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Study of FTA-CFS test using monospecific anti-immunoglobulin conjugates IgG IgM and IgA

机译:使用单特异性抗免疫球蛋白结合物IgGIgM和IgA进行FTA-CFS测试的研究

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摘要

The fluorescent treponemal antibody test for cerebrospinal fluid (FTA-CSF) using monospecific conjugates anti-IgG, IgM, and IgA was used to determine the presence of anti-treponemal antibodies in the spinal fluid of 335 patients with primary, secondary, and latent syphilis and symptomatic and asymptomatic neurosyphilis and of patients with certain neurological disorders. Of these, 230 (68·65%) patients had non-reactive results to this test. Of the remaining 105 patients, 78, 63, and 10 had reactive results with anti-IgG, IgM, and IgA conjugates respectively. Of the 129 cases of known syphilis, 11 were diagnosed as primary, 32 as secondary, and 50 as latent, and 36 patients had neurosyphilis. None of the specimens from the patients with primary syphilis gave reactive results to the test. Specimens from 21 (65·62%) of the 32 patients with secondary syphilis, 30 (60%) of the 50 patients with latent syphilis, and all (97·22%), except one, of the 36 patients with neurosyphilis gave reactive results to one at least of the IgG, IgM, or IgA FTA-CSF tests. Among the specimens from patients with secondary syphilis twice as many gave reactive results with anti-IgG conjugate than with anti-IgM conjugate. However, with specimens from patients with latent syphilis and neurosyphilis this ratio was diminished to 1·5:1. The Kolmer complement-fixation test, although superior in sensitivity and specificity to the Venereal Disease Research Laboratory (VDRL) test, in patients with secondary and latent syphilis and neurosyphilis, was greatly inferior to the FTA-CSF test. Data indicate that anti-treponemal antibodies can be detected in the spinal fluid even in patients with no neurological symptoms in cases of secondary syphilis and that the FTA-CSF test can be a valuable tool in the early detection of an immunological response to treponemal infection in the spinal fluid.
机译:使用单特异性结合物抗IgG,IgM和IgA对脑脊液(FTA-CSF)进行荧光性端螺旋体抗体测试,以确定335例原发性,继发性和潜伏性梅毒患者的脊髓液中是否存在抗链蛋白抗体。和有症状和无症状的神经梅毒以及某些神经系统疾病的患者。在这些患者中,有230位(68·65%)患者对此测试无反应。在其余的105位患者中,分别有78、63和10位患者分别与抗IgG,IgM和IgA缀合物反应。在129例梅毒中,诊断为原发性11例,继发性32例,潜伏50例,神经梅毒36例。原发性梅毒患者的标本均未对试验产生反应结果。 32例继发性梅毒患者中有21例(65·62%),50例潜在梅毒患者中有30例(60%)以及36例神经梅毒患者中除1例以外的所有(97·22%)至少对IgG,IgM或IgA FTA-CSF测试中的一项进行检测。在继发性梅毒患者的标本中,抗-IgG缀合物的反应结果是抗-IgM缀合物的两倍。但是,对于来自潜在梅毒和神经梅毒患者的标本,该比例降低到1·5:1。在继发性和潜伏性梅毒和神经性梅毒患者中,Kolmer补体固定试验虽然在敏感性和特异性方面优于性病研究实验室(VDRL),但远不及FTA-CSF试验。数据表明,即使在继发性梅毒病例中没有神经系统症状的患者中,也可以在脊髓液中检测到抗螺旋体抗体,并且FTA-CSF测试可以作为早期检测对甲状旁腺病毒感染的免疫反应的有价值的工具。脊髓液。

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