IP Library Granted Patent US 8,017,122
Granted Patent B2
US 8,017,122 · App. 12/420,747 · Granted Sep 13, 2011

Methods of using IL-31 monoclonal antibodies to reduce inflammation

Assignee: ZymoGenetics, Inc.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,017,122
App. No.
12/420,747
Granted
Sep 13, 2011
Kind
B2
Abstract

The present invention relates to methods of treating pruritic diseases, including but not limited to Contact dermatitis, Atopic Dermatitis, Drug induced delayed type cutaneous allergic reactions, Toxic epidermal necrolysis, Cutaneous T cell Lymphoma, Bullous pemphigoid, Alopecia wereata, Vitiligo, Acne Rosacea, Prurigo nodularis, Scleroderma, Herpes simplex virus, or combination thereof by administering IL-31 monoclonal antibodies. The invention further provides the hybridomas that generate the monoclonal antibodies.

Claims (74)

1. A method of reducing inflammation in a mammal with a skin or epidermal condition having increased infiltration of cutaneous lymphocyte antigen (CLA+) T cells comprising administering to the mammal a monoclonal antibody or antibody fragment thereof, wherein the monoclonal antibody is produced by the hybridoma deposited with the American Type Culture Collection having the ATCC Patent Deposit Designation selected from the group consisting of:

a) ATCC Patent Deposit Designation PTA-6815;

b) ATCC Patent Deposit Designation PTA-6816;

c) ATCC Patent Deposit Designation PTA-6829;

d) ATCC Patent Deposit Designation PTA-6830;

e) ATCC Patent Deposit Designation PTA-6831;

f) ATCC Patent Deposit Designation PTA-6871;

g) ATCC Patent Deposit Designation PTA-6872;

h) ATCC Patent Deposit Designation PTA-6875; and

i) ATCC Patent Deposit Designation PTA-6873,

wherein the polypeptide consists of amino acid residues 27 to 164 of SEQ ID NO: 2, and wherein the inflammation is reduced.

2. The method according to claim 1 , wherein the monoclonal antibody or antibody fragment neutralizes the interaction of the polypeptide with a receptor polypeptide comprising the amino acid sequence of SEQ ID NO:5.

3. The method of claim 1 , wherein the monoclonal antibody or antibody fragment comprises a radionuclide, enzyme, substrate, cofactor, fluorescent marker, chemiluminescent marker, peptide tag, magnetic particle, or toxin.

4. The method of claim 1 , wherein the monoclonal antibody or antibody fragment comprises PEG.

5. The method of claim 1 , wherein the monoclonal antibody or antibody fragment is selected from the group consisting of:

a) a chimeric antibody or antibody fragment;

b) a humanized antibody or antibody fragment; and

c) a Fab molecule; and

d) a F(ab′) 2 molecule.

6. A method of reducing inflammation in a mammal with a skin or epidermal condition having increased infiltration of cutaneous lymphocyte antigen (CLA+) T cells comprising administering to the mammal a monoclonal antibody or antibody fragment thereof that is capable of inhibiting the binding of a polypeptide to a receptor, wherein the monoclonal antibody is produced by the hybridoma deposited with the American Type Culture Collection having the ATCC Patent Deposit Designation selected from the group consisting of:

a) ATCC Patent Deposit Designation PTA-6815;

b) ATCC Patent Deposit Designation PTA-6816;

c) ATCC Patent Deposit Designation PTA-6829;

d) ATCC Patent Deposit Designation PTA-6830;

e) ATCC Patent Deposit Designation PTA-6831;

f) ATCC Patent Deposit Designation PTA-6871;

g) ATCC Patent Deposit Designation PTA-6872;

h) ATCC Patent Deposit Designation PTA-6875; and

i) ATCC Patent Deposit Designation PTA-6873,

wherein the polypeptide consists of amino acid residues 27 to 164 of SEQ ID NO: 2, wherein the receptor is the IL-31RA receptor of SEQ ID NO: 5, and wherein the inflammation is reduced.

7. The method of claim 6 , wherein the monoclonal antibody or antibody fragment comprises a radionuclide, enzyme, substrate, cofactor, fluorescent marker, chemiluminescent marker, peptide tag, magnetic particle, or toxin.

8. The method of claim 6 , wherein the monoclonal antibody or antibody fragment comprises PEG.

9. The method of claim 6 , wherein the monoclonal antibody or antibody fragment is selected from the group consisting of:

a) a chimeric antibody or antibody fragment;

b) a humanized antibody or antibody fragment; and

c) a Fab molecule; and

d) a F(ab′) 2 molecule.

10. A method of reducing pruritis in a mammal with a skin or epidermal condition having increased infiltration of cutaneous lymphocyte antigen (CLA+) T cells comprising administering to the mammal a monoclonal antibody or antibody fragment thereof, wherein the monoclonal antibody is produced by the hybridoma deposited with the American Type Culture Collection having the ATCC Patent Deposit Designation selected from the group consisting of:

a) ATCC Patent Deposit Designation PTA-6815;

b) ATCC Patent Deposit Designation PTA-6816;

c) ATCC Patent Deposit Designation PTA-6829;

d) ATCC Patent Deposit Designation PTA-6830;

e) ATCC Patent Deposit Designation PTA-6831;

f) ATCC Patent Deposit Designation PTA-6871;

g) ATCC Patent Deposit Designation PTA-6872;

h) ATCC Patent Deposit Designation PTA-6875; and

i) ATCC Patent Deposit Designation PTA-6873,

wherein the polypeptide consists of amino acid residues 27 to 164 of SEQ ID NO: 2, and wherein the pruritis is reduced.

11. The method according to claim 10 , wherein the monoclonal antibody or antibody fragment neutralizes the interaction of the polypeptide with a receptor polypeptide comprising the amino acid sequence of SEQ ID NO:5.

12. The method of claim 10 , wherein the monoclonal antibody or antibody fragment comprises a radionuclide, enzyme, substrate, cofactor, fluorescent marker, chemiluminescent marker, peptide tag, magnetic particle, or toxin.

13. The method of claim 10 , wherein the monoclonal antibody or antibody fragment comprises PEG.

14. The method of claim 10 , wherein the monoclonal antibody or antibody fragment is selected from the group consisting of:

a) a chimeric antibody or antibody fragment;

b) a humanized antibody or antibody fragment; and

c) a Fab molecule; and

d) a F(ab′) 2 molecule.

15. A method of reducing pruritis in a mammal with a skin or epidermal condition having increased infiltration of cutaneous lymphocyte antigen (CLA+) T cells comprising administering to the mammal a monoclonal antibody or antibody fragment thereof that is capable of inhibiting the binding of a polypeptide to a receptor, wherein the monoclonal antibody is produced by the hybridoma deposited with the American Type Culture Collection having the ATCC Patent Deposit Designation selected from the group consisting of:

a) ATCC Patent Deposit Designation PTA-6815;

b) ATCC Patent Deposit Designation PTA-6816;

c) ATCC Patent Deposit Designation PTA-6829;

d) ATCC Patent Deposit Designation PTA-6830;

e) ATCC Patent Deposit Designation PTA-6831;

f) ATCC Patent Deposit Designation PTA-6871;

g) ATCC Patent Deposit Designation PTA-6872;

h) ATCC Patent Deposit Designation PTA-6875; and

i) ATCC Patent Deposit Designation PTA-6873,

wherein the polypeptide consists of amino acid residues 27 to 164 of SEQ ID NO: 2, wherein the receptor is the IL-31RA receptor of SEQ ID NO: 5, and wherein the pruritis is reduced.

16. The method of claim 15 , wherein the monoclonal antibody or antibody fragment comprises a radionuclide, enzyme, substrate, cofactor, fluorescent marker, chemiluminescent marker, peptide tag, magnetic particle, or toxin.

17. The method of claim 15 , wherein the monoclonal antibody or antibody fragment comprises PEG.

18. The method of claim 15 , wherein the monoclonal antibody or antibody fragment is selected from the group consisting of:

a) a chimeric antibody or antibody fragment;

b) a humanized antibody or antibody fragment; and

c) a Fab molecule; and

d) a F(ab′) 2 molecule.

Continuity (5)
Division 11430066 · May 8, 2006
Provisional Application 60678918 · May 6, 2005
Provisional Application 60696251 · Jul 1, 2005
Provisional Application 60711600 · Aug 26, 2005
Related Publication 20090220417A1 · Sep 3, 2009