IP Library Granted Patent US 10,426,848
Granted Patent B2
US 10,426,848 · App. 15/601,363 · Granted Oct 1, 2019

Humanized FcγR mice

Inventors: Lynn MacDonald (Harrison, NY); Naxin Tu (Pleasantville, NY); Cagan Gurer (Chappaqua, NY); Sean Stevens (Del Mar, CA); Andrew J. Murphy (Croton-On-Hudson, NY)
Assignee: Regeneron Pharmaceuticals, Inc.
A61K49/0008A01K67/0276A01K67/0278C07K14/70535G01N33/5014A01K2207/15A01K2217/072A01K2217/075A01K2217/15A01K2227/105A01K2267/03A01K2267/0387
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,426,848
App. No.
15/601,363
Granted
Oct 1, 2019
Kind
B2
Abstract

Genetically modified non-human animals and methods and compositions for making and using them are provided, wherein the genetic modification comprises a deletion of the endogenous low affinity FcγR locus, and wherein the mouse is capable of expressing a functional FcRγ-chain. Genetically modified mice are described, including mice that express low affinity human FcγR genes from the endogenous FcγR locus, and wherein the mice comprise a functional FcRγ-chain. Genetically modified mice that express up to five low affinity human FcγR genes on accessory cells of the host immune system are provided.

Claims (18)

1. A genetically modified mouse whose genome comprises at least one human low affinity FcγR α-chain gene encoding a human low affinity FcγR α-chain with a polymorphism, wherein the human low affinity FcγR α-chain gene replaces an endogenous low affinity FcγR α-chain gene, and wherein the mouse comprises a functional endogenous FcR γ-chain and functionally expresses the human low affinity FcγR α-chain gene.

2. The genetically modified mouse of claim 1 , wherein the human low affinity FcγR α-chain is a low affinity FcγRIIA α-chain.

3. The genetically modified mouse of claim 2 , wherein the polymorphism is a 131His polymorphism.

4. The genetically modified mouse of claim 2 , wherein the polymorphism is a 131Arg polymorphism.

5. The genetically modified mouse of claim 1 , wherein the human low affinity FcγR α-chain is a low affinity FcγRIIB α-chain.

6. The genetically modified mouse of claim 5 , wherein the polymorphism is a 232Ile polymorphism.

7. The genetically modified mouse of claim 5 , wherein the polymorphism is a 232Thr polymorphism.

8. The genetically modified mouse of claim 1 , wherein the human low affinity FcγR α-chain is a low affinity FcγRIIIA α-chain.

9. The genetically modified mouse of claim 8 , wherein the polymorphism is a 158Val polymorphism.

10. The genetically modified mouse of claim 8 , wherein the polymorphism is a 158Phe polymorphism.

11. A method of making a genetically modified mouse whose genome comprises a replacement of the endogenous low affinity FcγR α-chain genes with at least two human low affinity FcγR α-chain genes encoding human low affinity FcγR α-chains, the method comprising:

replacing the endogenous low affinity FcγR α-chain genes with at least two human low affinity FcγR α-chain genes encoding human low affinity FcγR α-chains,

such that the mouse comprises a functional FcR γ-chain and functionally expresses the at least two human FcγR α-chain genes.

12. The method of claim 11 , wherein the functional FcR γ-chain is an endogenous FcR γ-chain.

13. The method of claim 11 , wherein the at least two human low affinity FcγR α chain genes are selected from a human low affinity FcγRIIA, FcγRIIB, FcγRIIC, FcγRIIIA, or FcγRIIIB α chain gene.

14. The method of claim 11 , wherein the at least two human low affinity FcγR a chain genes are human low affinity FcγRIIA and FcγRIIIA α chain genes.

15. A method of making a mouse whose genome comprises a replacement of an endogenous low affinity FcγR α-chain gene with a human low affinity FcγR α-chain gene encoding a human low affinity FcγR α-chain comprising a polymorphism, the method comprising replacing an endogenous low affinity FcγR α-chain gene with a human low affinity FcγR α-chain gene encoding a human low affinity FcγR α-chain gene comprising a polymorphism, wherein the mouse further comprises a functional endogenous FcR γ-chain.

16. The method of claim 15 , wherein the human low affinity FcγR α-chain comprising a polymorphism is selected from the group consisting of a low affinity FcγRIIA α-chain comprising a 131His polymorphism, a low affinity FcγRIIA α-chain comprising a 131Arg polymorphism, a low affinity FcγRIIB α-chain comprising a 232Ile polymorphism, a low affinity FcγRIIB α-chain comprising a 232Thr polymorphism, a low affinity FcγRIIIA α-chain comprising a 158Val polymorphism, and a low affinity FcγRIIB α-chain comprising a 158Phe polymorphism.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 12, 2017
From: MACDONALD, LYNN; TU, NAXIN; GURER, CAGAN; STEVENS, SEAN; MURPHY, ANDREW J.
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 042988/0472 →
Continuity (6)
Continuation 14800253 · Jul 15, 2015
Continuation 14152106 · Jan 10, 2014
Division 13466225 · May 8, 2012
Continuation 12971080 · Dec 17, 2010
Provisional Application 61288562 · Dec 21, 2009
Related Publication 20180015185A1 · Jan 18, 2018