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首页> 外文期刊>Journal of Clinical Microbiology >Immunodetection of human T-cell lymphotropic virus type I core protein in biological samples by using a monoclonal antibody immunoassay.
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Immunodetection of human T-cell lymphotropic virus type I core protein in biological samples by using a monoclonal antibody immunoassay.

机译:通过使用单克隆抗体免疫测定法对生物样品中的人T细胞淋巴病毒I型核心蛋白进行免疫检测。

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摘要

A monoclonal antibody-based enzyme immunoassay (EIA) has been developed for detection of human T-cell lymphotropic virus type I (HTLV-I) core protein. The monoclonal antibody (clone 6.11) specifically recognizes the p19 gag gene-encoded protein of the virus. The EIA was over 100 times more sensitive than reverse transcriptase measurement and was capable of responding to less than 500 pg of whole-virus lysate. The assay exhibited type specificity in that HTLV-II antigens failed to produce a positive signal. In addition, a panel of other viruses demonstrated no antigenic cross-reactivity. These included herpesviruses, measles virus, human immunodeficiency viruses, and others. Viral p19 was followed during the course of density gradient ultracentrifugation in the presence of detergent, where it was noted to associate with viral membrane proteins. In comparison, reverse transcriptase activity localized in fractions of higher density containing envelope-free cores. Of clinical interest, the EIA was used to detect HTLV-I antigen in the viral cultures of patients with HTLV-I-associated myelopathies and from symptom-free individuals with proviral integration.
机译:已经开发了一种基于单克隆抗体的酶免疫测定(EIA),用于检测人T细胞I型淋巴病毒(HTLV-1)核心蛋白。单克隆抗体(克隆6.11)特异性识别病毒的p19 gag基因编码蛋白。 EIA的灵敏度比逆转录酶测量的灵敏度高100倍以上,并且能够响应小于500 pg的全病毒裂解液。该测定法表现出类型特异性,因为HTLV-II抗原未能产生阳性信号。另外,一组其他病毒没有显示出抗原交叉反应性。这些病毒包括疱疹病毒,麻疹病毒,人类免疫缺陷病毒等。在去污剂存在下,在密度梯度超速离心过程中跟踪病毒p19,在那里它与病毒膜蛋白有关。相比之下,逆转录酶活性位于包含无包膜核心的较高密度级分中。具有临床意义的EIA用于检测HTLV-I相关性骨髓病患者和无症状个体的病毒培养物中的HTLV-I抗原。

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