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一种非侵入性口腔液检测法在以感染HIV为主的人群中检测梅毒螺旋体IgG的应用。

Application of a noninvasive oral fluid test for detection of treponemal IgG in a predominantly HIV-infected population.

作者信息

Maple P A C, Simms I, Kafatos G, Solomou M, Fenton K

机构信息

Health Protection Agency South West Laboratory, Myrtle Road, Kingsdown, Bristol BS2 8EL, UK.

出版信息

Eur J Clin Microbiol Infect Dis. 2006 Dec;25(12):743-9. doi: 10.1007/s10096-006-0216-x.

Abstract

The performance of a time-resolved fluorescence immunoassay (TRFIA) for detection of treponemal IgG from oral fluid specimens has been assessed in a predominantly HIV-infected population. Serological investigation is the method of choice for confirming clinical suspicion of syphilis; however, in the primary stage of disease, direct detection of treponemes in lesion fluid or Treponema pallidum DNA is recommended because of the reduced sensitivity of serological tests. There may be occasions when blood for serological investigation is difficult to obtain due to individual patient preference or logistical necessity to improve participation in screening initiatives, particularly in outreach situations. Collection of oral fluid for detection of treponemal antibody may prove an attractive alternative and, with this in mind, an oral fluid assay for detection of treponemal IgG was developed. Time-resolved fluorescence was used to detect treponemal IgG extracted from commercially available oral fluid collection devices. Paired serum and saliva samples were obtained from 210 individuals, 101 of whom were diagnosed with syphilis on the grounds of medical examination confirmed by serological testing. Oral fluid specimens from 14 subjects were rejected because they contained insufficient control antibody or were inhibitory. The population tested was predominantly men who have sex with men, many of whom were HIV infected. The overall sensitivity and specificity of the oral fluid assay was 95.8 and 86.1%, respectively, based on the 5th percentile of the positive results, and 93.7 and 91.1%, respectively, based on a cutoff derived by mixture model analysis. For individuals with primary syphilis, the optimum sensitivity of the oral fluid assay was 87.5%, whereas in those with disease classified as secondary syphilis and early latent syphilis, the sensitivity of the oral fluid assay was 100 and 94.7%, respectively. The oral fluid assay is a useful alternative to serological testing in certain situations, and further development of this technology to enable detection of treponemal IgM should increase its sensitivity for detecting cases of primary syphilis.

摘要

在以感染艾滋病毒者为主的人群中,对用于检测口腔液标本中梅毒螺旋体IgG的时间分辨荧光免疫分析法(TRFIA)的性能进行了评估。血清学调查是确诊梅毒临床疑似病例的首选方法;然而,在疾病的一期,由于血清学检测的敏感性降低,建议直接检测病损处液体中的梅毒螺旋体或梅毒螺旋体DNA。由于患者个人偏好或为提高筛查项目参与度而出于后勤需要,有时难以获取用于血清学调查的血液,尤其是在开展外展服务的情况下。收集口腔液用于检测梅毒螺旋体抗体可能是一种有吸引力的替代方法,考虑到这一点,开发了一种用于检测梅毒螺旋体IgG的口腔液检测法。采用时间分辨荧光法检测从市售口腔液采集装置中提取的梅毒螺旋体IgG。从210名个体中获取了配对的血清和唾液样本,其中101人经血清学检测确诊为梅毒。来自14名受试者的口腔液标本被拒收,因为它们所含的对照抗体不足或具有抑制作用。接受检测的人群主要是男男性行为者,其中许多人感染了艾滋病毒。基于阳性结果的第5百分位数,口腔液检测法的总体敏感性和特异性分别为95.8%和86.1%,基于混合模型分析得出的临界值,分别为93.7%和91.1%。对于一期梅毒患者,口腔液检测法的最佳敏感性为87.5%,而在被分类为二期梅毒和早期潜伏梅毒的患者中,口腔液检测法的敏感性分别为100%和94.7%。在某些情况下,口腔液检测法是血清学检测的一种有用替代方法,进一步开发该技术以能够检测梅毒螺旋体IgM应可提高其对一期梅毒病例的检测敏感性。

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