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首页> 外文期刊>Journal of Clinical Microbiology >Cysticercosis Immunodiagnosis Using 18- and 14-Kilodalton Proteins from Taenia crassiceps Cysticercus Antigens Obtained by Immunoaffinity Chromatography
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Cysticercosis Immunodiagnosis Using 18- and 14-Kilodalton Proteins from Taenia crassiceps Cysticercus Antigens Obtained by Immunoaffinity Chromatography

机译:使用免疫亲和色谱法从Ta虫(Taenia crassiceps)的囊性囊尾Cy抗原(Sticticercus Antigens)获得的18和14-Kilodalton蛋白对囊尾osis的免疫诊断

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摘要

Monoclonal antibodies (MAb) against Taenia crassiceps and Taenia solium cysticerci were produced and showed cross-reactivity with a 14-kDa protein from T. solium and with 18- and 14-kDa proteins from T. crassiceps. These MAbs and antibodies from cerebrospinal fluid (CSF) as well as serum samples from patients with neurocysticercosis (NC) reacted with 18- and 14-kDa T. crassiceps proteins purified by immunoaffinity chromatography using a Sepharose column coupled with MAbs (anti-excretory/secretory or anti-vesicular fluid antigens). Immunoaffinity-purified 18- and 14-kDa proteins were used in the design of a diagnostic enzyme-linked immunosorbent assay (ELISA) to detect antibodies in 23 CSF and 20 serum samples from patients with NC, showing 100% sensitivity. The test specificity was determined using 42 noninflammatory CSF samples and 70 inflammatory CSF samples from patients with other neurological disorders (OND), showing 100% and 99.1% (confidence interval, 97.3% to 100%) specificity, respectively. A false-positive CSF sample result in the OND group was from a human immunodeficiency virus-positive patient with meningoencephalitis. By using serum samples from 194 healthy individuals, the specificity was 100%. Analysis of an additional 16 serum samples from individuals with other parasitic diseases (13 with intestinal parasitosis and 3 with schistosomiasis) showed negative results. Three (10%) serum samples from patients with hydatidosis were positive in our ELISA and in ELISA with T. solium cysticerci antigens. Two of them were also positive by immunoblotting. The use of 18- and 14-kDa T. crassiceps immunoaffinity-purified proteins for detection of anti-cysticercus antibodies in CSF and/or serum samples using an ELISA system showed a good performance and high specificity for serum samples, dispensing with the use of confirmatory tests, such as immunoblotting, for checking specificity.
机译:产生了针对 Taenia crassiceps Taenia solium cysticerci的单克隆抗体(MAb),并显示了与 T的14 kDa蛋白的交叉反应性。 以及来自 T的18-kDa和14-kDa蛋白。狂犬病。这些来自脑脊液(CSF)的MAb和抗体以及患有神经囊虫病(NC)的患者的血清样品与18-kDa和14-kDa Tem反应。用琼脂糖凝胶柱和单克隆抗体(抗排泄/分泌或抗水泡液抗原)通过免疫亲和层析纯化的猪ass虫蛋白质。免疫亲和纯化的18kDa和14kDa蛋白用于诊断性酶联免疫吸附测定(ELISA)设计,以检测23例CSF和20例NC患者的血清样品中的抗体,显示出100%的敏感性。使用来自其他神经系统疾病(OND)患者的42份非炎性CSF样品和70份炎性CSF样品确定测试特异性,分别显示100%和99.1%(置信区间97.3%至100%)。 OND组的CSF假阳性结果来自一名患有脑膜脑炎的人类免疫缺陷病毒阳性患者。通过使用来自194名健康个体的血清样本,特异性为100%。从其他寄生虫病患者中另外采集了16个血清样本(13例是肠道寄生虫病,而3例是血吸虫病),结果显示阴性。在我们的ELISA和 T ELISA中,有3例(10%)葡萄胎患者的血清样品呈阳性。猪囊尾er抗原。其中两个通过免疫印迹也呈阳性。 18 kDa和14 kDa T的使用。使用ELISA系统检测猪笼草的Caf和/或血清样品中抗半胱氨酸抗体的亲和力纯化蛋白,对血清样品表现出良好的性能和高特异性,并且无需使用诸如免疫印迹,用于检查特异性。

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