Oliveira Heliana B, Machado Gleyce A, Mineo José R, Costa-Cruz Julia M
Departamento de Imunologia, Microbiologia e Parasitologia, Instituto de Ciências Biomédicas, Universidade Federal de Uberlândia, 38400-902 Uberlândia, Minas Gerais, Brazil.
Clin Vaccine Immunol. 2010 Apr;17(4):638-44. doi: 10.1128/CVI.00516-09. Epub 2010 Feb 3.
Taenia saginata metacestode antigens have been constituted a useful alternative antigen for neurocysticercosis (NC) serodiagnosis, particularly due to an increasing difficulty to obtain Taenia solium homologous antigen. Cross-reactivity with Echinococcus granulosus infection occurs in homologous and heterologous antigens and could be avoided by using different purified methods. The present study evaluated antigen fractions obtained from saline extracts of T. saginata metacestodes purified by affinity chromatography with jacalin or concanavalin A (ConA) lectins to detect IgG antibodies by enzyme-linked immunosorbent assay (ELISA) and immunoblot analysis to diagnose human NC. Serum samples were collected from 142 individuals: 40 of them were diagnosed with NC, 62 presented Taenia sp. and other parasites, and 40 were apparently healthy individuals. The jacalin- and ConA-unbound fractions demonstrated sensitivity and specificity higher than those of bound fractions. Among unbound fractions, ConA demonstrated statistically higher sensitivity and specificity by ELISA (90% and 93.1%, respectively). By immunoblot assay, the 64- to 68-kDa component from the ConA-unbound fraction showed 100% sensitivity and specificity, making this component suitable for use as a specific antigen for diagnosis of NC. To our knowledge, this is the first report showing the relevance of using the unbound ConA fraction of T. saginata metacestodes to diagnose NC. In conclusion, the results obtained herein clearly demonstrate that antigenic fractions without affinity to ConA, obtained from T. saginata metacestodes, are an important source of specific peptides and are efficient in the diagnosis of NC when tested by immunoblot assay.
牛带绦虫囊尾蚴抗原已成为神经囊尾蚴病(NC)血清学诊断的一种有用的替代抗原,特别是由于获得猪带绦虫同源抗原的难度日益增加。与细粒棘球绦虫感染的交叉反应在同源和异源抗原中均会发生,可通过使用不同的纯化方法来避免。本研究评估了通过与红豆蔻凝集素或伴刀豆球蛋白A(ConA)凝集素进行亲和层析纯化从牛带绦虫囊尾蚴的盐水提取物中获得的抗原组分,以通过酶联免疫吸附测定(ELISA)和免疫印迹分析来检测IgG抗体,从而诊断人类NC。从142名个体中采集血清样本:其中40人被诊断为NC,62人感染了带绦虫属和其他寄生虫,40人为明显健康个体。红豆蔻凝集素和ConA未结合组分显示出比结合组分更高的敏感性和特异性。在未结合组分中,ConA通过ELISA显示出统计学上更高的敏感性和特异性(分别为90%和93.1%)。通过免疫印迹测定,ConA未结合组分中的64至68 kDa成分显示出100%的敏感性和特异性,使得该成分适合用作诊断NC的特异性抗原。据我们所知,这是第一份显示使用牛带绦虫囊尾蚴的未结合ConA组分诊断NC的相关性的报告。总之,本文获得的结果清楚地表明,从牛带绦虫囊尾蚴获得的与ConA无亲和力的抗原组分是特异性肽的重要来源,并且通过免疫印迹测定进行检测时在NC诊断中是有效的。