Epiphany Biosciences Inc., San Francisco, CA 94111, USA.
J Hepatol. 2009 Nov;51(5):939-48. doi: 10.1016/j.jhep.2009.08.004. Epub 2009 Sep 10.
This review describes work conducted largely in my laboratory at the Chiron Corporation between 1982 and 1989 that led to the identification of the hepatitis C virus (HCV). Key colleagues included Dr. Qui-Lim Choo in my laboratory and Dr. George Kuo also of Chiron as well as my collaborator Dr. Daniel Bradley at the CDC who provided many biological samples from the NANBH chimpanzee model. Numerous molecular approaches were explored including the screening of tens of millions of bacterial cDNA clones derived from these materials. While this early genomics approach resulted in the identification of many host gene activities associated with NANBH, no genes of proven infectious etiology could be identified. A separate avenue of our research led to the molecular characterization of the complete hepatitis delta viral genome but unfortunately, this could not be used as a molecular handle for HCV. Largely following input from Dr. Kuo, I initiated a blind cDNA immunoscreening approach involving the large-scale screening of bacterial proteomic cDNA libraries derived from NANBH-infectious chimpanzee materials (prior to the development of PCR technology) using sera from NANBH patients as a presumptive source of viral antibodies. Eventually, this novel approach to identifying agents of infectious etiology led to the isolation of a single small cDNA clone that was proven to be derived from the HCV genome using various molecular and serological criteria. This discovery has facilitated the development of effective diagnostics, blood screening tests and the elucidation of promising drug and vaccine targets to control this global pathogen.
这篇综述描述了我在 Chiron 公司实验室于 1982 年至 1989 年期间进行的大部分工作,这些工作导致了丙型肝炎病毒(HCV)的鉴定。关键的同事包括我实验室的 Qui-Lim Choo 博士和 Chiron 的 George Kuo 博士,以及我在 CDC 的合作者 Daniel Bradley 博士,他提供了许多来自 NANBH 黑猩猩模型的生物样本。我们探索了许多分子方法,包括对源自这些材料的数千万个细菌 cDNA 克隆进行筛选。虽然这种早期的基因组学方法导致了与 NANBH 相关的许多宿主基因活动的鉴定,但无法鉴定出具有明确传染性病因的基因。我们研究的另一个途径导致了完整的乙型肝炎 delta 病毒基因组的分子特征描述,但不幸的是,这不能用作 HCV 的分子处理。在很大程度上是由于 Kuo 博士的建议,我开始采用一种盲目的 cDNA 免疫筛选方法,涉及使用 NANBH 患者的血清作为病毒抗体的假定来源,对源自 NANBH 感染的黑猩猩材料的大规模细菌蛋白质组 cDNA 文库进行筛选(在 PCR 技术发展之前)。最终,这种鉴定传染性病因因子的新方法导致了单个小 cDNA 克隆的分离,该克隆使用各种分子和血清学标准被证明源自 HCV 基因组。这一发现促进了有效的诊断、血液筛查测试的发展,并阐明了有前途的药物和疫苗靶点,以控制这种全球病原体。