Neutralizing Antibodies to Nipah and Hendra Virus

US2016272697A2 · US · A2

Patent metadata
FieldValue
Publication numberUS-2016272697-A2
Application numberUS-201214114465-A
CountryUS
Kind codeA2
Filing dateApr 30, 2012
Priority dateApr 28, 2011
Publication dateSep 22, 2016
Grant date

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The invention described herein provides novel peptides. The novel peptides are useful alone or as portions of larger molecules, such as antibodies or antibody fragments, that can be used to treat or prevent infection of Nipah virus and/or Hendra virus.

First claim

Opening claim text (preview).

What is claimed is: 1 . A peptide selected from the group consisting of: a) a peptide comprising an amino acid sequence at least 78% identical to the amino acid sequence of SEQ ID NO: 2, b) a peptide comprising an amino acid sequence at least 82% identical to the amino acid sequence of SEQ ID NO: 2, c) a peptide comprising an amino acid sequence at least 86% identical to the amino acid sequence of SEQ ID NO: 2, d) a peptide comprising an amino acid sequence at least 91% identical to the amino acid sequence of SEQ ID NO: 2, e) a peptide comprising an amino acid sequence at least 95% identical to the amino acid sequence of SEQ ID NO: 2, and f) a peptide comprising an amino acid sequence that is 100% identical to the amino acid sequence of SEQ ID NO: 2, wherein the peptide does not comprise the amino acid sequence of SEQ ID NO: 1. 2 . The peptide of claim 1 , wherein the peptide comprises an amino acid sequence selected from the group consisting of the amino acid sequence of SEQ ID NO: 3, the amino acid sequence of SEQ ID NO: 4, the amino acid sequence of SEQ ID NO: 5, the amino acid sequence of SEQ ID NO: 6, the amino acid sequence of SEQ ID NO: 7, the amino acid sequence of SEQ ID NO: 8, the amino acid sequence of SEQ ID NO: 9, the amino acid sequence of SEQ ID NO: 10, the amino acid sequence of SEQ ID NO: 11, the amino acid sequence of SEQ ID NO: 12, the amino acid sequence of SEQ ID NO: 13, the amino acid sequence of SEQ ID NO: 14, the amino acid sequence of SEQ ID NO: 15, the amino acid sequence of SEQ ID NO: 16, the amino acid sequence of SEQ ID NO: 17, the amino acid sequence of SEQ ID NO: 18, the amino acid sequence of SEQ ID NO: 19, the amino acid sequence of SEQ ID NO: 20, the amino acid sequence of SEQ ID NO: 21, the amino acid sequence of SEQ ID NO: 22, and the amino acid sequence of SEQ ID NO: 23. 3 . An antibody or antibody fragment comprising the peptide of claim 1 , wherein the peptide is a heavy chain complementarity determining region (CDR). 4 . The antibody or antibody fragment of claim 3 , further comprising at least one additional heavy chain CDR. 5 . The antibody or antibody fragment of claim 4 , wherein the at least one additional heavy chain CDR comprises the amino acid sequence of SEQ ID NO: 25. 6 . The antibody or antibody fragment of claim 5 , further comprising a second additional heavy chain CDRs. 7 . The antibody or antibody fragment of claim 6 , wherein the second additional heavy chain CDRs comprises the amino acid sequence of SEQ ID NO: 26. 8 . The antibody or antibody fragment of any of claims 3 - 7 , further comprising at least one light chain CDR. 9 . The antibody or antibody fragment of claim 8 , wherein the at least one light chain CDR comprises the amino acid sequence of SEQ ID NO: 27. 10 . The antibody or antibody fragment of claim 9 , further comprising a second light chain CDR. 11 . The antibody or antibody fragment of claim 10 , wherein the second light chain CDR comprises the amino acid sequence of SEQ ID NO: 28. 12 . The antibody or antibody fragment of claim 11 , further comprising a third light chain CDR. 13 . The antibody or antibody fragment of claim 12 , wherein the third light chain CDR comprises the amino acid sequence of SEQ ID NO: 29. 14 . A method of treating a Hendra virus or Nipah virus infection comprising administering the antibody or antibody fragment of claim 3 to a subject which has been infected with Hendra or Nipah virus. 15 . A method of reducing the likelihood of a subject developing a disease caused by Hendra virus or Nipah virus, the method comprising administering the antibody or antibody fragment claim 3 to a subject prior to Hendra virus infection or Nipah virus infection. 16 . A nucleic acid encoding the peptide of claim 1 . 17 . A vector comprising the nucleic acid of claim 16 . 18 . A host cell comprising the vector of claim 17 . 19 . A method of making a peptide comprising an amino acid of SEQ ID NO: 2, SEQ ID NO: 3; SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22 and SEQ ID NO: 23, the method comprising culturing the host cell of claim 18 under conditions suitable for protein expression and isolating the peptide. 20 . An antibody that binds to the four hydrophobic pockets of the G glycoprotein head of Hendra virus or Nipah virus.

Assignees

Inventors

Classifications

  • Complementarity determining region [CDR] · CPC title

  • Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value · CPC title

  • Antagonist effect on antigen, e.g. neutralization or inhibition of binding · CPC title

  • for RNA viruses · CPC title

  • C07K16/11Primary

    Paramyxoviridae (F); Pneumoviridae (F), e.g. respiratory syncytial virus [RSV] · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US2016272697A2 cover?
The invention described herein provides novel peptides. The novel peptides are useful alone or as portions of larger molecules, such as antibodies or antibody fragments, that can be used to treat or prevent infection of Nipah virus and/or Hendra virus.
Who is the assignee on this patent?
Henry M Jackson Found Advancement Military Medicine Inc
What technology area does this patent fall under?
Primary CPC classification C07K16/11. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Sep 22 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A2). 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).