人乳头瘤病毒E6和E7癌蛋白单克隆抗体的制备和鉴定。

A. Wlazlo, W. Giles-Davis, A. Clements, G. Struble, R. Marmorstein, H. Ertl
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引用次数: 5

摘要

三种针对人乳头瘤病毒(HPV)主要癌蛋白的单克隆抗体(mab)的产生是通过高强度的初始/增强方案完成的。用表达HPV-16的E6或E7癌蛋白的表达载体转染小鼠,然后用牛痘病毒构建体和复制缺陷的人株5缺失腺病毒重组体增强,最后用杆状病毒衍生的HPV-16 E6和E7蛋白在不完全Freunds佐剂中增强。然后将脾细胞与骨髓瘤细胞系融合。接种方案产生1个IgM亚型的抗e7单抗和2个IgG1亚型的抗e6单抗。在标准的实验室检测中测试了单克隆抗体的功能,发现它们分别检测E6和E7蛋白。E7单抗与HPV-1a E7癌蛋白发生交叉反应。单克隆抗体的结合位点被映射到每个病毒蛋白的定义区域。
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Generation and characterization of monoclonal antibodies against the E6 and E7 oncoproteins of HPV.
Generation of three monoclonal antibodies (MAbs) to the major oncoproteins of human papillomavirus (HPV) was accomplished by an intense prime/boost regimen. Mice were primed with expression vectors expressing either the E6 or E7 oncoproteins of HPV-16 followed by boosting with a vaccinia virus construct and a replication-defective E1-deleted adenoviral recombinant of the human strain 5, and last, with baculovirus-derived HPV-16 E6 and E7 proteins in incomplete Freunds' adjuvant. Splenocytes were then fused with a myeloma cell line. The vaccination protocol generated one anti-E7 MAb of the IgM isotype and two anti-E6 MAbs of the IgG1 subisotype. The MAbs were tested for functionality in standard laboratory assays and found to detect the E6 and E7 proteins, respectively. The E7 MAb cross-reacted with the HPV-1a E7 oncoprotein. The binding sites of the MAbs were mapped to defined regions of each viral protein.
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来源期刊
Hybridoma
Hybridoma 医学-免疫学
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审稿时长
4-8 weeks
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