IP Library Granted Patent US 8,501,173
Granted Patent B2
US 8,501,173 · App. 13/004,415 · Granted Aug 6, 2013

Antibodies to high mobility group-1(HMGB1) B-box polypeptides

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Quick Facts
Patent No.
US 8,501,173
App. No.
13/004,415
Granted
Aug 6, 2013
Kind
B2
Abstract

Compositions and methods are disclosed for inhibiting the release of a proinflammatory cytokine from a vertebrate cell, and for inhibiting an inflammatory cytokine cascade in a patient. The compositions comprise a vertebrate HMGB A box, and an antibody preparation that specifically binds to a vertebrate HMGB B box. The methods comprise treating a cell or a patient with sufficient amounts of the composition to inhibit the release of the proinflammatory cytokine, or to inhibit the inflammatory cytokine cascade.

Claims (10)

1. An isolated antibody or antigen-binding fragment thereof that specifically binds to a B-box fragment of high mobility group B 1 (HMGB1) wherein the B-box fragment: (i) stimulates release of a proinflammatory cytokine selected from the group consisting of TNF, IL-1β, IL-6 and a combination thereof, from a vertebrate cell selected from the group consisting of a macrophage, a monocyte, a neutrophil and a combination thereof and (ii) consists of the amino acid sequence selected from the group consisting of SEQ ID NO:16, SEQ ID NO:23, a fragment of SEQ ID NO: 16, and a fragment of SEQ ID NO: 23, wherein the antibody or antigen-binding fragment inhibits HMGB1-mediated release of a proinflammatory cytokine selected from the group consisting of TNF, IL-1β, IL-6 and a combination thereof from a vertebrate cell selected from the group consisting of a macrophage, a monocyte, a neutrophil and a combination thereof.

2. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-biding fragment thereof is a monoclonal antibody or antigen-binding fragment thereof.

3. The antibody or antigen-binding fragment of claim 1 , wherein the antibody or antigen-binding fragment thereof is a humanized antibody or antigen-binding fragment thereof.

4. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment is a human antibody or antigen-binding fragment thereof.

5. The antibody or antigen-binding fragment of claim 1 , wherein the antibody or antigen-binding fragment thereof is a human monoclonal antibody or an antigen-binding fragment thereof, or a humanized monoclonal antibody or an antigen-binding fragment thereof.

6. The antibody of claim 1 wherein the antibody or antigen-binding fragment thereof is selected from the group consisting of a chimeric antibody, a single chain antibody and an Fab antibody fragment.

7. A composition comprising the antibody of claim 1 and a pharmaceutically acceptable excipient.

8. The composition of claim 7 , further comprising an antagonist of an early sepsis mediator, wherein the antagonist of an early sepsis mediator is an antibody to TNF or MIF, or an IL-1 receptor antagonist.

9. An isolated monoclonal antibody or antigen-binding fragment thereof that specifically binds to a B-box fragment of high mobility group B 1 (HMGB1) wherein the B-box fragment: (i) stimulates release of a proinflammatory cytokine selected from the group consisting of TNF, IL-1β, IL-6 and a combination thereof from a vertebrate cell selected from the group consisting of a macrophage, a monocyte, a neutrophil and a combination thereof, and (ii) consists of the amino acid sequence selected from the group consisting of SEQ ID NO:16, SEQ ID NO:23, a fragment of SEQ ID NO: 16, and a fragment of SEQ ID NO: 23, wherein the antibody or antigen-binding fragment inhibits HMGB1-mediated release of a proinflammatory cytokine selected from the group consisting of TNF, IL-1β, IL-6 and a combination thereof from a vertebrate cell selected from the group consisting of a macrophage, a monocyte, a neutrophil and a combination thereof.

10. An isolated antibody or antigen-binding fragment thereof that specifically binds to a polypeptide consisting of the amino acid sequence selected from the group consisting of SEQ ID NO:16 and SEQ ID NO:23.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 1, 2011
From: FINK, MITCHELL P.
To: UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
Reel/Frame 026842/0011 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 1, 2011
From: TRACEY, KEVIN J.; YANG, HUAN
To: NORTH SHORE-LONG ISLAND JEWISH RESEARCH INSTITUTE
Reel/Frame 026842/0025 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 1, 2011
From: WARREN, HOWLAND SHAW, JR.
To: THE GENERAL HOSPITAL CORPORATION
Reel/Frame 026842/0051 →
CHANGE OF NAME Recorded Sep 1, 2011
From: NORTH SHORE-LONG ISLAND JEWISH RESEARCH INSTITUTE
To: THE FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH
Reel/Frame 026843/0694 →
CONFIRMATORY LICENSE Recorded Apr 5, 2011
From: FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 026075/0462 →
CONFIRMATORY LICENSE Recorded Mar 2, 2011
From: UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025883/0108 →