent sensitive yet the utility of S antigen for diagnosis of paragonimiasis seemed to be less reliable because of low specificity (91.3%). On the other hand, ES antigen was more reliable with 100 per cent specificity as no false positive cases were recorded.

INTERPRETATION & CONCLUSION: ES antigen can be effectively used for screening large populations for paragonimiasis. In areas where both paragonimiasis and tuberculosis are endemic, suspected subjects should be screened for both the diseases because of chance of mistaken diagnosis. Correct diagnosis will avoid unnecessary costly treatment.

摘要

背景与目的

虽然已知印度曼尼普尔邦和阿鲁纳恰尔邦有人感染并殖吸虫病,但印度尚无本土免疫诊断检测方法。通过痰液检查虫卵来诊断并殖吸虫病的方法敏感性较低,而且不幸的是,受感染个体的痰液中并不总是存在虫卵。由于并殖吸虫病的临床表现与肺结核的X线影像存在重叠和相似之处,诊断混淆的可能性会增加。因此,本研究的目的是自主研发一种用于诊断并殖吸虫病的酶联免疫吸附测定(ELISA)检测方法。

方法

制备了并殖吸虫属成年吸虫的体抗原(S)和排泄分泌抗原(ES)。从22例确诊的并殖吸虫病患者以及五组阴性对照中采集血清样本。使用受试者工作特征(ROC)曲线分析计算两种抗原的临界值。还计算了ELISA检测的敏感性、特异性、预测值和效率。

结果

使用S抗原或ES抗原的IgG-ELISA检测敏感性均为100%,但由于特异性较低(91.3%),S抗原在诊断并殖吸虫病中的效用似乎不太可靠。另一方面,ES抗原更可靠,特异性为100%,因为未记录到假阳性病例。

解读与结论

ES抗原可有效用于大规模人群的并殖吸虫病筛查。在并殖吸虫病和结核病都流行的地区,由于存在误诊的可能性,对疑似患者应同时进行这两种疾病的筛查。正确诊断将避免不必要的昂贵治疗。

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