Therapeutic trem-1 peptides

US2016193288A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016193288-A1
Application numberUS-201514968479-A
CountryUS
Kind codeA1
Filing dateDec 14, 2015
Priority dateNov 29, 2004
Publication dateJul 7, 2016
Grant date

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

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

First claim

Opening claim text (preview).

1 .- 40 . (canceled) 41 . An isolated peptide or a derivative thereof, which is capable of acting as antagonist of the TREM-1 protein as defined by SEQ ID NO.2, comprising SEQ ID NO. 22 or at least 3 amino acids from SEQ ID NO. 23, wherein: (a) the polypeptide consists of: (i) a contiguous sequence of 5 to 29 amino acids from SEQ ID NO: 2; or (ii) a contiguous sequence of 5 to 29 amino acids from SEQ ID NO: 2 in which one amino acid is substituted conservatively with another amino acid; or (b) the polypeptide consists of an amino acid sequence having at least 80% sequence identity to SEQ ID NOS: 3, 4, 6 or 7; wherein the derivatives of the polypeptides of (a) or (b) are modified by glycosylation, acetylation, pegylation, phosphorylation, amidation, or derivatization by protecting or blocking groups. 42 . The isolated peptide or derivative thereof according to claim 41 which consists of: (a) a contiguous sequence of 5 to 29 amino acids from SEQ ID NO: 2; or (b) a contiguous sequence of 5 to 29 amino acids from SEQ ID NO: 2 in which one amino acid is substituted conservatively with another amino acid; and wherein the derivatives of the polypeptides of (a) or (b) are modified by glycosylation, acetylation, pegylation, phosphorylation, amidation, or derivatization by protecting or blocking groups. 43 . The isolated peptide or derivative thereof according to claim 41 wherein the polypeptide consists of an amino acid sequence having at least 80% sequence identity to SEQ ID NOS: 3, 4, 6 or 7; and wherein the derivatives of the polypeptide are modified by glycosylation, acetylation, pegylation, phosphorylation, amidation, or derivatization by protecting or blocking groups. 44 . The isolated peptide or derivative thereof according to claim 41 , wherein said polypeptide consists of a contiguous sequence of 15 to 29 amino acids from SEQ ID NO.2. 45 . The isolated peptide or derivative thereof according to claim 41 which comprises at least 3 amino acids from SEQ ID NO. 23 wherein the at least 3 amino acids from SEQ ID NO. 23 are selected from the group consisting of HPP, HPPN (SEQ ID NO 25), and HPPND (SEQ ID NO 23). 46 . A polypeptide that is a fusion protein comprising the isolated peptide or derivative thereof according to claim 41 and a heterologous polypeptide. 47 . A polypeptide according to claim 46 wherein the heterologous polypeptide is selected from the group consisting of: a sequence derived from an immunoglobulin, a non-classical alternative protein scaffold a heterologous signal sequence fused to the N-terminus of the peptide according to claim 41 or derivative thereof, and a tag sequence. 48 . A pharmaceutical composition comprising a peptide or derivative thereof according to claim 41 and a pharmaceutically acceptable carrier.

Assignees

Inventors

Classifications

  • Immunoglobulin superfamily · CPC title

  • A61K38/177Primary

    Receptors; Cell surface antigens; Cell surface determinants · CPC title

  • Immunomodulators · CPC title

  • Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title

  • containing domain for protein-protein interaction · CPC title

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What does patent US2016193288A1 cover?
A polypeptide comprising one or more sequences derived from CDR2 or CDR3 of a TREM-1 protein, characterised by the ability to treat, ameliorate, or lessen the symptoms of conditions including sepsis, septic shock or sepsis-like conditions and IBD.
Who is the assignee on this patent?
Bristol Myers Squibb Co, Univ Lorraine
What technology area does this patent fall under?
Primary CPC classification C07K14/70503. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jul 07 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).