Chugai Pharmaceutical Co. Ltd., Fuji-Gotemba Research Laboratories, Shizuoka, Japan.
MAbs. 2011 May-Jun;3(3):243-52. doi: 10.4161/mabs.3.3.15234. Epub 2011 May 1.
Since the first generation of humanized IgG1 antibodies reached the market in the late 1990s, IgG antibody molecules have been extensively engineered. The success of antibody therapeutics has introduced severe competition in developing novel therapeutic monoclonal antibodies, especially for promising or clinically validated targets. Such competition has led researchers to generate so-called second or third generation antibodies with clinical differentiation utilizing various engineering and optimization technologies. Parent IgG antibodies can be engineered to have improved antigen binding properties, effector functions, pharmacokinetics, pharmaceutical properties and safety issues. Although the primary role of the antibody variable region is to bind to the antigen, it is also the main source of antibody diversity and its sequence affects various properties important for developing antibody therapeutics. Here we review recent research activity in variable region engineering to generate superior antibody therapeutics.
自 20 世纪 90 年代末第一代人源化 IgG1 抗体进入市场以来,IgG 抗体分子已得到广泛的工程改造。抗体治疗药物的成功带来了开发新型治疗性单克隆抗体的激烈竞争,尤其是针对有前景或经临床验证的靶点。这种竞争促使研究人员利用各种工程和优化技术,产生具有临床差异化的所谓第二代或第三代抗体。亲本 IgG 抗体可以被工程改造以提高抗原结合特性、效应功能、药代动力学、药物性质和安全性问题。尽管抗体可变区的主要作用是与抗原结合,但它也是抗体多样性的主要来源,其序列影响开发抗体治疗药物的各种重要特性。在这里,我们回顾了可变区工程改造的最新研究进展,以生成更优秀的抗体治疗药物。