Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
Protein Cell. 2010 Apr;1(4):319-330. doi: 10.1007/s13238-010-0052-8. Epub 2010 May 8.
The study of antibodies has been a focal point in modern biology and medicine since the early 1900s. However, progress in therapeutic antibody development was slow and intermittent until recently. The first antibody therapy, murine-derived murononab OKT3 for acute organ rejection, was approved by the US Food and Drug Administration (FDA) in 1986, more than a decade after César Milstein and Georges Köhler developed methods for the isolation of mouse monoclonal antibodies from hybridoma cells in 1975. As a result of the scientific, technological, and clinical breakthroughs in the 1980s and 1990s, the pace of therapeutic antibody discovery and development accelerated. Antibodies are becoming a major drug modality with more than two dozen therapeutic antibodies in the clinic and hundreds more in development. Despite the progress, need for improvement exists at every level. Antibody therapeutics provides fertile ground for protein scientists to fulfill the dream of personalized medicine through basic scientific discovery and technological innovation.
自 20 世纪初以来,抗体的研究一直是现代生物学和医学的重点。然而,直到最近,治疗性抗体的发展才缓慢而间歇性地取得进展。第一种抗体疗法,即用于急性器官排斥的鼠源性 murononab OKT3,于 1986 年获得美国食品和药物管理局(FDA)批准,而 César Milstein 和 Georges Köhler 于 1975 年开发出从杂交瘤细胞中分离小鼠单克隆抗体的方法,这一方法的出现比这一事件晚了十多年。由于 20 世纪 80 年代和 90 年代的科学、技术和临床突破,治疗性抗体的发现和开发速度加快。抗体正在成为一种主要的药物模式,有二十多种治疗性抗体在临床上使用,还有数百种正在开发中。尽管取得了进展,但在各个层面都需要改进。抗体疗法为蛋白质科学家提供了肥沃的土壤,通过基础科学发现和技术创新实现个性化医疗的梦想。