双特异性抗体
抗体
免疫学
计算生物学
免疫系统
抗体反应
生物
癌症研究
单克隆抗体
作者
Feng Wang,Jordan C. Tsai,Jonathan H. Davis,Bryant Chau,Jia Dong,Sean M. West,Jason M. Hogan,Matthew L. Wheeler,Christine Bee,Winse Morishige,Thomas Cayton,Donata David-brown,Chengyue Zhang,Alexander Kozhich,Tim W. Sproul,Gavin Dollinger,Arvind Rajpal,Pavel Strop
出处
期刊:mAbs
[Landes Bioscience]
日期:2019-12-19
卷期号:12 (1): 1685350-1685350
被引量:29
标识
DOI:10.1080/19420862.2019.1685350
摘要
The development of antibody therapeutics relies on animal models that accurately recapitulate disease biology. Syngeneic mouse models are increasingly used with new molecules to capture the biology of complex cancers and disease states, and to provide insight into the role of the immune system. The establishment of syngeneic mouse models requires the ability to generate surrogate mouse counterparts to antibodies designed for humans. In the field of bispecific antibodies, there remains a dearth of technologies available to generate native IgG-like mouse bispecific antibodies. Thus, we engineered a simple co-expression system for one-step purification of intact mouse IgG1 and IgG2a bispecific antibodies from any antibody pair. We demonstrated proof of concept with CD3/CD20 bispecific antibodies, which highlighted both the quality and efficacy of materials generated by this technology.
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