IP Library Granted Patent US 12,162,952
Granted Patent B2
US 12,162,952 · App. 17/050,353 · Granted Dec 10, 2024

Human-derived anti-(poly-GA) dipeptide repeat (DPR) antibody

Inventors: Jan Grimm (Dübendorf, CH); Fabio Montrasio (Schindellegi, CH); Isin Dalkilic-Liddle (Watertown, MA); Mia Marie Rushe (Everett, MA); Joseph Walter Arndt (Swampscott, MA)
Assignees: Neurimmune AG; Biogen MA Inc.
C07K16/44A61K47/6835A61K49/0002A61K51/10C07K2317/24C07K2317/56C07K2317/565
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Quick Facts
Patent No.
US 12,162,952
App. No.
17/050,353
Granted
Dec 10, 2024
Kind
B2
Abstract

Provided are novel dipeptide repeat (DPR) specific antibodies (e.g., human-derived antibodies) as well as synthetic variants and biotechnological derivatives thereof, capable of binding C9orf72 poly-glycine-alanine DPRs, as well as methods and uses related thereto. The antibody of the present invention can be used in pharmaceutical and diagnostic compositions for DPR protein-targeted immunotherapy and diagnostics.

Claims (43)

1. An antibody capable of binding a dipeptide repeat (DPR) of poly-glycine-alanine (GA) having at least 6 repeats (GA) 6 (SEQ ID NO: 80) as translated from the chromosome 9 open reading frame 72 (C9orf72) gene, or a DPR-binding fragment thereof, wherein the antibody or DPR-binding fragment thereof comprises in its variable region a variable heavy (VH)-complementarity determining region (CDR) 1, a VH-CDR2, a VH-CDR3, a variable light (VL)-CDR1, a VL-CDR2, and a VL-CDR3, wherein:

(a) the VH-CDR1 comprises the amino acid sequence of SEQ ID NO: 3 or the amino acid sequence of SEQ ID NO:78, the VH-CDR2 comprises the amino acid sequence of SEQ ID NO: 13, the VH-CDR3 comprises the amino acid sequence of SEQ ID NO: 5, the VL-CDR 1 comprises the amino acid sequence of SEQ ID NO: 8, the VL-CDR2 comprises the amino acid sequence of SEQ ID NO: 9, and the VL-CDR3 comprises the amino acid sequence of SEQ ID NO: 10;

(b) the VH-CDR1 comprises the amino acid sequence of SEQ ID NO: 3 or the amino acid sequence of SEQ ID NO:78, the VH-CDR2 comprises the amino acid sequence of SEQ ID NO: 16, the VH-CDR3 comprises the amino acid sequence of SEQ ID NO: 5, the VL-CDR 1 comprises the amino acid sequence of SEQ ID NO: 8, the VL-CDR2 comprises the amino acid sequence of SEQ ID NO: 9, and the VL-CDR3 comprises the amino acid sequence of SEQ ID NO: 10;

(c) the VH-CDR1 comprises the amino acid sequence of SEQ ID NO: 3 or the amino acid sequence of SEQ ID NO:78, the VH-CDR2 comprises the amino acid sequence of SEQ ID NO: 19, the VH-CDR3 comprises the amino acid sequence of SEQ ID NO: 5, the VL-CDR 1 comprises the amino acid sequence of SEQ ID NO: 8, the VL-CDR2 comprises the amino acid sequence of SEQ ID NO: 9, and the VL-CDR3 comprises the amino acid sequence of SEQ ID NO: 10;

(d) the VH-CDR1 comprises the amino acid sequence of SEQ ID NO: 3 or the amino acid sequence of SEQ ID NO:78, the VH-CDR2 comprises the amino acid sequence of SEQ ID NO: 22, the VH-CDR3 comprises the amino acid sequence of SEQ ID NO: 5, the VL-CDR 1 comprises the amino acid sequence of SEQ ID NO: 8, the VL-CDR2 comprises the amino acid sequence of SEQ ID NO: 9, and the VL-CDR3 comprises the amino acid sequence of SEQ ID NO: 10; or

(e) the antibody or DPR-binding fragment thereof comprises an amino acid sequence heterologous to the amino acid sequence of SEQ ID NO:2 or heterologous to the amino acid sequence of SEQ ID NO:7, and wherein the VH-CDR1 comprises the amino acid sequence of SEQ ID NO: 3 or the amino acid sequence of SEQ ID NO:78, the VH-CDR2 comprises the amino acid sequence of SEQ ID NO: 4, the VH-CDR3 comprises the amino acid sequence of SEQ ID NO: 5, the VL-CDR1 comprises the amino acid sequence of SEQ ID NO: 8, the VL-CDR2 comprises the amino acid sequence of SEQ ID NO: 9, and the VL-CDR3 comprises the amino acid sequence of SEQ ID NO: 10.

2. The antibody or DPR-binding fragment thereof of claim 1 , which is selected from the group consisting of a single chain Fv fragment (scFv), an F(ab′) fragment, an F(ab) fragment, and an F(ab′) 2 fragment and/or which is a chimeric murine-human or a murinized antibody.

3. The antibody or DPR-binding fragment thereof of claim 1 , which is

(i) detectably labeled with a label selected from the group consisting of an enzyme, a radioisotope, a fluorophore, tag, flag and a heavy metal; or

(ii) attached to a drug.

4. A pharmaceutical composition comprising the antibody or DPR-binding fragment thereof of claim 1 and a pharmaceutically acceptable carrier.

5. A diagnostic composition or kit comprising the antibody or DPR-binding fragment thereof of claim 1 .

6. The antibody or DPR-binding fragment thereof of claim 1 , comprising in its variable region a V H chain and a V L chain, wherein:

(i) the V H chain comprises the amino acid sequence of SEQ ID NO: 2 and the V L chain comprises the amino acid sequence of SEQ ID NO: 24;

(iii) the V H chain comprises the amino acid sequence of SEQ ID NO: 15 and the V L chain comprises the amino acid sequence of SEQ ID NO: 24;

(iv) the V H chain comprises the amino acid sequence of SEQ ID NO: 18 and the V L chain comprises the amino acid sequence of SEQ ID NO: 24; or

(v) the V H chain comprises the amino acid sequence of SEQ ID NO: 21 and the V L chain comprises the amino acid sequence of SEQ ID NO: 24.

7. A method for in vivo detection of or targeting a therapeutic and/or diagnostic agent to poly-GA DPR proteins in a human subject, the method comprising administering to the human subject the antibody or DPR-binding fragment thereof of claim 3 .

8. One or more polynucleotide(s) encoding the antibody or DPR-binding fragment thereof of claim 1 or an immunoglobulin V H or V L chain thereof.

9. One or more vector(s) comprising the polynucleotide(s) of claim 8 .

10. A host cell comprising the polynucleotide(s) of claim 8 .

11. A host cell comprising the vector(s) of claim 9 .

12. A method for preparing an anti-DPR antibody or immunoglobulin chain(s) thereof, said method comprising

(a) culturing the cell of claim 10 ; and

(b) isolating the antibody or immunoglobulin chain(s) thereof from the culture.

13. An antibody capable of binding a dipeptide repeat (DPR) of poly-glycine alanine (GA) having at least 6 repeats (GA) 6 (SEQ ID NO: 80) as translated from the chromosome 9 open reading frame 72 (C9orf72) gene, or a DPR-binding fragment thereof, wherein the antibody or DPR-binding fragment thereof comprises in its variable region the following six complementarity determining regions (CDRs):

(a) a variable heavy (VH)-CDR1 comprising the amino acid sequence of SEQ ID NO: 3,

(b) a VH-CDR2 comprising the amino acid sequence of SEQ ID NO: 13,

(c) a VH-CDR3 comprising the amino acid sequence of SEQ ID NO: 5,

(d) a variable light (VL)-CDR1 comprising the amino acid sequence of SEQ ID NO: 8,

(e) a VL-CDR2 comprising the amino acid sequence of SEQ ID NO: 9, and

(f) a VL-CDR3 comprising the amino acid sequence of SEQ ID NO: 10.

14. The antibody or DPR-binding fragment thereof of claim 13 , comprising in its variable region a V H chain comprising the amino acid sequence of SEQ ID NO: 12.

15. The antibody or DPR-binding fragment thereof of claim 13 , comprising in its variable region a V L chain comprising the amino acid sequence of SEQ ID NO: 24.

16. The antibody or DPR-binding fragment thereof of claim 13 , comprising in its variable region a V H chain comprising the amino acid sequence of SEQ ID NO: 12 and a V L chain comprising the amino acid sequence of SEQ ID NO: 24.

17. A pharmaceutical composition comprising the antibody or DPR-binding fragment thereof of claim 13 and a pharmaceutically acceptable carrier.

18. An antibody capable of binding a dipeptide repeat (DPR) of poly-glycine-alanine (GA) having at least 6 repeats (GA) 6 (SEQ ID NO: 80) as translated from the chromosome 9 open reading frame 72 (C9orf72) gene, or a DPR-binding fragment thereof, wherein the antibody or DPR-binding fragment thereof comprises in its variable region the following six complementarity determining regions (CDRs):

(a) a variable heavy (VH)-CDR1 comprising the amino acid sequence of SEQ ID NO: 78,

(b) a VH-CDR2 comprising the amino acid sequence of SEQ ID NO: 13,

(c) a VH-CDR3 comprising the amino acid sequence of SEQ ID NO: 5,

(d) a variable light (VL)-CDR1 comprising the amino acid sequence of SEQ ID NO: 8,

(e) a VL-CDR2 comprising the amino acid sequence of SEQ ID NO: 9, and

(f) a VL-CDR3 comprising the amino acid sequence of SEQ ID NO: 10.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2021
From: DALKILIC-LIDDLE, ISIN; RUSHE, MIA MARIE; ARNDT, JOSEPH WALTER
To: BIOGEN MA INC.
Reel/Frame 058384/0728 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2021
From: GRIMM, JAN; MONTRASIO, FABIO
To: NEURIMMUNE AG
Reel/Frame 058384/0777 →
Priority Claims (1)
EP 18169888 · Apr 27, 2018 · regional
Continuity (2)
Provisional Application 62772809 · Nov 29, 2018
Related Publication 20220153874A1 · May 19, 2022
Cited By (2)
US 12,638,457 US 12,648,917