IP Library Granted Patent US 10,000,572
Granted Patent B2
US 10,000,572 · App. 14/908,368 · Granted Jun 19, 2018

Method for inhibiting the immune suppressive function of human T regulatory cells by administering an anti-GARP monoclonal antibody

Inventors: Sophie Lucas (Tervuren, BE); Pierre Coulie (Kraainem, BE); Julia Cuende Villasur (Louvain, BE); Laure Dumoutier (Orbais, BE); Jean-Christophe Renauld (Kraainem, BE)
Assignees: UNIVERSITÉ CATHOLIQUE DE LOUVAIN; LUDWIG INSTITUTE FOR CANCER RESEARCH LTD
C07K16/2875C07K16/28C07K16/30A61K2039/505C07K2317/22C07K2317/24C07K2317/31C07K2317/32C07K2317/41C07K2317/54C07K2317/55C07K2317/565C07K2317/569C07K2317/622C07K2317/624C07K2317/626C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 10,000,572
App. No.
14/908,368
Granted
Jun 19, 2018
Kind
B2
Abstract

The present invention relates to an antibody binding to the transmembrane protein ‘glycoprotein A repetitions predominant’ (GARP) in the presence of TGF-β and uses thereof.

Claims (8)

1. A method for inhibiting the immune suppressive function of human T regulatory cells (Tregs) in a subject with a TGF-β related disorder, comprising administering to a subject in need thereof an effective amount of a monoclonal antibody capable of binding to a conformational epitope of a complex of human Glycoprotein A Repetitions Predominant (hGARP) and TGF-β, said conformational epitope comprising amino acids of hGARP and amino acids of latent TGF-β, wherein the amino acids of hGARP are at least one of amino acids 137 to 139 of hGARP, and wherein the monoclonal antibody inhibits TGF-β activation, thereby inhibiting Treg function in the subject.

2. The method according to claim 1 , wherein the TGF-β related disorder is cancer.

3. The method according to claim 1 , wherein the monoclonal antibody is administered in combination with a treatment for cancer.

4. The method according to claim 1 , wherein the amino acids of hGARP are amino acids 137 to 139 of hGARP.

5. The method according to claim 1 , wherein the monoclonal antibody is a whole antibody.

6. The method according to claim 1 , wherein the monoclonal antibody is a humanized antibody.

7. The method according to claim 3 , wherein antibody is administered in combination with another immunotherapeutic agent.

8. The method of claim 7 , wherein the other immunotherapeutic agent is a tumor vaccine.

Assignments (5)
CHANGE OF NAME Recorded Feb 26, 2018
From: ARGEN-X N.V.
To: ARGENX SE
Reel/Frame 045441/0013 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2018
From: ARGENX SE
To: ARGENX BVBA
Reel/Frame 045441/0032 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 4, 2016
From: SAUNDERS, MICHAEL; VAN DE WONING, SEBASTIAN; DE HAARD, HANS; DE BOECK, GITTE
To: ARGEN-X N.V.
Reel/Frame 038186/0814 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 4, 2016
From: LUCAS, SOPHIE; COULIE, PIERRE
To: UNIVERSITÉ CATHOLIQUE DE LOUVAIN
Reel/Frame 038186/0833 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 4, 2016
From: RENAULD, JEAN-CHRISTOPHE; VILLASUR, JULIA CUENDE; DUMOUTIER, LAURE
To: LUDWIG INSTITUTE FOR CANCER RESEARCH LTD
Reel/Frame 038186/0839 →
Priority Claims (2)
EP 13178958 · Aug 1, 2013 · regional
EP 14167425 · May 7, 2014 · regional
Continuity (2)
Provisional Application 61861008 · Aug 1, 2013
Related Publication 20160272717A1 · Sep 22, 2016
Cited By (2)
US 12,378,297 US 12,473,343