The Jake Gittlen Cancer Research Foundation and Department of Pathology, Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.
J Gen Virol. 2010 Jul;91(Pt 7):1834-9. doi: 10.1099/vir.0.017228-0. Epub 2010 Feb 24.
Human papillomavirus (HPV) 58 is a high-risk HPV type associated with progression to invasive genital carcinomas. We developed six monoclonal antibodies (mAbs) against HPV58 L1 virus-like particles that bind conformational epitopes on HPV58. The hybridoma cell lines were adapted to serum- and animal component-free conditions and the mAb supernatants were affinity-purified. The six mAbs neutralized HPV58 pseudoviruses (PsVs) and 'quasivirions' with different capacities. The mAbs differed in their ability to prevent PsV58 attachment to HaCaT cells, to the extracellular matrix (ECM) deposited by HaCaT cells, to heparin and to purified human laminin 5, a protein in the ECM. These mAbs provide a unique set of tools to study the binding properties of a previously untested, high-risk HPV type and the opportunity to compare these characteristics with the binding of other HPV types.
人乳头瘤病毒(HPV)58 是一种与侵袭性生殖器癌进展相关的高危 HPV 类型。我们开发了针对 HPV58 L1 病毒样颗粒的六种单克隆抗体(mAb),这些 mAb 可结合 HPV58 上的构象表位。杂交瘤细胞系适应于无血清和动物成分的条件,mAb 上清液经过亲和纯化。这六种 mAb 以不同的能力中和 HPV58 假病毒(PsV)和“准病毒”。mAb 在阻止 PsV58 附着到 HaCaT 细胞、附着到 HaCaT 细胞分泌的细胞外基质(ECM)、附着肝素和附着纯化的人层粘连蛋白 5(ECM 中的一种蛋白质)方面的能力有所不同。这些 mAb 提供了一组独特的工具,可用于研究以前未经测试的高危 HPV 类型的结合特性,并提供了与其他 HPV 类型的结合特性进行比较的机会。