IP Library Granted Patent US 12,025,620
Granted Patent B2
US 12,025,620 · App. 16/981,947 · Granted Jul 2, 2024

System and products for improved quantification of ADCC and ADCP activity

Inventors: Michael Tovey (Paris, FR); Christophe Lallemand (Paris, FR)
Assignee: SVAR LIFE SCIENCE AB
G01N33/6854C07K14/70532C07K14/70535C07K16/241C07K16/2863C07K2317/732
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Quick Facts
Patent No.
US 12,025,620
App. No.
16/981,947
Granted
Jul 2, 2024
Kind
B2
Abstract

The present invention relates novel cells and their use in methods for determining the antibody-dependent cell-mediated cytotoxicity (ADCC) or antibody-dependent cell-mediated phagocytosis (ADCP) in a sample.

Claims (26)

1. A cell for the purpose of enhanced dynamic range and increased sensitivity in detection of Antibody-Dependent Cell-mediated Cytotoxicity (ADCC) or Antibody-Dependent Cell-mediated Phagocytosis (ADCP) activity, the cell comprising a viral vector or plasmid encoding (i) a one or more co-stimulatory molecule selected from the group consisting of: CD28, CD137 (4-1BB), CD247 (T3 Zeta chain), CD278 (ICOS), wherein the one or more co-stimulatory molecule is constitutively expressed or over-expressed by the cell; and (ii) a nucleotide sequence SEQ ID NO.:1, wherein SEQ ID NO.: 1 is GGAAGCGAAA ATGAAATTGA CTGGGACTTT CCGGAGGAAA AACTGTTTCA TACAGAAGGC GTGGATGTCC ATATTAGGAT GAGTCAGTGA CGTCAGAGCC TGATTTCCCC GAAATGATGA GCTAG.

2. The cell according to claim 1 , wherein the one or more co-stimulatory molecules are expressed constitutively or over-expressed on the cells.

3. The cell according to claim 1 , wherein the molecular construct further encodes CD16A or CD32.

4. The cell according to claim 1 , wherein a CTLA-4 (CD152) is specifically invalidated.

5. The cell according to claim 1 , wherein the cell is a primary cell or a cell line.

6. The cell according to claim 1 , wherein the cell is an animal cell.

7. The cell according to claim 1 , wherein the molecular construct is an episome or is integrated into the genome of the cell.

8. The cell according to claim 1 , wherein the cell further encodes a first reporter protein.

9. The cell according to claim 8 , wherein the first reporter protein is an enzyme and wherein the enzyme is a luciferase or a fluorescent protein.

10. The cell according to claim 8 , wherein the cell further encodes a second-reporter protein which is different from the first reporter protein.

11. The cell according to claim 1 , wherein the cell further encodes an antigen recognized by an antibody or a Fc fusion protein.

12. A kit, comprising:

i) an effector cell (E), according to claim 1 , and capable of binding to a Fc region of an antibody;

ii) a target cell (T−) in which an endogenous target/antigen to which the antibody is specific is invalidated (mutated) such that the target/antigen is not expressed by the T− cell or is expressed in a non-functional form; and

iii) a target cell (T+) in which the expression of a target to which the antibody is specific is enhanced or is overexpressed together with one or more co-stimulatory molecules including CD80, CD86, CD137L, or (CD278L) ICOSL.

13. A kit according to claim 12 , wherein the cell in ii) and the cell iii) are exactly the same cell identical in all respects except the cell in ii) does not express a specific antigen recognized by the antibody or drug being assayed.

14. The kit according to claim 12 , wherein the target/antigen is one or more of CD20, mTNFα, erbB2, EGFR.

15. The kit according to claim 12 , wherein the kit comprises the cells in i) and iii) in the same vial at the optimal E:T ratio, wherein the ratio between the effector cell in i) and the target cell in iii) (E:T ratio) is in range from about 24:1 to about 2:1, or about 6:1, or about 3:1, or about 1.5:1.

16. A method for quantifying the Antibody-Dependent Cell-mediated Cytotoxicity (ADCC) activity of therapeutic antibodies, the method comprising the steps of;

a) contacting a sample obtained containing an antibody, with effector cell (E) i) according to claim 1 i) and target cells iii) according to claim 1 iii),

b) subtracting the signal obtained in the presence of effector cells (E) i) and cells ii) according to claim 1 ii), in which the drug target has been invalidated, from the signal obtained in the presence of effector cells (E) i) according to claim 1 and target cells iii) according to claim 1 iii),

c) determining the ADCC activity on the basis of the signal relationship as measured in a) and b).

17. A method for quantifying the Antibody-Dependent Cell-mediated Phagocytosis (ADCP) activity of therapeutic antibodies, the method comprising the steps of;

a) contacting a sample obtained containing an antibody, effector cells (E) i) according to claim 1 i) and with target cells iii) according to claim 1 iii),

b) subtracting the signal obtained in the presence of effector cells (E) i) according to claim 1 i) and cells ii) according to claim 1 ii), in which the drug target has been invalidated, from the signal obtained in the presence of effector cells i) according to claim 1 and target cells iii) according to claim 1 iii),

c) determining the ADCP activity on the basis of the signal relationship as measured in a) and b).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2022
From: TOVEY, MICHAEL; LALLEMAND, CHRISTOPHE
To: EURO-DIAGNOSTICA AB
Reel/Frame 058661/0809 →
CHANGE OF NAME Recorded Jan 14, 2022
From: EURO-DIAGNOSTICA AB
To: SVAR LIFE SCIENCE AB
Reel/Frame 058750/0581 →
Priority Claims (1)
EP 18162485 · Mar 19, 2018 · regional
Continuity (1)
Related Publication 20210072256A1 · Mar 11, 2021