Method of using a bispecific antibody to conditionally inhibit a receptor signaling complex
AssigneeTorch Therapeutics
InventorsTodd M. Kinsella, Donald G. Payan, Ramesh Bhatt, Kristen Baltgalvis
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Abstract
This invention describes the design of bispecific antibodies that function as conditionally effective therapeutics by binding to a functionally silent epitope on one component of a targeted signaling complex and simultaneously binding to a second protein, whose expression or accessibility is cell- or disease environment-specific, and whose antibody-driven proximity to the signaling complex leads to an alteration of signal transduction.
Claims1
A method of conditionally inhibiting a receptor signaling complex (RSC) comprising a receptor protein and a receptor ligand in a target cell comprising:
- a) providing a cell capable of forming said receptor signaling complex, wherein said receptor protein binds said ligand at an active site;
- b) contacting said cell with a bispecific antibody comprising:
- i) a first antigen binding domain that binds to said receptor protein at a first epitope outside of said active site;
- ii) a second antigen binding domain that binds to a target protein;
- c) wherein if said cell expresses said target protein, said first antigen binding domain binds to said receptor protein and said second antigen binding domain binds to said target protein, thereby inhibiting the binding of said receptor protein and said ligand to reduce signaling;
- and
- d) wherein if said cell does not express said target protein, said first antigen binding domain binds to said receptor protein and does not prevent binding of said ligand to said receptor protein to achieve receptor signaling, and
- e) and wherein said receptor protein/target protein pair is selected from the group consisting of Type II Receptor for TGFβ (TGFBR2)/CD45, TGFBR2/Fibroblast Activation Protein (FAP), TGFBR2/Beta-3 Adrenergic Receptor (ADRB3), Colony Stimulating Factor 2 Receptor Alpha Subunit (GMCSFRα)/CD33, Signal-Regulatory Protein Alpha (SIRPα)/Programmed death-ligand 1 (PD-L1), Interleukin 2 Receptor (IL2R)/Layilin (LAYN), Program cell death protein 1 (PD-1)/Potassium Calcium-Activated Channel Subfamily M Alpha 1 (KCNMA1) and Glycoprotein 130 (gp130)/PD-L1.
Dependencies are inferred from the claim text.