IP Library Granted Patent US 10,287,348
Granted Patent B2
US 10,287,348 · App. 15/014,828 · Granted May 14, 2019

Antigen binding proteins capable of binding thymic stromal lymphopoietin

Inventors: Michael R. Comeau (Bainbridge Island, WA); James F. Smothers (Quincy, MA); Bo-Rin P. Yoon (Seattle, WA); Christopher Mehlin (Seattle, WA)
Assignee: Amgen Inc.
C07K16/24C07K16/244A61K39/395A61K39/3955A61K2039/505C07K2317/21C07K2317/24C07K2317/33C07K2317/55C07K2317/565C07K2317/622C07K2317/626C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 10,287,348
App. No.
15/014,828
Granted
May 14, 2019
Kind
B2
Abstract

The present disclosure provides compositions and methods relating to antigen binding proteins which bind to human thymic stromal lymphopoietin (TSLP), including antibodies. In particular embodiments, the disclosure provides fully human, humanized and chimeric anti-TSLP antibodies and derivatives of such antibodies. The disclosure further provides nucleic acids encoding such antibodies and antibody fragments and derivatives, and methods of making and using such antibodies including methods of treating and preventing TSLP-related inflammatory and fibrotic disorders.

Claims (31)

1. An isolated antibody or antigen binding fragment thereof that binds a wild-type TSLP polypeptide consisting of amino acids 29-159 as set forth in SEQ ID NO:2 with a greater affinity than the antibody or antigen binding fragment thereof binds to a mutated TSLP polypeptide consisting of amino acids 29-159 as set forth in SEQ ID NO:2 but comprising a single amino acid substitution selected from the group consisting of K12E, D22R, R122E, N124E, R125E, and K129E,

wherein said antibody or antigen binding fragment thereof comprises

A.

a. a light chain variable domain comprising:

i. a light chain CDR1 sequence comprising the amino acid sequence of SEQ ID NO:13;

ii. a light chain CDR2 sequence comprising the amino acid sequence of SEQ ID NO:60; and

iii. a light chain CDR3 sequence comprising the amino acid sequence of SEQ ID NO:105; and

b. a heavy chain variable domain comprising:

i. a heavy chain CDR1 sequence comprising the amino acid sequence of SEQ ID NO:145;

ii. a heavy chain CDR2 sequence comprising the amino acid sequence of SEQ ID NO:173, and

iii. a heavy chain CDR3 sequence comprising the amino acid sequence of SEQ ID NO:212; or

B.

a. a light chain variable domain sequence selected from the group consisting of:

i. a sequence of amino acids at least 80% identical to SEQ ID NO:363;

ii. a sequence of amino acids encoded by a polynucleotide sequence that is at least 80% identical to SEQ ID NO:362;

and

b. a heavy chain variable domain sequence selected from the group consisting of:

i. a sequence of amino acids that is at least 80% identical to SEQ ID NO:361;

ii. a sequence of amino acids encoded by a polynucleotide sequence that is at least 80% identical to SEQ ID NO:360,

wherein the light chain variable domain sequences of (B) comprise the light chain CDR1-3 sequences of (A) and wherein the heavy chain variable domain sequences of (B) comprise heavy chain CDR1-3 sequences of (A).

2. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein the single amino acid substitution in wild-type TSLP consists of K12E.

3. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein the single amino acid substitution in wild-type TSLP consists of D22R.

4. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein the single amino acid substitution in wild-type TSLP consists of R122E.

5. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein the single amino acid substitution in wild-type TSLP consists of N124E.

6. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein the single amino acid substitution in wild-type TSLP consists of R125E.

7. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein the single amino acid substitution in wild-type TSLP consists of K129E.

8. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein the antibody or antigen binding fragment thereof has a lower binding affinity for any two or more members of a group of mutated TSLP, wherein the group of mutated TSLP are selected from those mutated TSLP consisting of amino acids 29-159 as set forth in SEQ ID NO:2 but comprising a single amino acid substitution selected from the group consisting of K12E, D22R, R122E, N124E, R125E, and K129E compared to the binding affinity for the wild-type TSLP.

9. The isolated antigen binding protein of claim 8 , wherein antibody or antigen binding fragment thereof has a lower binding affinity for all members of the group of mutated TSLP compared to the binding affinity for the wild-type TSLP.

10. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein said antibody or antigen binding fragment thereof is selected from the group consisting of a human antibody, a chimeric antibody, a monoclonal antibody, a recombinant antibody, an antigen-binding antibody fragment, a single chain antibody, a monomeric antibody, a diabody, a triabody, a tetrabody, a Fab fragment, an IgD antibody, an IgE antibody, an IgM antibody, an IgG1 antibody, an IgG2 antibody, an IgG3 antibody, and an IgG4 antibody.

11. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein said antibody is a human antibody.

12. A composition comprising the antibody of claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2018
From: COMEAU, MICHAEL R.; SMOTHERS, JAMES F.; YOON, BO-RIN P.; MEHLIN, CHRISTOPHER
To: AMGEN INC.
Reel/Frame 046716/0431 →
Continuity (6)
Division 13438739 · Apr 3, 2012
Division 13185021 · Jul 18, 2011
Division 12231944 · Sep 8, 2008
Provisional Application 61091676 · Aug 25, 2008
Provisional Application 60971178 · Sep 10, 2007
Related Publication 20160152700A1 · Jun 2, 2016
Cited By (1)
US 12,686,714