Design and characterization of mouse IgG1 and IgG2a bispecific antibodies for use in syngeneic models

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...

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Main Authors: Feng Wang (Author), Jordan C. Tsai (Author), Jonathan H. Davis (Author), Bryant Chau (Author), Jia Dong (Author), Sean M. West (Author), Jason M. Hogan (Author), Matthew L. Wheeler (Author), Christine Bee (Author), Winse Morishige (Author), Thomas Cayton (Author), Donata David-brown (Author), Chengyue Zhang (Author), Alexander Kozhich (Author), Tim Sproul (Author), Gavin Dollinger (Author), Arvind Rajpal (Author), Pavel Strop (Author)
Format: Book
Published: Taylor & Francis Group, 2020-01-01T00:00:00Z.
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Summary: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.
Item Description:10.1080/19420862.2019.1685350
1942-0870
1942-0862