| Literature DB >> 23880771 |
Christoph Spiess1, Jack Bevers, Janet Jackman, Nancy Chiang, Gerald Nakamura, Michael Dillon, Hongbin Liu, Patricia Molina, J Michael Elliott, Whitney Shatz, Justin M Scheer, Glen Giese, Josefine Persson, Yin Zhang, Mark S Dennis, James Giulianotti, Prateek Gupta, Dorothea Reilly, Enzo Palma, Jianyong Wang, Eric Stefanich, Heleen Scheerens, Germaine Fuh, Lawren C Wu.
Abstract
Human bispecific antibodies have great potential for the treatment of human diseases. Although human IgG1 bispecific antibodies have been generated, few attempts have been reported in the scientific literature that extend bispecific antibodies to other human antibody isotypes. In this paper, we report our work expanding the knobs-into-holes bispecific antibody technology to the human IgG4 isotype. We apply this approach to generate a bispecific antibody that targets IL-4 and IL-13, two cytokines that play roles in type 2 inflammation. We show that IgG4 bispecific antibodies can be generated in large quantities with equivalent efficiency and quality and have comparable pharmacokinetic properties and lung partitioning, compared with the IgG1 isotype. This work broadens the range of published therapeutic bispecific antibodies with natural surface architecture and provides additional options for the generation of bispecific antibodies with differing effector functions through the use of different antibody isotypes.Entities:
Keywords: Antibody Engineering; Asthma; Cytokine; Immunoglobulin; Knobs-into-holes; Lebrikizumab; Lung; Protein Assembly
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Year: 2013 PMID: 23880771 PMCID: PMC3772205 DOI: 10.1074/jbc.M113.480483
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157