人疱疹病毒8免疫原糖蛋白K8.1单克隆抗体的制备。

Hybridoma Pub Date : 2000-08-01 DOI:10.1089/027245700429837
D Lang, A Birkmann, F Neipel, W Hinderer, M Rothe, M Ernst, H H Sonneborn
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引用次数: 6

摘要

人类疱疹病毒8 (HHV-8)与卡波西肉瘤(KS)、体腔淋巴瘤(BCBL)和某些形式的多灶性Castleman病(MCD)明显相关。它似乎是参与艾滋病相关KS发展的性传播媒介。HHV-8基因组总是存在于bcl衍生的细胞系中,在这些细胞系中,可以用磷酸酯(PE)诱导病毒的裂解复制。第一代HHV-8血清学检测是基于这些细胞系。最近,已经确定了几个编码HHV-8抗原的基因。其中反应性最强的抗原是由HHV-8开放阅读框K8.1编码的。虽然K8.1没有表现出与任何其他已知基因的明显序列同源性,但它可能类似于Epstein-Barr的gp220/350或小鼠疱疹病毒-68的gp150,参与靶细胞识别的病毒粒子-包膜糖蛋白。用纯化的大肠杆菌表达的GST-K8.1融合蛋白免疫小鼠。小鼠浆细胞与骨髓瘤细胞系P3-X63-Ag8融合后。制备了特异性针对K8.1蛋白的单克隆抗体(mab)。利用重组GST-K8.1突变体和k8.1特异性肽,通过缺失突变体分析确定每个单抗的结合位点。这些单克隆抗体识别的表位无一例外地位于蛋白的n端[氨基酸(aa) 29 ~ 80],从而鉴定出一个高度免疫原性的区域。这些抗体不仅是诊断HHV-8的有用工具,而且有助于分析K8.1的功能。
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Generation of monoclonal antibodies directed against the immunogenic glycoprotein K8.1 of human herpesvirus 8.

Human Herpesvirus 8 (HHV-8) is clearly associated with Kaposi's sarcoma (KS), body cavity-based lymphomas (BCBL), and certain forms of multifocal Castleman's disease (MCD). It appears to be the sexually transmissible agent involved in the development of AIDS-associated KS. HHV-8 genomes are invariably present in BCBL-derived cell lines where lytic replication of the virus can be induced by phorbol esters (PE). First-generation HHV-8 serological assays were based on these cell lines. More recently, several genes encoding HHV-8 antigens have been identified. One of the most reactive antigens is encoded by HHV-8 open reading frame K8.1. Although K8.1 does not exhibit overt sequence homology to any other known gene, it is likely to be analogous to gp220/350 of Epstein-Barr or gp150 of murine herpesvirus-68, virion-envelope glycoproteins involved in target cell recognition. Mice were immunized with purified GST-K8.1 fusion protein expressed in E. coli. After fusion of murine plasma cells with the myeloma cell line P3-X63-Ag8. monoclonal antibodies (MAbs) were generated, which are specifically directed against K8.1 protein. The binding site for each MAb was identified by deletion mutant analysis using recombinant GST-K8.1 mutants and K8.1-specific peptides. Without exception, the epitopes recognized by these MAbs were located within the N-terminal part of the protein [amino acids (aa) 29 to 80], thus identifying a highly immunogenic region. These antibodies will not only be useful tools for HHV-8 diagnostics, but will also facilitate the analysis of K8.1 function.

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来源期刊
Hybridoma
Hybridoma 医学-免疫学
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4-8 weeks
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