IP Library Granted Patent US 8,329,186
Granted Patent B2
US 8,329,186 · App. 12/611,090 · Granted Dec 11, 2012

Treatment of inflammation using BST2 inhibitor

Assignee: Isu Abxis Co., Ltd
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Quick Facts
Patent No.
US 8,329,186
App. No.
12/611,090
Granted
Dec 11, 2012
Kind
B2
Abstract

The application discloses a method of preventing immune cells from binding to other cells, which includes contacting the immune cells and the other cells with a composition comprising Bst2 antagonist.

Claims (9)

1. A method of reducing inflammation in a subject suffering from sepsis comprising administering a composition comprising a bone marrow stromal cell antigen 2 (Bst2) antagonist to a site of the inflammation, wherein said Bst2 antagonist comprises a soluble portion of Bst2, which comprises an extracellular portion of Bst2 or a fragment of the extracellular portion, in an amount effective to inhibit binding between a first leukocyte and a second leukocyte or an endothelial cell, wherein the extracellular portion is shown in amino acid positions 44 to 180 of SEQ ID NO:73.

2. The method according to claim 1 , wherein the Bst2 antagonist is a Fc chimeric or fusion construct, an albumin chimeric or fusion construct, or linked to a non-proteinaceous polymer.

3. A method of treating sepsis in a subject comprising administering a composition comprising a bone marrow stromal cell antigen 2 (Bst2) antagonist to the person in need thereof, wherein said Bst2 antagonist comprises a soluble portion of Bst2, which comprises an extracellular portion of Bst2 or a fragment of the extracellular portion, in an amount effective to inhibit binding between a first leukocyte and a second leukocyte or an endothelial cell, wherein the extracellular portion is shown in amino acid positions 44 to 180 of SEQ ID NO:73.

4. The method according to claim 1 , wherein the extracellular portion is shown in amino acid positions 44 to 159 of SEQ ID NO:73.

5. The method according to claim 1 , wherein said first leukocyte and the second leukocyte or the endothelial cell are located either at a site of inflammation or at a site distant from inflammation but can transmit inflammatory and immune cytokines or other inflammatory signals to a site of inflammation.

6. The method according to claim 3 , wherein the extracellular portion is shown in amino acid positions 44 to 159 of SEQ ID NO:73.

7. The method according to claim 3 , wherein the Bst2 antagonist is a Fc chimeric or fusion construct, an albumin chimeric or fusion construct, or linked to a non-proteinaceous polymer.

8. The method according to claim 3 , wherein said first leukocyte and the second leukocyte or the endothelial cell are located either at a site of inflammation or at a site distant from inflammation but can transmit inflammatory and immune cytokines or other inflammatory signals to a site of inflammation.

9. A method of inhibiting systemic inflammation in a subject suffering from sepsis comprising administering a composition comprising a bone marrow stromal cell antigen 2 (Bst2) antagonist to a site of the inflammation, wherein said Bst2 antagonist comprises a soluble portion of Bst2, which comprises an extracellular portion of Bst2 or a fragment of the extracellular portion, in an amount effective to inhibit binding between a first leukocyte and a second leukocyte or an endothelial cell, wherein the extracellular portion is shown in amino acid positions 44 to 180 of SEQ ID NO:73.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 2, 2009
From: KIM, MYUNG; CHUNG, JAY; PARK, JUNE-YOUNG; YOO, HYOUNGA; LEE, SANG-MIN; LEE, YOON-SEOK; KOO, MISON; PARK, SANG-HO
To: ISU ABXIS CO., LTD
Reel/Frame 023459/0025 →
Priority Claims (1)
KR 10-2004-0108909 · Dec 20, 2004 · national
Continuity (4)
Continuation In Part 11757329 · Jun 1, 2007
Continuation In Part 11471853 · Jun 20, 2006
Continuation In Part PCTKR2005004398 · Dec 20, 2005
Related Publication 20100129365A1 · May 27, 2010