IP Library Granted Patent US 10,005,846
Granted Patent B2
US 10,005,846 · App. 14/402,675 · Granted Jun 26, 2018

Anti-transglutaminase 2 antibodies

Inventors: Tim Johnson (Sheffield, GB); Phil Watson (Sheffield, GB); David Matthews (Sheffield, GB); Alex Brown (London, GB)
Assignee: LifeArc
C07K16/40A61K51/1075A61K2039/505C07K2317/34C07K2317/40C07K2317/76
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Quick Facts
Patent No.
US 10,005,846
App. No.
14/402,675
Granted
Jun 26, 2018
Kind
B2
Abstract

The invention provides antibodies and antigen-binding fragments thereof that selectively bind to an epitope within the core region of transglutaminase type 2 (TG2). Novel epitopes within the TG2 core are provided. The invention provides human TG2 inhibitory antibodies and uses thereof, particularly in medicine, for example in the treatment and/or diagnosis of conditions including Celiac disease, scarring, fibrosis-related diseases, neurodegenerative/neurological diseases and cancer.

Claims (15)

1. An antibody, or antigen-binding fragment thereof, that binds human TG2, wherein the antibody or antigen-binding fragment thereof comprises the amino acid sequences set forth in SEQ ID NO: 7 (LCDR1), SEQ ID NO: 17 (LCDR2), SEQ ID NO: 9 (LCDR3), SEQ ID NO: 18 (HCDR1), SEQ ID NO: 15 (HCDR2) and SEQ ID NO: 19 (HCDR3).

2. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof has a light chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 73 and a heavy chain variable region comprising the amino acid sequence set forth in SEQ ID NO: 75.

3. The antibody of claim 1 , wherein the antibody comprises or consists of an intact antibody.

4. The antibody antigen-binding fragment of claim 1 , comprising or consisting of an antigen-binding fragment selected from the group consisting of: an Fv fragment, for example a single chain Fv fragment or a disulphide-bonded Fv fragment; an Fab fragment; and an F(ab′) 2 fragment.

5. The antibody of claim 1 , which is an IgG1, IgG2, IgG3 or IgG4 antibody.

6. The antibody or antigen-binding fragment thereof according to claim 1 further comprising a moiety selected from the group consisting of a readily detectable moiety, a directly cytotoxic moiety, and an indirectly cytotoxic moiety.

7. A pharmaceutical composition comprising the antibody or antigen-binding fragment thereof according to claim 1 in admixture with a pharmaceutically acceptable excipient, adjuvant, diluent or carrier.

8. The pharmaceutical composition according to claim 7 , further comprising one or more further active ingredients.

9. The pharmaceutical composition according to claim 7 , wherein the composition is formulated for intravenous, intramuscular, or subcutaneous delivery to a patient.

10. A kit of parts comprising the antibody or antigen-binding fragment thereof according to claim 1 and a further agent.

11. An in vitro method of reducing or inhibiting human TG2 enzyme activity, the method comprising contacting an antibody or antigen-binding fragment thereof according to claim 1 to a sample comprising human TG2.

12. The method of claim 11 , wherein the sample comprising human TG2 is a tissue sample comprising human TG2 or a cell sample comprising human TG2.

13. A method of reducing or inhibiting TG2 enzyme activity in an individual in need thereof, comprising administering the antibody or antigen-binding fragment thereof according to claim 1 .

14. A method of treating fibrosis in an individual in need thereof, comprising administering an antibody or antigen-binding fragment thereof according to claim 1 to the individual.

15. The method of claim 14 , wherein the fibrosis is selected from the group consisting of liver fibrosis, pulmonary fibrosis, interstitial lung disease, fibrotic lung disease, cardiac fibrosis, myelofibrosis, kidney fibrosis, glomerulosclerosis, and tubulointerstitial fibrosis.

Assignments (2)
CHANGE OF NAME Recorded Sep 5, 2017
From: MEDICAL RESEARCH COUNCIL TECHNOLOGY
To: LIFEARC
Reel/Frame 043760/0808 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2015
From: JOHNSON, TIM; WATSON, PHIL; MATTHEWS, DAVID; BROWN, ALEX
To: MEDICAL RESEARCH COUNCIL TECHNOLOGY
Reel/Frame 034728/0658 →
Priority Claims (1)
GB 1209096.5 · May 24, 2012 · national
Continuity (1)
Related Publication 20150218289A1 · Aug 6, 2015