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基于重组抗原Ss-NIE-1的粪类圆线虫病免疫诊断检测方法的开发。

Development of Ss-NIE-1 recombinant antigen based assays for immunodiagnosis of strongyloidiasis.

作者信息

Rascoe Lisa N, Price Courtney, Shin Sun Hee, McAuliffe Isabel, Priest Jeffrey W, Handali Sukwan

机构信息

Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Emory College, Emory University, Atlanta, Georgia, United States of America.

出版信息

PLoS Negl Trop Dis. 2015 Apr 10;9(4):e0003694. doi: 10.1371/journal.pntd.0003694. eCollection 2015 Apr.

Abstract

Strongyloides stercoralis is a widely distributed parasite that infects 30 to 100 million people worldwide. In the United States strongyloidiasis is recognized as an important infection in immigrants and refugees. Public health and commercial reference laboratories need a simple and reliable method for diagnosis of strongyloidiasis to identify and treat cases and to prevent transmission. The recognized laboratory test of choice for diagnosis of strongyloidiasis is detection of disease specific antibodies, most commonly using a crude parasite extract for detection of IgG antibodies. Recently, a luciferase tagged recombinant protein of S. stercoralis, Ss-NIE-1, has been used in a luciferase immunoprecipitation system (LIPS) to detect IgG and IgG4 specific antibodies. To promote wider adoption of immunoassays for strongyloidiasis, we used the Ss-NIE-1 recombinant antigen without the luciferase tag and developed ELISA and fluorescent bead (Luminex) assays to detect S. stercoralis specific IgG4. We evaluated the assays using well-characterized sera from persons with or without presumed strongyloidiasis. The sensitivity and specificity of Ss-NIE-1 IgG4 ELISA were 95% and 93%, respectively. For the IgG4 Luminex assay, the sensitivity and specificity were 93% and 95%, respectively. Specific IgG4 antibody decreased after treatment in a manner that was similar to the decrease of specific IgG measured in the crude IgG ELISA. The sensitivities of the Ss-NIE-1 IgG4 ELISA and Luminex assays were comparable to the crude IgG ELISA but with improved specificities. However, the Ss-NIE-1 based assays are not dependent on native parasite materials and can be performed using widely available laboratory equipment. In conclusion, these newly developed Ss-NIE-1 based immunoassays can be readily adopted by public health and commercial reference laboratories for routine screening and clinical diagnosis of S. stercoralis infection in refugees and immigrants in the United States.

摘要

粪类圆线虫是一种广泛分布的寄生虫,全球约有3000万至1亿人受其感染。在美国,粪类圆线虫病被认为是移民和难民中的一种重要感染病。公共卫生和商业参考实验室需要一种简单可靠的粪类圆线虫病诊断方法,以识别和治疗病例并防止传播。公认的粪类圆线虫病诊断实验室检测方法是检测疾病特异性抗体,最常用的是使用粗制寄生虫提取物检测IgG抗体。最近,一种带有荧光素酶标签的粪类圆线虫重组蛋白Ss-NIE-1已被用于荧光素酶免疫沉淀系统(LIPS)中,以检测IgG和IgG4特异性抗体。为了促进更广泛地采用粪类圆线虫病免疫测定法,我们使用了不带荧光素酶标签的Ss-NIE-1重组抗原,并开发了酶联免疫吸附测定(ELISA)和荧光微球(Luminex)测定法来检测粪类圆线虫特异性IgG4。我们使用来自疑似患有或未患有粪类圆线虫病患者的特征明确的血清对这些测定法进行了评估。Ss-NIE-1 IgG4 ELISA的敏感性和特异性分别为95%和93%。对于IgG4 Luminex测定法,敏感性和特异性分别为93%和95%。治疗后特异性IgG4抗体下降,其方式与粗制IgG ELISA中测得的特异性IgG下降相似。Ss-NIE-1 IgG4 ELISA和Luminex测定法的敏感性与粗制IgG ELISA相当,但特异性有所提高。然而,基于Ss-NIE-1的测定法不依赖于天然寄生虫材料,并且可以使用广泛可用的实验室设备进行。总之,这些新开发的基于Ss-NIE-1的免疫测定法可被公共卫生和商业参考实验室轻松采用,用于美国难民和移民中粪类圆线虫感染的常规筛查和临床诊断。

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