Therapeutic TREM-1 peptides

US10603357B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10603357-B2
Application numberUS-201514968479-A
CountryUS
Kind codeB2
Filing dateDec 14, 2015
Priority dateNov 29, 2004
Publication dateMar 31, 2020
Grant dateMar 31, 2020

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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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).

The invention claimed is: 1. An isolated polynucleotide comprising a nucleotide sequence, which encodes a peptide which is capable of acting as antagonist of the TREM-1 protein as defined by SEQ ID NO: 2 and one or more expression control elements that control expression of the peptide; wherein the peptide comprises SEQ ID NO: 22 or at least 3 amino acids from SEQ ID NO: 23; and wherein the peptide 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. 2. A vector comprising the polynucleotide of claim 1 . 3. An isolated polynucleotide comprising a nucleotide sequence, which encodes a peptide consisting of SEQ ID NO: 19 or SEQ ID NO: 7 and a heterologous signal sequence. 4. A vector comprising the isolated polynucleotide of claim 2 . 5. An isolated polynucleotide comprising a nucleotide sequence encoding a peptide and one or more expression control elements that control expression of the peptide; wherein the peptide is capable of acting as an antagonist of the TREM-1 protein as defined by SEQ ID NO: 1; wherein the peptide comprises the amino acid sequence of SEQ ID NO: 20 or at least 3 amino acids of SEQ ID NO: 21; and wherein 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. 6. A vector comprising the polynucleotide of claim 5 . 7. The polynucleotide of claim 5 , wherein the peptide consists of an amino acid sequence having the sequence of SEQ ID NOs: 16, 17, 18 or 19. 8. The polynucleotide of claim 7 , wherein the peptide consists of an amino acid sequence having the sequence of SEQ ID NO: 19. 9. The polynucleotide of claim 5 , 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 the sequence of SEQ ID NO: 16, 17, 18, or 19 by one or more conservative amino acid modifications. 10. The polynucleotide of claim 9 , wherein the peptide consists of an amino acid sequence having the sequence of SEQ ID NO: 19, or which differs from the sequence of SEQ ID NO: 19 by one or more conservative amino acid modifications. 11. The polynucleotide of claim 5 , wherein the peptide consists of a contiguous sequence of 5 to 29 amino acids from SEQ ID NO: 1. 12. The polynucleotide of claim 5 , wherein the peptide 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). 13. The vector of claim 6 , wherein the expression control element comprises a promoter, an enhancer, a transcription terminator, or a polyadenylation site. 14. A host cell comprising the polynucleotide of claim 5 . 15. The host cell of claim 14 , which is a prokaryotic cell. 16. The host cell of claim 14 , which is a eukaryotic cell. 17. A method of expressing a peptide in a host cell comprising transforming the host cell with the polynucleotide of claim 5 in a culture medium. 18. The method of claim 17 , further comprising purifying the expressed peptide.

Assignees

Inventors

Classifications

  • Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics · CPC title

  • of vertebrates · CPC title

  • Drugs for disorders of the blood or the extracellular fluid · CPC title

  • Immunomodulators · CPC title

  • Bowel diseases, e.g. Crohn, ulcerative colitis, IBS · CPC title

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What does patent US10603357B2 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?
Univ De Lorraine, Bristol Myers Squibb Co
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 Tue Mar 31 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). 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).