IP Library Granted Patent US 9,273,111
Granted Patent B2
US 9,273,111 · App. 13/181,323 · Granted Mar 1, 2016

Therapeutic TREM-1 peptides

Inventors: Gilbert Faure (Vandoeuvre les Nancy, FR); Sebastien Gibot (Vandoeuvre les Nancy, FR); Paola Panina (Milan, IT); Nadia Passini (Milan, IT)
Assignees: Universite de Lorraine; Bristol-Myers Squibb
C07K14/705G01N33/5088A61K38/00G01N2800/065G01N2800/26
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Quick Facts
Patent No.
US 9,273,111
App. No.
13/181,323
Granted
Mar 1, 2016
Kind
B2
Abstract

A polypeptide comprising one or more sequences derived from CDR2 or CDR3 of a TREM-1 protein, characterized by the ability to treat, ameliorate, or lessen the symptoms of conditions including sepsis, septic shock or sepsis-like conditions and IBD.

Claims (19)

1. An isolated peptide or derivative thereof, which is capable of acting as an antagonist of the TREM-1 protein as defined by SEQ ID NO. 1, comprising the amino acid sequence of SEQ ID NO. 20 or at least 3 amino acids of SEQ ID NO. 21, wherein:

(a) the peptide consists of:

(i) a contiguous sequence of 5 to 29 amino acids from SEQ ID NO: 1; or

(ii) a contiguous sequence of 5 to 29 amino acids from SEQ ID NO: 1 in which one amino acid is substituted conservatively with another amino acid; or

(b) the peptide consists of an amino acid sequence having at least 80% sequence identity to SEQ ID NOs: 16, 17, 18 or 19; and

wherein the derivatives of the peptides of (a) or (b) are modified by glycosylation, acetylation, pegylation, phosphorylation, amidation, or derivatization by protecting or blocking groups.

2. The isolated peptide or derivative thereof according to claim 1 , which consists of:

(a) a contiguous sequence of 5 to 29 amino acids from SEQ ID NO: 1; or

(b) a contiguous sequence of 5 to 29 amino acids from SEQ ID NO: 1 in which one amino acid is substituted conservatively with another amino acid; and

wherein the derivatives of the peptides of (a) or (b) are modified by glycosylation, acetylation, pegylation, phosphorylation, amidation, or derivatization by protecting or blocking groups.

3. The isolated peptide or derivative thereof according to claim 1 , wherein the peptide consists of an amino acid sequence having at least 80% sequence identity to SEQ ID NOs: 16, 17, 18 or 19;

and wherein the derivatives of the peptide are modified by glycosylation, acetylation, pegylation, phosphorylation, amidation, or derivatization by protecting or blocking groups.

4. The isolated peptide or a derivative thereof according to claim 3 , wherein the peptide consists of an amino acid sequence having at least 80% sequence identity to SEQ ID NO: 19.

5. The isolated peptide or derivative thereof according to claim 3 , wherein the peptide consists of an amino acid sequence having the sequence of SEQ ID NOs: 16, 17, 18 or 19, or which differs from said sequence by one or more conservative amino acid modifications.

6. The isolated peptide according to claim 4 , wherein the peptide consists of an amino acid having the sequence of SEQ ID NO: 19, or which differs from said sequence by one or more conservative modifications.

7. The isolated peptide or derivative thereof according to claim 1 , wherein said peptide consists of a contiguous sequence of 15 to 29 amino acids from SEQ ID NO. 1.

8. The isolated peptide or derivative thereof according to claim 1 , which comprises at least 3 amino acids from SEQ ID NO. 21, wherein the at least 3 amino acids from SEQ ID NO. 21 are selected from the group consisting of QPP, QPPK (SEQ ID NO: 24), and QPPKE (SEQ ID NO. 21).

9. The isolated peptide or derivative thereof according to claim 3 , wherein the peptide consists of an amino acid sequence having the sequence of SEQ ID NOs: 16, 17, 18 or 19.

10. A composition comprising the isolated peptide or derivative thereof according to claim 1 , and a pharmaceutically acceptable carrier.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 30, 2017
From: FAURE, GILBERT; GIBOT, SEBASTEIN; PANINA, PAOLA; PASSINI, NADIA
To: BIOXELL S.P.A.; UNIVERSITE HENRI POINCARE - NANCY I
Reel/Frame 043982/0920 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 30, 2017
From: BIOXELL S.P.A.
To: NOVO NORDISK A/S
Reel/Frame 043982/0948 →
MERGER Recorded Mar 15, 2016
From: UNIVERSITE DE NANCY 1 HENRI POINCARE
To: UNIVERSITE DE LORRAINE
Reel/Frame 038087/0173 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 24, 2015
From: NOVO NORDISK A/S
To: BRISTOL-MYERS SQUIBB COMPANY
Reel/Frame 037133/0836 →
MERGER Recorded Nov 24, 2015
From: UNIVERSITE HENRI POINCARE - NANCY I
To: UNIVERSITE DE LORRAINE
Reel/Frame 037157/0053 →
Priority Claims (2)
GB 0426146.7 · Nov 29, 2004 · national
JP 2005-146848 · May 19, 2005 · national
Continuity (3)
Continuation 12320707 · Feb 2, 2009
Continuation In Part 11284086 · Nov 22, 2005
Related Publication 20120015867A1 · Jan 19, 2012