首页> 外文期刊>European journal of clinical microbiology and infectious diseases: Official publication of the European Society of Clinical Microbiology >Application of a noninvasive oral fluid test for detection of treponemal IgG in a predominantly HIV-infected population.
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Application of a noninvasive oral fluid test for detection of treponemal IgG in a predominantly HIV-infected population.

机译:非侵入性口腔液测试在检测主要感染HIV的人群中检测螺旋体IgG的应用。

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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 collectiondevices. 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.
机译:在主要感染HIV的人群中,已经评估了时间分辨荧光免疫分析(TRFIA)从口腔液标本中检出螺旋体IgG的性能。血清学检查是确认梅毒临床怀疑的首选方法。然而,在疾病的初期,由于血清学检测的敏感性降低,建议直接检测病灶液或梅毒螺旋体DNA中的色氨酸。有时候,由于个人患者的偏爱或后勤需要以提高对筛查计划的参与度,尤其是在外展情况下,难以获得用于血清学检查的血液。收集口腔液用于检测螺旋体抗体可能证明是一种有吸引力的替代方法,考虑到这一点,因此开发了一种用于检测螺旋体IgG的口腔液测定方法。时间分辨荧光用于检测从市售口腔液收集装置中提取的螺旋体IgG。配对的血清和唾液样本来自210名个体,其中101名是通过血清学检查证实的医学检查被诊断为梅毒。来自14位受试者的口腔液标本被拒绝,因为它们的对照抗体不足或具有抑制性。测试的人群主要是与男性发生性关系的男性,其中许多人感染了艾滋病毒。基于阳性结果的第5个百分位数,口服液测定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%。对于患有原发性梅毒的个体,口服液检测的最佳敏感性为87.5%,而在那些被归为继发性梅毒和早期潜伏梅毒的疾病中,口服液检测的敏感性分别为100和94.7%。在某些情况下,口服液测定是血清学检测的一种有用的替代方法,该技术的进一步发展使得能够检测梅毒IgM,应提高其检测原发性梅毒病例的敏感性。

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