Rapley R
School of Natural Sciences, Coventry University, Warwicks, UK.
Mol Biotechnol. 1995 Apr;3(2):139-54. doi: 10.1007/BF02789110.
The exquisite specificity of monoclonal antibodies (MAb) has long provided the potential for creating new reagents for the in vivo delivery of therapeutic drugs or toxins to defined cellular target sites or improved methods of diagnosis. However, many difficulties associated with their production, affinity, specificity, and use in vivo have largely confined their application to research or in vitro diagnostics. This situation is beginning to change with the recent developments in the applied molecular techniques that allow the engineering of the genes that encode antibodies rather than the manipulation of the intact antibodies themselves. Techniques, such as the polymerase chain reaction, have provided essential methods with which to generate and modify the genetic constituents of antibodies, allow their conjugation to toxins or drugs, provide ways of humanizing murine antibodies, and allow discrete modular antigen binding components to be produced. More recent developments of in vitro expression systems and powerful phage surface display technologies will without doubt play a major role in future antibody engineering and in the successful development of new diagnostic and therapeutic antibody-based reagents.
单克隆抗体(MAb)的高度特异性长期以来为研发新试剂提供了潜力,这些新试剂可用于将治疗药物或毒素体内递送至特定细胞靶点,或改进诊断方法。然而,与它们的生产、亲和力、特异性以及体内应用相关的许多困难,在很大程度上限制了它们仅应用于研究或体外诊断。随着应用分子技术的最新进展,这种情况开始发生变化,这些技术允许对编码抗体的基因进行工程改造,而不是直接操纵完整的抗体本身。诸如聚合酶链反应等技术,提供了生成和修饰抗体遗传成分的基本方法,使其能够与毒素或药物偶联,提供人源化鼠源抗体的方法,并允许生产离散的模块化抗原结合成分。体外表达系统和强大的噬菌体表面展示技术的最新进展,无疑将在未来的抗体工程以及基于抗体的新诊断和治疗试剂的成功开发中发挥重要作用。