| Literature DB >> 32294319 |
Ling Huang1, Kalpana Shah1, Bhaswati Barat1, Chia-Ying K Lam2, Sergey Gorlatov1, Valentina Ciccarone1, James Tamura1, Paul A Moore1, Gundo Diedrich1.
Abstract
Multispecific antibodies bind two or more different antigens and enable new therapeutic applications that cannot be replicated with conventional monoclonal antibodies, such as bridging different cells or bringing soluble proteins in close proximity. The DART and TRIDENT platforms enable the engineering of such antibodies. A DART molecule combines two independent antigen-binding sites in a stabilized, diabody-like structure. A DART molecule can be expressed with or without an Fc domain and thus can be tailored to have a long or short half-life in vivo and to induce or ablate effector function. Linking two DART units or a DART unit and a Fab domain (the latter structure is called TRIDENT format) via an Fc domain creates a monospecific, bispecific, trispecific, or tetraspecific molecule with up to tetravalent targeting of antigens. This article focuses on the design of DART and TRIDENT molecules that target two or three different antigens.Entities:
Keywords: antibody; bispecific; diabody; trispecific; valency
Year: 2020 PMID: 32294319 DOI: 10.1002/cpim.95
Source DB: PubMed Journal: Curr Protoc Immunol ISSN: 1934-3671