US2013216542A1PendingUtilityA1

Variable region sequences of il-31 monoclonal antibodies and methods of use

60
Assignee: SIADAK ANTHONY WPriority: May 6, 2005Filed: Dec 19, 2011Published: Aug 22, 2013
Est. expiryMay 6, 2025(expired)· nominal 20-yr term from priority
A61K 47/60C07K 2317/24C07K 2317/52C07K 2317/56C07K 16/244C07K 2317/30C07K 2317/565C07K 2317/34C07K 2317/92C07K 2317/76A61K 2039/505
60
PatentIndex Score
0
Cited by
0
References
0
Claims

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 provides the hybridomas that generate the monoclonal antibodies and the amino acid sequences of the variable regions of the monoclonal antibodies and chimeric antibodies comprising the amino acid sequences of the light and heavy chain variable regions.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of reducing pruritis in a mammal comprising administering to the mammal a therapeutically effective amount of a monoclonal antibody or antigen-binding fragment thereof which is capable of specifically binding to a polypeptide consisting of amino acid residues 27 to 164 of SEQ ID NO:2, wherein the monoclonal antibody or antigen-binding fragment comprises a light chain variable region comprising CDRs LCDR1, LCDR2, and LCDR3 and a heavy chain variable region comprising CDRs HCDR1, HCDR2, and HCDR3, wherein
 LCDR1 has the amino acid sequence of SEQ ID NO:54;   LCDR2 has the amino acid sequence of SEQ ID NO:55;   LCDR3 has the amino acid sequence of SEQ ID NO:56;   HCDR1 has the amino acid sequence of SEQ ID NO:51;   HCDR2 has the amino acid sequence of SEQ ID NO:52; and   HCDR3 has the amino acid sequence of SEQ ID NO:53;   
       wherein the monoclonal antibody or antigen-binding fragment inhibits signaling by the polypeptide through its cognate receptor, and wherein after administration of the monoclonal antibody or antigen-binding fragment the pruritus is reduced. 
     
     
         2 . The monoclonal antibody or antigen-binding fragment of  claim 1 , wherein the monoclonal antibody or antigen-binding fragment is humanized. 
     
     
         3 . The antigen-binding fragment of  claim 1 , wherein the antigen-binding fragment is a Fab, Fab′, F(ab′) 2  or a single chain Fv. 
     
     
         4 . The monoclonal antibody or antigen-binding fragment of  claim 1 , wherein the light chain variable region comprises the amino acid residues of SEQ ID NO:8. 
     
     
         5 . The monoclonal antibody or antigen-binding fragment of  claim 1 , wherein the heavy chain variable region comprises the amino acid residues of SEQ ID NO:9. 
     
     
         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 comprising administering to the mammal a therapeutically effective amount of a monoclonal antibody or antigen-binding fragment thereof which is capable of specifically binding to a polypeptide consisting of amino acid residues 27 to 164 of SEQ ID NO:2, wherein the monoclonal antibody or antigen-binding fragment comprises a light chain variable region comprising CDRs LCDR1, LCDR2, and LCDR3 and a heavy chain variable region comprising CDRs HCDR1, HCDR2, and HCDR3, wherein
 LCDR1 has the amino acid sequence of SEQ ID NO:54;   LCDR2 has the amino acid sequence of SEQ ID NO:55;   LCDR3 has the amino acid sequence of SEQ ID NO:56;   HCDR1 has the amino acid sequence of SEQ ID NO:51;   HCDR2 has the amino acid sequence of SEQ ID NO:52; and   HCDR3 has the amino acid sequence of SEQ ID NO:53;   
       wherein the monoclonal antibody or antigen-binding fragment inhibits signaling by the polypeptide through its cognate receptor, and wherein after administration of the monoclonal antibody or antigen-binding fragment the inflammation is reduced. 
     
     
         7 . The monoclonal antibody or antigen-binding fragment of  claim 6 , wherein the monoclonal antibody or antigen-binding fragment is humanized. 
     
     
         8 . The antigen-binding fragment of  claim 6 , wherein the antigen-binding fragment is a Fab, Fab′, F(ab′) 2  or a single chain Fv. 
     
     
         9 . The monoclonal antibody or antigen-binding fragment of  claim 6 , wherein the light chain variable region comprises the amino acid residues of SEQ ID NO:8. 
     
     
         10 . The monoclonal antibody or antigen-binding fragment of  claim 6 , wherein the heavy chain variable region comprises the amino acid residues of SEQ ID NO:9.

Cited by (0)

No later patents cite this yet.

References (0)

No backward citations on record.