Modified IL-4 mutein receptor antagonists
This invention relates to modified IL-4 mutein receptor antagonists comprising an IL-4 mutein receptor antagonist coupled to polyethylene glycol. Related formulations and dosages and methods of administration thereof for therapeutic purposes are also provided. These modified IL-4 mutein receptor antagonists, compositions and methods provide a treatment option for those individuals afflicted with a respiratory disorder such as asthma by inhibiting IL-4 and IL-13-mediated airway hyperresponsiveness and eosinophilia. More particularly, these antagonists have an increased duration of effect versus unmodified IL-4RA by virtue of a greater plasma half-life.
1. A modified IL-4 mutein receptor antagonist coupled to a non-protein polymer at an amino acid residue at position 28, 36, 37, 38, 104, 105, or 106 of IL-4, wherein the amino acids at positions 13, 121 and 124 are aspartic acid, wherein the amino acids are numbered according to wild type human IL-4, and wherein the non-protein polymer is polyethylene glycol, polypropylene glycol or a polyoxyalkylene.
2. The modified IL-4 mutein receptor antagonist of claim 1 , wherein the non-protein polymer is coupled at an amino acid residue at position 37, 38, or 104 of IL-4.
3. The modified IL-4 mutein receptor antagonist of claim 1 , wherein the antagonist consists of the amino acid sequence as set forth in SEQ ID NO: 33.
4. The modified IL-4 mutein receptor antagonist of claim 1 , wherein the non-protein polymer is polyethylene glycol.
5. The modified IL-4 mutein receptor antagonist of claim 4 , wherein the polyethylene glycol is linear.
6. The modified IL-4 mutein receptor antagonist of claim 4 , wherein the polyethylene glycol is branched.
7. The modified IL-4 mutein receptor antagonist of claim 6 , wherein the polyethylene glycol is about 3 kD to 50 kD.
8. The modified IL-4 mutein receptor antagonist of claim 7 , wherein the polyethylene glycol is 40 kD.
9. A pharmaceutical composition comprising:
a) the modified IL-4 mutein receptor antagonist of claim 1 ; and
b) a pharmaceutically acceptable carrier.
10. A pharmaceutical composition comprising:
a) the modified IL-4 mutein receptor antagonist of claim 8 ; and
b) a pharmaceutically acceptable carrier.
11. The modified IL-4 mutein receptor antagonist of claim 1 , wherein the modified mutein receptor antagonist binds to the IL-4 receptor alpha chain with a K D of about 0.1 nM to about 10 μM, about 0.5 nM to about 1 μM, or about 1.0 nM to about 100 nM.
12. The modified IL-4 mutein receptor antagonist of claim 1 , wherein the modified IL-4 mutein receptor antagonist inhibits the proliferative response of TF-1 cells to IL-4 with an IC 50 of about 0.1 nM to about 10 μM, about 0.5 nM to about 1 μM, or about 1.0 nM to about 100 nM.
13. The modified IL-4 mutein receptor antagonist of claim 1 , wherein the modified IL-4 mutein receptor antagonist inhibits the proliferative response of TF-1 cells to IL-13 with an IC 50 of about 0.1 nM to about 10 μM, about 0.5 nM to about 1 μM, or about 1.0 nM to about 100 nM.
14. The modified IL-4 mutein receptor antagonist of claim 1 , wherein the modified IL-4 mutein receptor antagonist inhibits the proliferative response of human B cells to IL-4 with an IC 50 of about 0.1 nM to about 10 μM, about 0.5 nM to about 1 μM, or about 1.0 nM to about 100 nM.
15. The modified IL-4 mutein receptor antagonist of claim 1 , wherein the modified IL-4 mutein receptor antagonist inhibits the proliferative response of human T cells to IL-4 with an IC 50 of about 0.1 nM to about 10 μM, about 0.5 nM to about 1 μM, or about 1.0 nM to about 100 nM.
16. The modified IL-4 mutein receptor antagonist of claim 1 , wherein the modified IL-4 mutein receptor antagonist has a plasma half-life which is at least about 2-10 fold greater than that of an unmodified IL-4 receptor antagonist.
17. The modified IL-4 mutein receptor antagonist of claim 1 , wherein the modified IL-4 mutein receptor antagonist has a plasma half-life which is at least about 10-100 fold greater than that of an unmodified IL-4 receptor antagonist.