IP Library › Granted Patent US 11,576,356
Granted Patent B2
US 11,576,356 · App. 16/782,708 · Granted Feb 14, 2023

Genetically modified non-human animals and methods of use thereof

Inventors: Dietmar Herndler-Brandstetter (New Haven, CT); Richard A. Flavell (Guilford, CT); Davor Frleta (Tarrytown, NY); Cagan Gurer (Tarrytown, NY); Markus Gabriel Manz (Zollikon, CH); Andrew J. Murphy (Croton-on-Hudson, NY); Noah W. Palm (New Haven, CT); Liang Shan (New Haven, CT); Sean Stevens (Del Mar, CA); Till Strowig (Braunschweig, DE); George D. Yancopoulos (Yorktown Heights, NY); Marcel de Zoete (Amersfoort, NL)
Assignees: Regeneron Pharmaceuticals, Inc.; Yale University; Institute for Research in Biomedicine (IRB)
A01K67/0278A01K67/0271A61K49/0008A01K2207/12A01K2217/072A01K2217/15A01K2227/105A01K2267/0331A01K2267/0337
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Quick Facts
Patent No.
US 11,576,356
App. No.
16/782,708
Granted
Feb 14, 2023
Kind
B2
Abstract

Genetically modified non-human animals expressing human SIRPα and human IL-15 from the non-human animal genome are provided. Also provided are methods for making non-human animals expressing human SIRPα and human IL-15 from the non-human animal genome, and methods for using non-human animals expressing human SIRPα and human IL-15 from the non-human animal genome. These animals and methods find many uses in the art, including, for example, in modeling human T cell and/or natural killer (NK) cell development and function, in modeling human pathogen infection of human T cells and/or NK cells, and in various in vivo screens.

Claims (28)

1. A genetically modified mouse, comprising:

a null mutation in the mouse SIRPα gene at the mouse SIRPα gene locus and a nucleic acid sequence encoding a human SIRPα protein incorporated into the genome of the genetically modified mouse and operably linked to an endogenous mouse SIRPα gene promoter at the mouse SIRPα gene locus; and

a null mutation in the mouse IL-15 gene at the mouse IL-15 gene locus and a nucleic acid sequence encoding a human IL-15 protein incorporated into the genome of the genetically modified mouse and is operably linked to an endogenous mouse IL-15 gene promoter at the mouse IL-15 gene locus,

wherein the genetically modified mouse expresses the human SIRPα protein and the human IL-15 protein, and

wherein the genetically modified mouse is immunodeficient and comprises a Rag2 gene knock-out and an IL2rg gene knock-out, a Rag2 gene knock-out, or an IL2rg gene knock-out.

2. The genetically modified mouse according to claim 1 , wherein the null mutation is a deletion of at least mouse SIRPα exons 2-4 and wherein the genetically modified mouse is heterozygous for the allele comprising the nucleic acid sequence encoding the human SIRPα protein.

3. The genetically modified mouse according to claim 1 , wherein the null mutation is a deletion of at least mouse SIRPα exons 2-4 and wherein the genetically modified mouse is homozygous for the allele comprising the nucleic acid sequence encoding the human SIRPα protein.

4. The genetically modified mouse according to claim 1 , wherein the human SIRPα protein is a functional fragment of a full length human SIRPα protein.

5. The genetically modified mouse according to claim 4 , wherein the functional fragment comprises an extracellular domain of human SIRPα.

6. The genetically modified mouse according to claim 1 , wherein the human IL-15 protein is a functional fragment of a full-length human IL-15 protein.

7. The genetically modified mouse according to claim 1 , wherein the null mutation is a deletion of at least mouse IL-15 exons 5-8, wherein the genetically modified mouse is heterozygous for the allele comprising the nucleic acid sequence encoding the human IL-15 protein.

8. The genetically modified mouse according to claim 1 , wherein the null mutation is a deletion of at least mouse IL-15 exons 5-8, wherein the genetically modified mouse is homozygous for the allele comprising the nucleic acid sequence that encodes the human IL-15 protein.

9. The genetically modified mouse according to claim 1 , wherein the genetically modified mouse comprises an engraftment of human hematopoietic cells.

10. The genetically modified mouse according to claim 9 , wherein the genetically modified mouse comprises an infection with a human pathogen.

11. The genetically modified mouse according to claim 10 , wherein the human pathogen activates, induces and/or targets T cells.

12. The genetically modified mouse according to claim 10 , wherein the human pathogen activates, induces and/or targets natural killer (NK) cells.

13. The genetically modified mouse according to claim 10 , wherein the human pathogen is a pathogen that infects human intestine or the human lung.

14. An animal engraftment model, comprising a genetically modified mouse comprising:

a null mutation in the mouse SIRPα gene at the mouse SIRPα gene locus and a nucleic acid sequence incorporated into the genome of the genetically modified mouse, which sequence encodes a human SIRPα protein and is operably linked to an endogenous mouse SIRPα gene promoter at the mouse SIRPα gene locus;

a null mutation in the mouse IL-15 gene at the mouse IL-15 gene locus and a nucleic acid sequence incorporated into the genome of the genetically modified mouse, which sequence encodes a human IL-15 protein and is operably linked to an endogenous mouse IL-15 gene promoter at the mouse IL-15 gene locus; and

an engraftment of human hematopoietic cells, wherein the genetically modified mouse (i) expresses the human SIRPα protein and the human IL-15 protein, and (ii) comprises human intraepithelial lymphocytes (IELs) in the lung or small intestine and Peyer's patches of the genetically modified mouse,

wherein the genetically modified mouse is immunodeficient and comprises a Rag2 gene knock-out and an IL2rg gene knock-out, a Rag2 gene knock-out, or an IL2rg gene knock-out.

15. The engraftment model according to claim 14 , wherein the null mutation is a deletion of at least mouse SIRPα exons 2-4, wherein the genetically modified mouse is heterozygous for the allele comprising the nucleic acid sequence that encodes the human SIRPα protein.

16. The engraftment model according to claim 14 , wherein the null mutation is a deletion of at least mouse SIRPα exons 2-4, wherein the genetically modified mouse is homozygous for the allele comprising the nucleic acid sequence that encodes the human SIRPα protein.

17. The engraftment model according to claim 14 , wherein the human SIRPα protein is a functional fragment of a full length human SIRPα protein and the human IL-15 protein is a functional fragment of a full-length human IL-15 protein.

18. The engraftment model according to claim 17 , wherein the functional fragment comprises an extracellular domain of human SIRPα.

19. The engraftment model according to claim 14 , wherein the null mutation is a deletion of at least mouse IL-15 exons 5-8, wherein the genetically modified mouse is heterozygous for the allele comprising the nucleic acid sequence that encodes the human IL-15 protein.

20. The engraftment model according to claim 14 , wherein the null mutation is a deletion of at least mouse IL-15 exons 5-8, wherein the genetically modified mouse is homozygous for the allele comprising the nucleic acid sequence that encodes the human IL-15 protein.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 12, 2020
From: HERNDLER-BRANDSTETTER, DIETMAR; SHAN, LIANG; DE ZOETE, MARCEL; PALM, NOAH W.; FLAVELL, RICHARD A.; STROWIG, TILL
To: YALE UNIVERSITY
Reel/Frame 052098/0130 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 12, 2020
From: FRLETA, DAVOR; GURER, CAGAN; MURPHY, ANDREW J.; STEVENS, SEAN; YANCOPOULOS, GEORGE D.
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 052098/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 12, 2020
From: MANZ, MARKUS GABRIEL
To: INSTITUTE FOR RESEARCH IN BIOMEDICINE (IRB)
Reel/Frame 052097/0832 →
Continuity (6)
Continuation 15954450 · Apr 16, 2018
Continuation 15097239 · Apr 12, 2016
Provisional Application 62146938 · Apr 13, 2015
Provisional Application 62148667 · Apr 16, 2015
Provisional Application 62287842 · Jan 27, 2016
Related Publication 20200229410A1 · Jul 23, 2020