IP Library Granted Patent US 8,642,835
Granted Patent B2
US 8,642,835 · App. 13/404,075 · Granted Feb 4, 2014

ADAM6 mice

Inventors: Lynn MacDonald (White Plains, NY); Sean Stevens (San Francisco, CA); Andrew J. Murphy (Croton-on-Hudson, NY)
Assignee: Regeneron Pharmaceuticals, Inc.
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Quick Facts
Patent No.
US 8,642,835
App. No.
13/404,075
Granted
Feb 4, 2014
Kind
B2
Abstract

Mice are provided that comprise a reduction or deletion of ADAM6 activity from an endogenous ADAM6 locus, or that lack an endogenous locus encoding a mouse ADAM6 protein, wherein the mice comprise a sequence encoding an ADAM6 or ortholog or homolog or fragment thereof that is functional in a male mouse. In one embodiment, the sequence is an ectopic ADAM6 sequence or a sequence that confers upon a male mouse the ability to generate offspring by mating. Mice and cells with genetically modified immunoglobulin heavy chain loci that comprise an ectopic nucleotide sequence encoding a mouse ADAM6 or functional fragment or homolog or ortholog thereof are also provided.

Claims (33)

1. A genetically modified mouse whose genome comprises:

(a) ectopic placement of an ADAM6 gene; and

(b) a human immunoglobulin heavy chain variable region locus comprising an insertion of one or more human V H gene segments, one or more human D H gene segments, and one or more human J H gene segments into the endogenous mouse heavy chain locus, wherein the human V H , D H and J H gene segments are operably linked to a heavy chain constant region gene;

so that the mouse is characterized in that:

(i) it is fertile; and

(ii) when it is immunized with an antigen, it generates antibodies comprising heavy chain variable domains encoded by the one or more human V H , one or more human D H , and one or more human J H gene segments, linked to heavy chain constant domains encoded by the heavy chain constant region gene, wherein the antibodies show specific binding to the antigen.

2. The mouse of claim 1 , wherein the insertion reduces or eliminates Adam6 activity of a cell or tissue of a male mouse.

3. The mouse of claim 1 , wherein the ADAM6 gene is present at the human heavy chain variable region locus.

4. The mouse of claim 1 , wherein the ADAM6 gene is present at a position other than the human heavy chain variable gene locus.

5. The mouse of claim 1 , wherein the ADAM6 gene includes mouse ADAM6a gene and/or mouse ADAM6b gene.

6. The mouse of claim 1 , wherein the one or more human V H gene segments includes at least 18, at least 39, or at least 80 human V H gene segments.

7. The mouse of claim 1 , wherein the human immunoglobulin heavy chain variable region locus comprises at least 18 human V H gene segments, at least one and up to 27 human DH gene segments, and at least one and up to six human J H gene segments.

8. The mouse of claim 1 , wherein the human immunoglobulin heavy chain variable region locus comprises at least 39 human V H gene segments, at least one and up to 27 human DH gene segments and at least one and up to six human J H gene segments.

9. The mouse of claim 1 , wherein the human immunoglobulin heavy chain variable region locus comprises 80 human V H gene segments, at least one and up to 27 human DH gene segments, and at least one and up to six human J H gene segments.

10. The mouse of claim 1 , wherein the constant region gene is a mouse constant region gene.

11. The mouse of claim 10 , wherein the mouse constant region gene comprises a constant region selected from a CH 1 , a hinge, a CH 2 , a CH 3 and/or a CH 4 or a combination thereof.

12. The mouse of claim 1 , further comprising an insertion of one or more human Vκ gene segments and one or more human Jκ gene segments into the endogenous κ light chain locus.

13. The mouse of claim 12 , wherein the one or more human Vκ gene segments and one or more human Jκ gene segments are operably linked to a rodent light chain constant region gene.

14. An isolated mouse cell whose genome comprises:

(a) ectopic placement of an ADAM6 gene; and

(b) a human immunoglobulin heavy chain variable region locus comprising an insertion of one or more human V H gene segments, one or more human D H gene segments, and one or more human J H gene segments into the endogenous heavy chain locus, wherein the human V H , D H and J H gene segments are operably linked to a heavy chain constant region gene.

15. The isolated cell of claim 14 , wherein the cell is an embryonic stem cell.

16. A mouse embryo generated from the embryonic stem cell of claim 15 .

17. The isolated cell of claim 14 , wherein the cell is a B cell.

18. A hybridoma made from the B cell of claim 17 .

19. An immortalized cell made from the isolated cell of claim 14 .

20. A method of providing an antibody specific for an antigen of interest, the method comprising the steps of:

(a) immunizing a mouse of claim 1 with the antigen of interest, which mouse has a genome comprising (a) and (b) of claim 1 ;

(b) isolating at least one B cell from the mouse producing an antibody specific against the antigen; and

(c) culturing at least one cell producing the antibody of step b) and obtaining said produced antibody.

21. The method of claim 20 , wherein step (c) further comprises making a hybridoma employing the cell of step (b) and culturing the hybridoma.

22. The method of claim 20 , wherein the at least one B cell obtained in step (b) is derived from the spleen, a lymph node or bone marrow of the mouse from step (a).

23. The method of claim 20 , wherein immunizing with the antigen of interest in step (a) is carried out with protein, DNA, a combination of DNA and protein, or cells expressing the antigen.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 26, 2019
From: KAROW, MARGARET
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 049592/0420 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 4, 2012
From: MACDONALD, LYNN; STEVENS, SEAN; MURPHY, ANDREW J.
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 028893/0206 →
Continuity (4)
Provisional Application 61595200 · Feb 6, 2012
Provisional Application 61497650 · Jun 16, 2011
Provisional Application 61446895 · Feb 25, 2011
Related Publication 20120322108A1 · Dec 20, 2012