Invention Grant
- Patent Title: Neutralising antibody against dengue for use in a method of prevention and/or treatment of zika infection
-
Application No.: US16308745Application Date: 2017-06-09
-
Publication No.: US11111274B2Publication Date: 2021-09-07
- Inventor: Félix Rey , Giovanna Barba Spaeth , Marie-Christine Vaney , Alexander Rouvinski , Gavin Screaton , Juthathip Mongkolsapaya
- Applicant: IMPERIAL INNOVATIONS LTD , INSTITUT PASTEUR
- Applicant Address: GB London; FR Paris
- Assignee: IMPERIAL INNOVATIONS LTD,INSTITUT PASTEUR
- Current Assignee: IMPERIAL INNOVATIONS LTD,INSTITUT PASTEUR
- Current Assignee Address: GB London; FR Paris
- Agency: Pabst Patent Group LLP
- Priority: GB1610162 20160610
- International Application: PCT/GB2017/051692 WO 20170609
- International Announcement: WO2017/212291 WO 20171214
- Main IPC: A61K39/00
- IPC: A61K39/00 ; A61K35/17 ; A61K38/00 ; A61K39/12 ; C07K14/705 ; C07K14/005 ; A61P31/14 ; C07K16/10 ; G01N33/569 ; C07K14/18

Abstract:
A flavivirus Envelope Dimer Epitope (EDE) for use in vaccinating an individual against one or more flaviviruses wherein the EDE is a stabilized recombinant flavivirus, optionally dengue virus and/or zika envelope glycoprotein E ectodomain (sE) dimer, wherein the dimer is: covalently stabilized with at least one disulphide inter-chain bond between the two sE monomers, and/or non-covalently stabilized by substituting at least one amino acid residue in the amino acid sequence of at least one sE monomer with at least one bulky side chain amino acid, at the dimer interface or in domain 1 (D1)/domain 3 (D3) linker of each monomer, covalently stabilized with at least one sulfhydryl-reactive crosslinker between the two sE monomers, and/or covalently stabilised by being formed as a single polypeptide chain, optionally with a linker region, optionally a Glycine Serine rich linker region, separating the sE sequences, and/or covalently stabilized by linking the two sE monomers through modified sugars; and/or, wherein the dimer is a homodimer or heterodimer of native and/or mutant envelope polypeptides, from any one or two of DENV-1, DENV-2, DENV-3, DENV-4, Zika or other flavivirus; and wherein the one or more flaviviruses is selected from zika virus; zika virus and dengue virus; zika virus and other flaviviruses; flaviviruses other than dengue. The EDE may be a homodimer or heterodimer of native and/or mutant envelope polypeptides, from any one or two of DENV-1, DENV-2, DENV-3, DENV-4 and Zika. An isolated neutralizing antibody or antigen binding fragment thereof directed against the EDE as defined in any one of claims 1 to 29, optionally wherein said antibody or fragment thereof binds the five polypeptide segments of the dengue virus glycoprotein E ectodomain (sE) consisting of the residues 67-74, residues 97-106, residues 307-314, residues 148-159 and residues 243-251, or corresponding residues of the flavivirus or Zika virus glycoprotein E ectodomain, or consisting of Zika PF13 residues 67-77, residues 97-106, residues 313-315, residues 243-253, residue K373 or corresponding residues of the flavivirus glycoprotein E ectodomain, optionally wherein binding is unaffected by presence or absence of dengue N153 (Zika N154) glycan or corresponding residue, for use in a method for prevention and/or treatment of infection by one or more flaviviruses, wherein the one or more flaviviruses is selected from zika virus; zika virus and dengue virus; zika virus and other flaviviruses; flaviviruses other than dengue.
Public/Granted literature
Information query