ANTI-CD137 ANTIBODY AS AN AGENT IN THE TREATMENT OF INFLAMMATORY CONDITIONS
The present invention relates to the treatment of inflammatory conditions including atherosclerosis and sepsis. In particular, the invention relates to treatment of these conditions using antibodies.
1 . A method of treating an inflammatory condition comprising administering to a mammal a therapeutically effective amount of a recombinant aglycosylated CD137 antibody or a prodrug thereof or a pharmaceutically acceptable salt thereof.
2 . The method of claim 1 , wherein the antibody is aglycosylated in the constant region of the antibody.
3 . The method of claim 1 , wherein the antibody is aglycosylated in the variable region and the constant region of the antibody.
4 . The method of claim 1 , wherein the inflammatory condition is sepsis.
5 . The method of claim 1 , wherein the inflammatory condition is atherosclerosis.
6 . The method of claim 1 , wherein the recombinant aglycosylated CD137 antibody is encoded by a transgene DNA construct in a bioreactor organism, said transgene construct comprising a polypeptide domain.
7 . The method of claim 6 , wherein the DNA construct is actuated by at least one beta-casein promoter.
8 . The method of claim 6 , wherein the bioreactor organism is a transgenic ungulate.
9 . The method of claim 1 , wherein the therapeutically effective amount is about 0.01 mg/kg/day to about 50 mg/kg/day.
10 . The method of claim 1 , wherein the mammal is a human.
11 . The method of claim 1 , wherein the aglycosylated CD137 antibody is a chimeric antibody.
12 . The method of claim 1 , wherein the aglycosylated CD137 antibody is a humanized antibody.
13 . The method of claim 1 , wherein the aglycosylated CD137 antibody is a fully humanized antibody.
14 . A method of treating atherosclerosis comprising administering to a human a therapeutically effective amount of an aglycosylated CD137 antibody.
15 . The method of claim 14 , wherein the therapeutically effective amount is about 0.01 mg/kg.day to about 50 mg/kg/day.
16 . The method of claim 14 , wherein the CD137 antibody is aglycosylated in the constant region of the antibody.
17 . The method of claim 14 , wherein the CD137 antibody is aglycosylated in the variable region and the constant region of the antibody.
18 . The method of claim 14 , wherein the aglycosylated CD137 antibody is a chimeric antibody.
19 . The method of claim 14 , wherein the aglycosylated CD137 antibody is a humanized antibody.
20 . The method of claim 14 , wherein the aglycosylated CD137 antibody is a fully human antibody.