Klein Christian, Schaefer Wolfgang, Regula Jörg T
a Roche Innovation Center Zurich , Roche Pharmaceutical Research & Early Development, Wagistrasse , Schlieren , Switzerland.
b Roche Innovation Center Munich , Roche Pharmaceutical Research & Early Development, Nonnenwald , Penzberg , Germany.
MAbs. 2016 Aug-Sep;8(6):1010-20. doi: 10.1080/19420862.2016.1197457. Epub 2016 Jun 10.
The major challenge in the generation of bispecific IgG antibodies is enforcement of the correct heavy and light chain association. The correct association of generic light chains can be enabled using immunoglobulin domain crossover, known as CrossMAb technology, which can be combined with approaches enabling correct heavy chain association such as knobs-into-holes (KiH) technology or electrostatic steering. Since its development, this technology has proven to be very versatile, allowing the generation of various bispecific antibody formats, not only heterodimeric/asymmetric bivalent 1+1 CrossMAbs, but also tri- (2+1), tetravalent (2+2) bispecific and multispecific antibodies. Numerous CrossMAbs have been evaluated in preclinical studies, and, so far, 4 different tailor-made bispecific antibodies based on the CrossMAb technology have entered clinical studies. Here, we review the properties and activities of bispecific CrossMAbs and give an overview of the variety of CrossMAb-enabled antibody formats that differ from heterodimeric 1+1 bispecific IgG antibodies.
双特异性IgG抗体生成过程中的主要挑战在于确保重链和轻链的正确配对。利用免疫球蛋白结构域交叉技术(即CrossMAb技术)可实现通用轻链的正确配对,该技术可与能确保重链正确配对的方法(如“旋钮入孔”技术或静电引导)相结合。自该技术问世以来,已证明其具有很强的通用性,可生成各种双特异性抗体形式,不仅包括异源二聚体/不对称二价1+1 CrossMAb,还包括三价(2+1)、四价(2+2)双特异性和多特异性抗体。许多CrossMAb已在临床前研究中得到评估,迄今为止,已有4种基于CrossMAb技术的定制双特异性抗体进入临床研究。在此,我们综述双特异性CrossMAb的特性和活性,并概述与异源二聚体1+1双特异性IgG抗体不同的多种基于CrossMAb的抗体形式。