IP Library Granted Patent US 12,433,266
Granted Patent B2
US 12,433,266 · App. 18/110,276 · Granted Oct 7, 2025

Humanized light chain mice

Inventors: Lynn Macdonald (Harrison, NY); Cagan Gurer (Chappaqua, NY); Karolina A. Hosiawa (Yorktown Heights, NY); Sean Stevens (Del Mar, CA); Andrew J. Murphy (Croton-on-Hudson, NY)
Assignee: Regeneron Pharmaceuticals, Inc.
A01K67/0278C07K16/2866C07K16/462C12N9/6489A01K2217/072A01K2217/15A01K2227/105A01K2267/01C12N2800/204C12N2800/30
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Quick Facts
Patent No.
US 12,433,266
App. No.
18/110,276
Granted
Oct 7, 2025
Kind
B2
Abstract

Non-human animals, tissues, cells, and genetic material are provided that comprise a modification of an endogenous non-human heavy chain immunoglobulin sequence and that comprise an ADAM6 activity functional in a mouse, wherein the non-human animals express a human immunoglobulin heavy chain variable domain and a cognate human immunoglobulin λ light chain variable domain.

Claims (26)

1. A method of making a genetically modified mouse embryonic stem(ES) cell, comprising genetically modifying the mouse ES cell so that its genome comprises:

(a) one or more human Vλ gene segments and one or more human Jλ gene segments upstream of a mouse immunoglobulin κ light chain constant region (Cκ),

(b) 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 upstream of a mouse immunoglobulin heavy chain constant region, and

(c) a nucleotide sequence that encodes a mouse ADAM6 protein, wherein the mouse ADAM6 protein is capable of restoring or enhancing fertility in a genetically modified male mouse.

2. The method of claim 1 , wherein the genome of the mouse ES cell comprises non-functional endogenous V L gene segments and/or endogenous J L gene segments.

3. The method of claim 1 , wherein the one or more human Vλ gene segments comprises at least 12 human Vλ gene segments.

4. The method of claim 1 , wherein the one or more human Vλ gene segments comprises at least 28 human Vλ gene segments.

5. The method of claim 1 , wherein the one or more human Vλ gene segments comprises at least 40 human Vλ gene segments.

6. The method of claim 1 , wherein the nucleotide sequence that encodes a mouse ADAM6 protein is positioned between two human V H gene segments.

7. The method of claim 1 , wherein the nucleotide sequence that encodes a mouse ADAM6 protein is positioned between a human V H gene segment and a human D H gene segment.

8. The method of claim 1 , wherein the one or more human Jλ gene segments are selected from the group consisting of Jλ1, Jλ2, Jλ3, Jλ7, and a combination thereof.

9. The method of claim 1 , wherein the one or more human Jλ gene segments comprises at least four human Jλ gene segments.

10. The method of claim 9 , wherein at least four human Jλ gene segments comprise at least Jλ1, Jλ2, Jλ3, and Jλ7.

11. The method of claim 1 , wherein all endogenous mouse Vκ gene segments and endogenous mouse Jκ gene segments are replaced with the one or more human Vλ gene segments and one or more human Jλ gene segments.

12. The method of claim 1 , wherein the mouse ES cell genome further comprises a human Vκ-Jκ intergenic region from a human κ light chain locus, wherein the human Vκ-Jκ intergenic region is contiguous with the one or more human Vλ gene segments and one or more human Jλ gene segments.

13. The method of claim 12 , wherein the human Vκ-Jκ intergenic region is placed between a human Vλ gene segment and a human Jλ gene segment.

14. The method of claim 12 , wherein the human Vκ-Jκ intergenic region comprises SEQ ID NO: 158.

15. The method of claim 1 , wherein the mouse ADAM6 protein is a mouse ADAM6a and/or ADAM6b protein.

16. The method of claim 1 , wherein the one or more human Vλ gene segments comprise Vλ3-1, Vλ4-3, Vλ2-8, Vλ3-9, Vλ3-10, Vλ2-11, Vλ3-12, or a combination thereof.

17. The method of claim 1 , wherein the one or more human Vλ gene segments comprise human Vλ2-14, Vλ3-16, Vλ2-18, Vλ3-19, Vλ3-21, Vλ3-22, Vλ2-23, Vλ3-25, Vλ3-27, or a combination thereof.

18. The method of claim 1 , wherein the one or more human Vλ gene segments comprise human Vλ1-40, Vλ7-43, Vλ1-44, Vλ5-45, Vλ7-46, Vλ1-47, Vλ9-49, Vλ1-51, Vλ5-52, or a combination thereof.

19. The method of claim 1 , wherein at least two λ light chain enhancers are located downstream of both the one or more human Vλ gene segments and the one or more human Jλ gene segments.

20. A genetically modified mouse embryonic stem(ES) cell comprising in its genome:

(a) one or more human Vλ gene segments and one or more human Jλ gene segments upstream of a mouse immunoglobulin κ light chain constant region (Cκ),

(b) 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 upstream of a mouse immunoglobulin heavy chain constant region, and

(c) a nucleotide sequence that encodes a mouse ADAM6 protein, wherein the mouse ADAM6 protein is capable of restoring or enhancing fertility in a genetically modified male mouse.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 22, 2025
From: MACDONALD, LYNN; GURER, CAGAN; HOSIAWA, KAROLINA A.; STEVENS, SEAN; MURPHY, ANDREW J.
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 069961/0625 →
Continuity (5)
Continuation 16729852 · Dec 30, 2019
Continuation 15585023 · May 2, 2017
Division 13716238 · Dec 17, 2012
Provisional Application 61578097 · Dec 20, 2011
Related Publication 20230337646A1 · Oct 26, 2023
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