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用于诊断肠道病毒71型的单克隆抗体。

Monoclonal antibodies for diagnosis of enterovirus 71.

作者信息

Xu Li, Huang Kao-Jean, Ho Tzong-Shiann, Liu Chia-Chyi, Lee Ying-Ray, Lin Ching-Yen, Shiuan David, Jiang Xing-Hong

机构信息

1 Key Laboratory of Pain Basic Research and Clinical Therapy, Department of Neurobiology, Medical College of Soochow University , Suzhou, China .

出版信息

Monoclon Antib Immunodiagn Immunother. 2013 Dec;32(6):386-94. doi: 10.1089/mab.2013.0033.

Abstract

Enterovirus 71 (EV71), one of the major causative agents of hand, foot, and mouth disease (HFMD), is now recognized as an emerging neurotropic virus in Asia and may cause severe neurologic complications and mortalities. Laboratory diagnosis of EV71 infection must be efficient and accurate, which could be accomplished by various immunoassays. In this study we use a live EV71 isolate, Tainan/4643/98, with genotype C2 as an immunogen to sensitize BALB/c (H-2(d)) mice and then generate the EV71-specific murine monoclonal antibodies. Five hybridoma clones were established and their monoclonal antibodies were characterized. All five clones are applicable in immunofluorescence staining but with different sensitivities-that is, MAbs 22, 24, and 27 were sensitive in IFA detection, and MAbs 22 and 24 were also confirmed in flow cytometry. None of these cross-reacted with coxsackievirus A16 (CVA16) or Echovirus type 6 (ECHO6), but each varied in binding to different EV71 subgenogroups (B1, B4, B5, C2, and C4). Western blot analysis revealed that all of these MAbs reacted with EV71 VP1 capsid proteins, and in addition MAbs 22 and 24 exhibited potent neutralizing activities against EV71 and protected cells from infection. Further, mapping the epitopes for each MAb revealed that only MAb 27 showed positive for the linear epitope DVIESSIGDSVSRAL, which was located at the N-terminus (a.a. 6-20) of EV71 VP1 and highly conserved among all EV71 subgenotypes. Thus, these MAbs may provide valuable tools for the laboratory diagnosis of EV71 infection and for vaccine development.

摘要

肠道病毒71型(EV71)是手足口病(HFMD)的主要病原体之一,目前在亚洲被认为是一种新出现的嗜神经病毒,可导致严重的神经系统并发症和死亡。EV71感染的实验室诊断必须高效且准确,这可通过各种免疫测定来实现。在本研究中,我们使用一株活的EV71分离株,台南/4643/98,其基因型为C2,作为免疫原致敏BALB/c(H-2(d))小鼠,然后产生EV71特异性鼠单克隆抗体。建立了五个杂交瘤克隆并对其单克隆抗体进行了表征。所有五个克隆都适用于免疫荧光染色,但灵敏度不同——即单克隆抗体22、24和27在免疫荧光分析检测中敏感,单克隆抗体22和24在流式细胞术中也得到证实。这些单克隆抗体均不与柯萨奇病毒A16型(CVA16)或埃可病毒6型(ECHO6)发生交叉反应,但在与不同的EV71亚基因群(B1、B4、B5、C2和C4)结合方面存在差异。蛋白质印迹分析表明,所有这些单克隆抗体均与EV71 VP1衣壳蛋白发生反应,此外,单克隆抗体22和24对EV71表现出强大的中和活性并保护细胞免受感染。此外,对每个单克隆抗体的表位进行定位显示,只有单克隆抗体27对线性表位DVIESSIGDSVSRAL呈阳性,该表位位于EV71 VP蛋白的N端(第6至20位氨基酸),在所有EV71亚型中高度保守。因此,这些单克隆抗体可为EV71感染的实验室诊断和疫苗开发提供有价值的工具。

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