| CPC C07K 16/40 (2013.01) [A61K 39/395 (2013.01); C07K 14/70575 (2013.01); C07K 14/70596 (2013.01); C07K 16/2803 (2013.01); C07K 16/2815 (2013.01); C07K 16/2896 (2013.01); C07K 16/3007 (2013.01); A61K 38/00 (2013.01); C07K 2317/33 (2013.01); C07K 2317/35 (2013.01); C07K 2317/522 (2013.01); C07K 2317/524 (2013.01); C07K 2317/526 (2013.01); C07K 2317/565 (2013.01); C07K 2317/60 (2013.01); C07K 2317/92 (2013.01); C07K 2319/30 (2013.01); C07K 2319/33 (2013.01)] | 28 Claims |
|
1. A method of treating cancer in an individual, comprising administering to said individual a therapeutically effective amount of a composition comprising a tumor necrosis factor (TNF) family ligand trimer-containing antigen-binding molecule in a pharmaceutically acceptable form, wherein the TNF family ligand trimer-containing antigen-binding molecule comprises:
(a) at least one antigen-binding domain comprising an antibody light chain variable region (VL) and an antibody heavy chain variable region (VH) capable of specific binding to a target cell antigen, wherein the target cell antigen is CD19, and
(b) a first polypeptide and a second polypeptide that are linked to each other by a disulfide bond, wherein the first polypeptide comprises two ectodomains of a TNF family ligand or fragments thereof that are connected to each other by a peptide linker and the second polypeptide comprises only one ectodomain of the TNF family ligand or fragment thereof,
wherein the TNF family ligand is 4-1BBL.
|