Magnarelli L A, Anderson J F
Department of Entomology, Connecticut Agricultural Experiment Station, New Haven 06504.
J Clin Microbiol. 1991 Sep;29(9):1761-4. doi: 10.1128/jcm.29.9.1761-1764.1991.
Serum samples from persons with Lyme borreliosis, periodontitis, or acute necrotizing ulcerative gingivitis were analyzed by an enzyme-linked immunosorbent assay (ELISA) with and without adsorption and amplification procedures. When biotin and streptavidin reagents were used as an amplification procedure in ELISA without the use of commercially prepared sorbent (Treponema phagedenis biotype Reiter), sensitivity increased. Of the 85 serum samples collected from persons with erythema migrans but no detectable antibodies to Borrelia burgdorferi by standard ELISA, 17 (20%) were reactive after amplification. Adsorption of serum samples with a 1:10 dilution of T. phagedenis biotype Reiter sorbent used in conjunction with amplified ELISA also improved the sensitivity of this method. However, cross-reactivity could not be completely eliminated. An adsorbed-amplified ELISA may be helpful in the diagnosis of Lyme borreliosis in the laboratory, particularly during early weeks of infection, when antibodies to B. burgdorferi can be present at a low concentration.
采用酶联免疫吸附测定(ELISA),在有或无吸附及扩增程序的情况下,对莱姆病、牙周炎或急性坏死性溃疡性龈炎患者的血清样本进行了分析。在不使用商业制备吸附剂(噬菌体型赖特密螺旋体)的ELISA中,当使用生物素和链霉抗生物素蛋白试剂作为扩增程序时,灵敏度有所提高。在从患有游走性红斑但通过标准ELISA检测不到抗伯氏疏螺旋体抗体的患者中采集的85份血清样本中,17份(20%)在扩增后呈反应性。将噬菌体型赖特密螺旋体吸附剂以1:10稀释后对血清样本进行吸附,并与扩增后的ELISA联合使用,也提高了该方法的灵敏度。然而,交叉反应性无法完全消除。吸附 - 扩增ELISA在实验室诊断莱姆病中可能会有帮助,特别是在感染的早期几周,此时抗伯氏疏螺旋体抗体可能以低浓度存在。