IP Library › Granted Patent US 11,738,081
Granted Patent B2
US 11,738,081 · App. 16/845,121 · Granted Aug 29, 2023

Polynucleotides encoding IL33 antibodies and methods of using the same

Inventors: Emma S. Cohen (Cambridge, GB); David C. Lowe (Cambridge, GB); Robin Butler (Cambridge, GB); Ian C. Scott (Cambridge, GB); Katherine A. Vousden (Cambridge, GB); Martin D. Strain (Cambridge, GB); Sara Carmen (Cambridge, GB); Elizabeth H. England (Cambridge, GB); Benjamin P. Kemp (Cambridge, GB); David G. Rees (Cambridge, GB); Catherine L. Overed-Sayer (Cambridge, GB); Tomas M. Mustelin (Gaithersburg, MD); Matthew Sleeman (Cambridge, GB); Kirsty Houslay (Cambridge, GB)
Assignee: MEDIMMUNE LIMITED
A61K39/3955A01K67/0278A61P11/06C07K14/54C07K16/244A01K2217/072A01K2227/105A01K2267/03A61K2039/505C07K2317/21C07K2317/33C07K2317/34C07K2317/565C07K2317/567C07K2317/622C07K2317/76C07K2317/92C07K2319/30
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Quick Facts
Patent No.
US 11,738,081
App. No.
16/845,121
Granted
Aug 29, 2023
Kind
B2
Abstract

The present invention provides isolated IL-33 proteins, active fragments thereof and antibodies, antigen binding fragments thereof, against IL-33 proteins. Also provided are methods of modulating cytokine activity, e.g., for the purpose of treating immune and inflammatory disorders.

Claims (15)

1. A polynucleotide encoding an antibody or antigen binding fragment thereof which specifically binds to IL-33, wherein the antibody or antigen binding fragment thereof comprises a variable heavy domain (VH) comprising a VHCDR1 having the sequence of SEQ ID NO: 543, a VHCDR2 having the sequence of SEQ ID NO: 544, and a VHCDR3 having the sequence of SEQ ID NO: 545, and a variable light domain (VL) comprising a VLCDR1 having the sequence of SEQ ID NO: 548, a VLCDR2 having the sequence of SEQ ID NO: 549, and a VLCDR3 having the sequence of SEQ ID NO: 550.

2. The polynucleotide according to claim 1 , wherein the VH and VL of said antibody or antigen-binding fragment thereof comprise amino acid sequences at least 95%, 90%, or 85% identical to SEQ ID NO: 542 and SEQ ID NO: 547, respectively.

3. The polynucleotide according to claim 2 , wherein said antibody or antigen-binding fragment thereof comprises a VH having the sequence of SEQ ID NO: 542 and a VL having the sequence of SEQ ID NO: 547.

4. The polynucleotide according to claim 1 , wherein the VH and VL of said antibody or antigen-binding fragment thereof comprise amino acid sequences at least 95%, 90%, or 85% identical to SEQ ID NO: 616 and SEQ ID NO: 618, respectively.

5. The polynucleotide according to claim 4 , wherein said antibody or antigen-binding fragment thereof comprises a VH having the sequence of SEQ ID NO: 616 and a VL having the sequence of SEQ ID NO: 618.

6. The polynucleotide of any one of claim 1 , 2 , 3 , 4 , or 5 , wherein said antibody or antigen-binding fragment thereof is selected from the group consisting of a human antibody, a chimeric antibody, and a humanized antibody.

7. The polynucleotide of any one of claim 1 , 2 , 3 , 4 , or 5 , wherein said antibody or antigen-binding fragment thereof is selected from the group consisting of a naturally-occurring antibody, an scFv fragment, an Fab fragment, an F(ab′)2 fragment, a minibody, a diabody, a triabody, a tetrabody, and a single chain antibody.

8. The polynucleotide of any one of claim 1 , 2 , 3 , 4 , or 5 , wherein said antibody or antigen-binding fragment thereof is a monoclonal antibody.

9. A vector comprising the polynucleotide of any one of claim 1 , 2 , 3 , 4 , or 5 .

10. A composition comprising the polynucleotide of any one of claim 1 , 2 , 3 , 4 , or 5 .

11. A host cell comprising the polynucleotide of any one of claim 1 , 2 , 3 , 4 , or 5 .

12. A host cell comprising at least a first and a second vector, wherein said first and said second vectors are non-identical, wherein said first vector comprises a polynucleotide encoding SEQ ID NO: 542, which encodes an immunoglobulin heavy chain variable region, and wherein said second vector comprises a polynucleotide encoding SEQ ID NO: 547, which encodes an immunoglobulin light chain variable region.

13. A method of producing an anti-IL33 antibody or antigen-binding fragment thereof, comprising culturing the host cell of claim 12 , and recovering said antibody or antigen-binding fragment thereof.

14. A host cell comprising at least a first and a second vector, wherein said first and said second vectors are non-identical, wherein said first vector comprises a polynucleotide encoding SEQ ID NO: 616, which encodes an immunoglobulin heavy chain variable region, and wherein said second vector comprises a polynucleotide encoding SEQ ID NO: 618, which encodes an immunoglobulin light chain variable region.

15. A method of producing an anti-IL33 antibody or antigen-binding fragment thereof, comprising culturing the host cell of claim 14 , and recovering said antibody or antigen-binding fragment thereof.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 31, 2021
From: MEDIMMUNE, LLC
To: MEDIMMUNE LIMITED
Reel/Frame 055783/0202 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 31, 2021
From: COHEN, EMMA S.; ENGLAND, ELIZABETH H.; REES, DAVID G.; VOUSDEN, KATHERINE A.; LOWE, DAVID C.; BUTLER, ROBIN; SCOTT, IAN C.; STRAIN, MARTIN D.; CARMEN, SARA; KEMP, BENJAMIN P.; OVERED-SAYER, CATHERINE; SLEEMAN, MATTHEW; HOUSLAY, KIRSTY
To: MEDIMMUNE LIMITED
Reel/Frame 055879/0886 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 31, 2021
From: MUSTELIN, TOMAS M.
To: MEDIMMUNE, LLC
Reel/Frame 056495/0767 →
Continuity (3)
Division 15562228
Provisional Application 62140913 · Mar 31, 2015
Related Publication 20200353078A1 · Nov 12, 2020
Cited By (1)
US 12,747,290