IP Library Granted Patent US 10,961,319
Granted Patent B2
US 10,961,319 · App. 15/987,611 · Granted Mar 30, 2021

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 10,961,319
App. No.
15/987,611
Granted
Mar 30, 2021
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. A method of inhibiting human transglutaminase type 2 (TG2)-mediated cross-linking of lysine and glutamine with Nε(γ-glutamyl)lysine isopeptide bonds, the method comprising contacting human TG2 with an antibody that 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 method of claim 1 , wherein the antibody selectively binds to amino acids 304 to 326 of human TG2 (SEQ ID NO: 2).

3. The method of claim 1 , wherein the antibody comprises at least one light chain variable region comprising the amino acid sequence DITMTQSPSSLSASVGDRVTITCKASQDINSYLTWFQQKPGKAPKILIYLVNRLVDGVPSRFSG SGSGQDYALTISSLQPEDFATYYCLQYDDFPYTFGQGTKVEIK (SEQ ID NO: 73); and/or at least one heavy chain variable region comprising the amino acid sequence EVQLLESGGGLVQPGGSLRLSCAASGFTLSTHAMSWVRQAPGKGLEWVATISSGGRSTYYP DSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYFCARLISTYWGQGTLVTVSS (SEQ ID NO: 75), or

an amino acid sequence having at least 90% identity with the amino acid sequence set forth in SEQ ID NO: 73 or the amino acid sequence set forth in SEQ ID NO: 75.

4. The method of claim 1 , wherein the antibody has:

a light chain variable region comprising the sequence

DITMTQSPSSLSASVGDRVTITCKASQDINSYLTWFQQKPGKAPKILIYLVNRLVDGVPS RFSGSGSGQDYALTISSLQPEDFATYYCLQYDDFPYTFGQGTKVEIK (SEQ ID NO: 73), and a heavy chain variable region comprising the sequence

EVQLLESGGGLVQPGGSLRLSCAASGFTLSTHAMSWVRQAPGKGLEWVATISSGGRS TYYPDSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYFCARLISTYWGQGTLVTVSS (SEQ ID NO: 75).

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

6. The method of claim 1 , wherein the antibody is an antigen-binding fragment selected from the group consisting of: a Fv, a single chain Fv (scFv) or a disulfide-bonded Fv; a Fab; and a Fab-like, a Fab′ or a F(ab) 2 .

7. The method according to claim 1 , wherein the antibody thereof does not inhibit TG1, TG3, TG13 and/or TG7 activity.

8. The method of claim 1 , wherein the antibody is an IgG1, IgG2, IgG3 or IgG4.

9. The method of claim 1 , that is an in vivo method.

10. A method of treating fibrosis in an individual comprising administering an antibody or antigen-binding fragment thereof that 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).

11. A method of inhibiting human transglutaminase type 2 (TG2)-mediated cross-linking of lysine and glutamine with Nε(γ-glutamyl)lysine isopeptide bonds in an individual, the method comprising administering to an individual in need thereof an antibody or antigen-binding fragment thereof that 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).

Assignments (1)
CHANGE OF NAME Recorded Mar 16, 2020
From: MEDICAL RESEARCH COUNCIL TECHNOLOGY
To: LIFEARC
Reel/Frame 052389/0665 →
Priority Claims (1)
GB 1209096 · May 24, 2012 · national
Continuity (2)
Continuation 14402675
Related Publication 20180355060A1 · Dec 13, 2018