Methods for treating TWEAK-related conditions
View Patent ↗The present invention provides methods and agents for the treatment of TWEAK-related conditions, including cardiac, liver, kidney, lung, adipose, skeletal, muscle, neuronal, bone and cartilage conditions. The invention also provides methods for identifying TWEAK agonists or antagonists for the treatment of TWEAK-related conditions. Additionally, the invention provides transgenic animals that express an exogenous DNA encoding a TWEAK polypeptide, or fragments, analogs, or muteins thereof, and methods for using such animals to identify TWEAK agonists or antagonists. The invention further provides methods for diagnosing a disease based on TWEAK expression. The invention also provides methods for affecting cellular differentiation of progenitor cells using TWEAK polypeptides, agonists, or antagonists.
1. A method for treating pulmonary, liver, or cardiac fibrosis in a human subject in need thereof, comprising administering to the subject a therapeutically effective amount of a TWEAK antagonist, wherein the TWEAK antagonist is an antibody, or an antigen-binding fragment thereof, that binds human TWEAK.
2. The method of claim 1 , wherein the fibrosis is liver fibrosis.
3. The method of claim 1 , wherein the fibrosis is cardiac fibrosis.
4. The method of claim 1 , wherein the fibrosis is pulmonary fibrosis.
5. The method of claim 2 , wherein the antibody or antigen-binding fragment thereof is human or humanized.
6. The method of claim 2 , wherein the antibody or antigen-binding fragment thereof is monoclonal or chimeric.
7. The method of claim 2 , wherein a full length antibody is administered.
8. The method of claim 2 , wherein an antigen-binding fragment of the antibody is administered.
9. The method of claim 2 , wherein the TWEAK antagonist is administered to the subject via a route selected from the group consisting of: injection, transmucosal, oral, inhalation, ocular, rectal, stent implantation, topical, parenteral, long acting implantation, sustained release, and aural routes.
10. The method of claim 2 , wherein the TWEAK antagonist is in a delivery formulation selected from the group consisting of: tablets, pills, liposomes, granules, spheres, dragees, capsules, liquids, gels, syrups, slurries, suspensions, stent coatings, and sustained-release formulations.
11. The method of claim 3 , wherein the antibody or antigen-binding fragment thereof is human or humanized.
12. The method of claim 3 , wherein the antibody or antigen-binding fragment thereof is monoclonal or chimeric.
13. The method of claim 3 , wherein a full length antibody is administered.
14. The method of claim 3 , wherein an antigen-binding fragment of the antibody is administered.
15. The method of claim 3 , wherein the TWEAK antagonist is administered to the subject via a route selected from the group consisting of: injection, transmucosal, oral, inhalation, ocular, rectal, stent implantation, topical, parenteral, long acting implantation, sustained release, and aural routes.
16. The method of claim 3 , wherein the TWEAK antagonist is in a delivery formulation selected from the group consisting of: tablets, pills, liposomes, granules, spheres, dragees, capsules, liquids, gels, syrups, slurries, suspensions, stent coatings, and sustained-release formulations.
17. The method of claim 4 , wherein the antibody or antigen-binding fragment thereof is human or humanized.
18. The method of claim 4 , wherein the antibody or antigen-binding fragment thereof is monoclonal or chimeric.
19. The method of claim 4 , wherein a full length antibody is administered.
20. The method of claim 4 , wherein an antigen-binding fragment of the antibody is administered.
21. The method of claim 4 , wherein the TWEAK antagonist is administered to the subject via a route selected from the group consisting of: injection, transmucosal, oral, inhalation, ocular, rectal, stent implantation, topical, parenteral, long acting implantation, sustained release, and aural routes.
22. The method of claim 4 , wherein the TWEAK antagonist is in a delivery formulation selected from the group consisting of: tablets, pills, liposomes, granules, spheres, dragees, capsules, liquids, gels, syrups, slurries, suspensions, stent coatings, and sustained-release formulations.