Lonberg Nils
Medarex, 521 Cottonwood Drive, Milpitas, California 95035, USA.
Nat Biotechnol. 2005 Sep;23(9):1117-25. doi: 10.1038/nbt1135.
Laboratory mice provide a ready source of diverse, high-affinity and high-specificity monoclonal antibodies (mAbs). However, development of rodent antibodies as therapeutic agents has been impaired by the inherent immunogenicity of these molecules. One technology that has been explored to generate low immunogenicity mAbs for in vivo therapy involves the use of transgenic mice expressing repertoires of human antibody gene sequences. This technology has now been exploited by over a dozen different pharmaceutical and biotechnology companies toward developing new therapeutic mAbs, and currently at least 33 different drugs in clinical testing--including several in pivotal trials--contain variable regions encoded by human sequences from transgenic mice. The emerging data from these trials provide an early glimpse of the safety and efficacy issues for these molecules. Nevertheless, actual product approval, the biggest challenge so far, is required to fully validate this technology as a drug discovery tool. In the future, it may be possible to extend this technology beyond rodents and use transgenic farm animals to directly generate and produce human sequence polyclonal sera.
实验室小鼠可提供来源丰富、具有高亲和力和高特异性的单克隆抗体(mAb)。然而,由于这些分子固有的免疫原性,啮齿动物抗体作为治疗剂的开发受到了阻碍。为生成用于体内治疗的低免疫原性单克隆抗体而探索的一项技术,涉及使用表达人抗体基因序列库的转基因小鼠。目前已有十几家不同的制药和生物技术公司利用这项技术来开发新的治疗性单克隆抗体,目前至少有33种不同的药物正在进行临床试验——包括几种关键试验药物——含有来自转基因小鼠的人序列编码的可变区。这些试验中出现的数据让我们初步了解了这些分子的安全性和有效性问题。然而,要充分验证这项技术作为药物发现工具的有效性,还需要实际获得产品批准,这是迄今为止最大的挑战。未来,有可能将这项技术扩展到啮齿动物之外,利用转基因农场动物直接生成并生产人序列多克隆血清。