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一种用于检测麻风分枝杆菌酚糖脂-I抗体的简易试纸检测法。

A simple dipstick assay for the detection of antibodies to phenolic glycolipid-I of Mycobacterium leprae.

作者信息

Bührer S S, Smits H L, Gussenhoven G C, van Ingen C W, Klatser P R

机构信息

Department of Biomedical Research, Royal Tropical Institute, Amsterdam, The Netherlands.

出版信息

Am J Trop Med Hyg. 1998 Feb;58(2):133-6. doi: 10.4269/ajtmh.1998.58.133.

Abstract

Among the many reported applications of the detection of antibodies to phenolic glycolipid-I (PGL-I) of Mycobacterium leprae, in particular, the use of seroprevalence as an indicator of the magnitude of the leprosy problem may turn out to be very useful in leprosy control programs. An operational function of serology within the leprosy control services requires a simple test system. We have developed a simple dipstick assay for the detection of antibodies to PGL-I and compared its performance with that of an ELISA. A high degree of agreement (97.2%) was observed between the ELISA and the dipstick assay when tested on 435 sera; the agreement beyond chance (Kappa value) was 0.92. No significant difference was found between the dipstick assay and the ELISA when seropositivity rates obtained in groups of leprosy patients, household contacts, and controls were compared. The interpretation of the dipstick results as positive or negative was unequivocal, as illustrated by the high agreement between different persons reading the test (Kappa values > 0.88). Storage of the only reagents required, the dipsticks and the stabilized detection reagent, up to three weeks under tropical conditions of high temperatures, high humidity, and exposure to light, did not influence the results of the assay. The dipstick assay described here is an easy-to-perform method for the detection of IgM antibodies to PGL-I of M. leprae; it does not require any special equipment and the highly stable reagents make the test robust and suitable for use in tropical countries. An internal control validates the performance of the assay. This dipstick assay may be the method of choice for epidemiologic mapping of leprosy.

摘要

在众多已报道的检测麻风分枝杆菌酚糖脂-I(PGL-I)抗体的应用中,特别是将血清流行率用作麻风问题严重程度的指标,可能在麻风控制项目中非常有用。麻风控制服务中血清学的一项实用功能需要一个简单的检测系统。我们开发了一种用于检测PGL-I抗体的简单试纸条检测法,并将其性能与酶联免疫吸附测定(ELISA)法进行了比较。在对435份血清进行检测时,ELISA法与试纸条检测法之间观察到高度一致性(97.2%);超出偶然的一致性(kappa值)为0.92。比较麻风患者组、家庭接触者组和对照组的血清阳性率时,试纸条检测法与ELISA法之间未发现显著差异。试纸条检测结果判断为阳性或阴性明确无误,不同人员读取检测结果之间的高度一致性(kappa值>0.88)就说明了这一点。所需的唯一试剂试纸条和稳定化检测试剂,在高温、高湿度和光照的热带条件下储存长达三周,并不影响检测结果。本文所述的试纸条检测法是一种检测麻风分枝杆菌PGL-I IgM抗体的易于操作的方法;它不需要任何特殊设备,高度稳定的试剂使检测可靠且适用于热带国家。内部对照可验证检测的性能。这种试纸条检测法可能是麻风病流行病学绘图的首选方法。

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