IP Library Granted Patent US 9,494,575
Granted Patent B2
US 9,494,575 · App. 12/671,690 · Granted Nov 15, 2016

Cells screening method

Inventors: Aishun Jin (Toyama, JP); Hiroyuki Kishi (Toyama, JP); Atsushi Muraguchi (Toyama, JP); Tsutomu Obata (Takaoka, JP)
Assignees: TOYAMA PREFECTURE; VALNEVA
G01N33/5047
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Quick Facts
Patent No.
US 9,494,575
App. No.
12/671,690
Granted
Nov 15, 2016
Kind
B2
Abstract

Provided are a method and means permitting the simultaneous measurement of the reactive properties of more than 10,000 of antigen-stimulated lymphocytes being held on a chip. A microwell array comprises multiple wells capturing single cells and a coating layer on a principal surface around the wells containing a substance capable of binding to a substance produced by the cells in the wells. A method for screening a target cell comprises: causing specimen cells and a cell culture broth to be contained in the wells of the microwell array; culturing the cells in a state permitting the diffusion of substances from the wells into the coating layer; feeding a label substance binding specifically to a substance produced by a target cell onto the coating layer; and detecting the substance produced by the target cell by the label substance binding around the well to specify the target cell.

Claims (39)

1. A method of screening for a target cell, comprising:

causing specimen cells and a cell culture broth to be contained in at least a portion of the wells of a microwell array comprising multiple wells, each well being of a size permitting the entry of only a single cell therein, on one of the principal surfaces of a base member, wherein a coating layer of a binding substance having the ability to bind to at least a portion of a substance produced by a target cell is present only around the wells of said principal surface;

immersing the coating layer and the wells in the culture broth and culturing the cells in a state permitting the diffusion of said substance produced by said target cell in the culture broth from the wells into the coating layer;

after optionally removing the culture broth, feeding a label substance binding specifically to said substance produced by said target cell present among the specimen cells onto the coating layer; and

detecting the binding of said substance produced by said target cell to said binding substance by means of said label substance in order to specify the well containing said target cell.

2. The screening method according to claim 1 , wherein the cells present among the specimen cells include cells that have been stimulated with a desired antigen in advance and are in a state capable of producing a substance.

3. The screening method according to claim 1 , wherein the specimen cells include immunoglobulin-producing cells or cytokine-producing cells.

4. The screening method according to claim 1 , wherein the specimen cells include immunoglobulin-producing cells, said binding substance is an anti-immunoglobulin antibody or antigen, and the target cell is an antigen-specific immunoglobulin-producing cell.

5. The screening method according to claim 4 , wherein the detection of the presence or absence of the binding is conducted using antigen or an antibody to the immunoglobulin that is produced.

6. The screening method according to claim 1 , wherein the specimen cells include cytokine-producing cells, said binding substance is an anti-cytokine antibody or a cytokine receptor, and the target cell is an antigen-specific cytokine-producing cell.

7. The screening method according to claim 6 , wherein the detection of the presence or absence of the binding is conducted using an antibody to the cytokine produced or a cytokine receptor.

8. The screening method according to claim 4 or 6 , wherein the immunoglobulin-producing cells and cytokine-producing cells are natural cells, hybridomas, or cell strains.

9. A method for obtaining a target cell producing a given substance, wherein said target cell is from a group of cells containing specimen cells, comprising the steps of:

causing said specimen cells and a cell culture broth to be contained in at least a portion of wells of a microwell array,

wherein said microwell array comprises multiple wells on a principal surface of a base member, each well being of a size permitting the entry of only a single cell therein,

wherein a coating layer of a binding substance having the ability to bind to at least a portion of said substance produced by said target cell is bound on said principal surface, and

wherein said binding substance is present only around the wells on said principal surface;

immersing the coating layer and the wells in the culture broth and culturing the cells in a state permitting the diffusion of said substance produced by said target cell in the culture broth from the wells into the coating layer;

after optionally removing the culture broth, feeding a label substance binding specifically to said substance produced by said target cell present among the specimen cells onto the coating layer;

detecting the binding of said substance produced by said target cell to said binding substance by means of said label substance in order to specify the well containing said target cell; and

recovering said target cell from a well thus specified.

10. The method according to claim 9 , wherein said target cell is a specific immunoglobulin-producing cell or specific cytokine-producing cell.

11. The method according to claim 9 , wherein the cells present among the specimen cells include cells that have been stimulated with a desired antigen prior to introduction into the wells of said microarray and are in a state capable of producing a substance.

12. The method according to claim 9 , wherein said target cell is an antigen-specific immunoglobulin-producing cell and said binding substance is an antigen or an anti-immunoglobulin antibody.

13. The method according to claim 12 , wherein said label substance is said specific antigen or an anti-immunoglobulin antibody.

14. The method according to claim 9 , wherein said target cell is an antigen-specific cytokine-producing cell and said binding substance is an antibody to said cytokine, or a cytokine receptor.

15. The method according to claim 14 , wherein said label substance is an antibody to said cytokine, or a cytokine receptor.

16. The method according to claim 10 , wherein said immunoglobulin-producing cells or cytokine-producing cells are selected from the group consisting of primary cells, hybridomas, and cell lines.

17. The method according to claim 9 , wherein the multiple wells are recesses formed within the principal surface of the base member.

18. The method according to claim 9 , wherein said target cell is a mammalian cell.

19. The method according to claim 9 , wherein the wells have a diameter of 4 micrometers to 15 micrometers.

20. The method according to claim 9 , wherein the wells have a diameter in a range of 0.5 to 2 times a diameter of the cell.

21. A method for obtaining a target cell producing a given substance, wherein said target cell is from a group of cells containing specimen cells, comprising the steps of:

providing a microwell array wherein said microwell array comprises multiple wells and is formed on a principal surface of a base member, each well being of a size permitting the entry of only a single cell therein, said microwell array comprising a coating layer of a binding substance having the ability to bind to at least a portion of said substance produced by said target cell on said principal surface around the wells;

causing said specimen cells and a cell culture broth to be contained in at least a portion of the wells with the coating layer around the wells;

immersing the coating layer and the wells in the culture broth and culturing the cells in a state permitting the diffusion of said substance produced by said target cell in the culture broth from the wells into the coating layer;

after optionally removing the culture broth, feeding a label substance binding specifically to said substance produced by said target cell present among the specimen cells onto the coating layer;

detecting the binding of said substance produced by said target cell to said binding substance by means of said label substance in order to specify the well containing said target cell; and

recovering said target cell from a well thus specified.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 3, 2020
From: VALNEVA
To: BLINK BIOMEDICAL SAS
Reel/Frame 052830/0316 →
CHANGE OF NAME Recorded Jan 17, 2014
From: VIVALIS
To: VALNEVA
Reel/Frame 031990/0648 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2011
From: SC WORLD INC.
To: VIVALIS
Reel/Frame 027049/0284 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 12, 2011
From: JIN, AISHUN; KISHI, HIROYUKI; MURAGUCHI, ATSUSHI; OBATA, TSUTOMU
To: TOYAMA PREFECTURE; SC WORLD INC.
Reel/Frame 026739/0753 →
Priority Claims (1)
JP 2007-201493 · Aug 2, 2007 · national
Continuity (1)
Related Publication 20110294678A1 · Dec 1, 2011