IP Library Granted Patent US 8,822,169
Granted Patent B2
US 8,822,169 · App. 13/402,057 · Granted Sep 2, 2014

HMG1 antibody for treating inflammatory conditions

Inventors: Kevin J. Tracey (Old Greenwich, CT); Haichao Wang (Avenel, NJ)
Assignee: The Feinstein Institute for Medical Research
A61K39/395C07K2316/96G01N2800/245A61K2039/505G01N33/6875G01N2800/26G01N2800/125G01N2800/067C07K16/24G01N2800/065
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Quick Facts
Patent No.
US 8,822,169
App. No.
13/402,057
Granted
Sep 2, 2014
Kind
B2
Abstract

There is disclosed a pharmaceutical composition and method for treating sepsis, including septic shock and ARDS (acute respiratory distress syndrome), comprising administering an effective amount of a HMG1 antagonist. There is further disclosed a diagnostic method for monitoring the severity or potential lethality of sepsis or septic shock, comprising measuring the serum concentration of HMG1 in a patient exhibiting or at risk of exhibiting sepsis or septic shock symptoms. Lastly, there is disclosed a pharmaceutical composition and method for effecting weight loss or treating obesity, comprising administering an effective amount of HMG1 or a therapeutically active HMG1 fragment.

Claims (6)

1. A pharmaceutical composition comprising an effective amount of an antagonist of high mobility group 1 (HMG1) protein, wherein the amount of the antagonist is effective to inhibit HMG1-mediated activation of the inflammatory cytokine cascade, and wherein the HMG1 antagonist is selected from an antibody that specifically binds to HMG1, an antigen-binding fragment of said antibody, or an HMG1 antisense sequence, wherein the HMG1 comprises an antigenic fragment of SEQ ID NO: 4.

2. The composition of claim 1 , which is in the form of a tablet, pill, capsule, liquid, gel, syrup, slurry, suspension, skin patch, topical cream, mucosal patch, mucosal liquid, mucosal gel, or is suitable for administration to the respiratory tract by inhaler.

3. The composition of claim 1 , further comprising a solid excipient selected from a sugar, a cellulose preparation, a gelatin, a gum, polyvinylpyrrolidone, or a combination thereof.

4. The composition of claim 1 , further comprising a disintegrating agent and/or stabilizer.

5. A method of treating a TNF-mediated, IL-1-mediated, or lipopolysaccharide (LPS)-mediated activation of the inflammatory cytokine cascade, comprising administering an effective amount of the composition of claim 1 .

6. The method of claim 5 , wherein the HMG1 antagonist is an antibody or antigen-binding fragment thereof that inhibits HMG-1-mediated activation of the inflammatory cytokine cascade.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 27, 2012
From: TRACEY, KEVIN J.; WANG, HAICHAO
To: NORTH SHORE-LONG ISLAND JEWISH RESEARCH INSTITUTE
Reel/Frame 028653/0992 →
CHANGE OF NAME Recorded Jul 27, 2012
From: NORTH SHORE-LONG ISLAND JEWISH RESEARCH INSTITUTE
To: THE FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH
Reel/Frame 028656/0655 →
Continuity (6)
Continuation 12496333 · Jul 1, 2009
Division 11477835 · Jun 29, 2006
Continuation 10210747 · Jul 31, 2002
Continuation 09503632 · Feb 14, 2000
Division 09248574 · Feb 11, 1999
Related Publication 20130028910A1 · Jan 31, 2013