双特异性抗体
抗体
免疫球蛋白轻链
重链
计算生物学
碎片结晶区
计算机科学
免疫学
生物
单克隆抗体
作者
Christian Klein,Wolfgang Schäfer,Jörg T. Regula
出处
期刊:mAbs
[Landes Bioscience]
日期:2016-06-10
卷期号:8 (6): 1010-1020
被引量:185
标识
DOI:10.1080/19420862.2016.1197457
摘要
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.
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