IP Library Granted Patent US 10,660,317
Granted Patent B2
US 10,660,317 · App. 15/348,162 · Granted May 26, 2020

Genetically modified non-human mammals and cells

Inventors: Teizo Fujita (Fukushima, JP); Hans-Wilhelm Schwaeble (Mountsorrel, GB); Cordula Margaret Stover (Wigston Meadows, GB)
Assignee: University of Leicester
A01K67/0278A01K67/0276C07K16/2851C07K16/40C12N9/6424C12N15/8509A01K2207/15A01K2217/00A01K2217/072A01K2217/075A01K2227/105A01K2267/01A01K2267/03A61K38/00C07K2317/14C12N2510/00C12N2517/00C12N2800/30
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 10,660,317
App. No.
15/348,162
Granted
May 26, 2020
Kind
B2
Abstract

Genetically modified mammals are described which lack the mannan binding lectin associated serine protease MASP-2, together with methods and constructs for their production. Such mammals are useful as models for disorders of the complement system, and in the identification of treatments for such disorders. Also described are mammals which lack the associated protein MAp19; such mammals may also lack MASP-2.

Claims (5)

1. A method for production of an antibody directed against a human MASP-2 protein, the method comprising the step of introducing a human MASP-2 protein, or an immunogenic portion thereof, into a genetically modified mouse, wherein

(i) the genetically modified mouse is homozygous for a null mutation that disrupts exons 10, 11 and 12 of the endogenous MASP-2 gene, wherein the endogenous MASP-2 polypeptide is not produced; or

(ii) the genetically modified mouse is homozygous for a null mutation that disrupts exons 5, 10, 11 and 12 of the endogenous MASP-2 gene, wherein the endogenous MAS-2 polypeptide and the endogenous Map 19 polypeptide are not produced;

and wherein the genetically modified mouse lacks a lectin complement pathway response and retains a classical complement pathway response.

2. The method of claim 1 , wherein all the endogenous MASP-2 gene sequences are absent from the genome of the genetically modified mouse.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Nov 25, 2025
From: WILMINGTON SAVINGS FUND SOCIETY, FSB
To: OMEROS CORPORATION
Reel/Frame 073705/0970 →
CORRECTIVE ASSIGNMENT TO CORRECT THE CORRECT THE BOX TITLED"THIS DOCUMENT SERVES AS AN OATH/DECLARATION (37 CFR 1.63)" WAS ERRONEOUSLY CHECKED AND THIS BOX SHOULD NOT HAVE BEEN CHECKED, PREVIOUSLY RECORDED AT REEL: 67607 FRAME: 108. ASSIGNOR(S) HEREBY CONFIRMS THE SECURITY INTEREST. Recorded Dec 11, 2024
From: OMEROS CORPORATION
To: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS COLLATERAL AGENT
Reel/Frame 069715/0719 →
SECURITY INTEREST Recorded Jun 3, 2024
From: OMEROS CORPORATION
To: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS COLLATERAL AGENT
Reel/Frame 067607/0108 →
RELEASE OF SECURITY INTEREST Recorded Nov 15, 2018
From: CRG SERVICING LLC
To: OMEROS CORPORATION
Reel/Frame 047573/0577 →
SECURITY INTEREST Recorded Jul 3, 2018
From: OMEROS CORPORATION
To: CRG SERVICING LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 046491/0017 →