Anti-dengue vaccines and antibodies

Patent metadata

Field	Value
Publication number	US-12415836-B2
Application number	US-202117510930-A
Country	US
Kind code	B2
Filing date	Oct 26, 2021
Priority date	Jul 23, 2014
Publication date	Sep 16, 2025
Grant date	Sep 16, 2025

Abstract

A Dengue virus Envelope Dimer Epitope (EDE) wherein the EDE: c) spans the polypeptides of a Dengue virus Envelope polypeptide dimer; and/or d) is presented on a dimer of Envelope proteins; and/or c) is formed from consecutive or nonconsecutive residues of the envelope polypeptide dimer, 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 and DENV-4. The EDE may be a stabilized recombinant dengue virus 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 covalently stabilized with at least one sulfhydryl-reactive crosslinker between the two sE monomers, and/or covalently stabilized by linking the two sE monomers through modified sugars; 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 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. A compound, for example an antibody or antibody fragment that can neutralise more than one Dengue virus serotype, for example an antibody that can bind to an EDE of the invention.

First claim

The invention claimed is:

1. A composition comprising an adjuvant and a compound that binds to an E-Dimer Epitope (EDE), wherein the compound is an antibody comprising a heavy chain comprising CDR regions and light chain comprising CDR regions, or antigen binding portion thereof,
wherein the antibody, or antigen binding portion thereof, comprises:
a) a heavy chain variable region comprising the amino acid sequences SEQ ID NO: 5, 6 and 7 and a light chain variable region comprising the amino acid sequences SEQ ID NO: 17, 18 and 19; or
b) a heavy chain variable region comprising the amino acid sequences SEQ ID NO: 8, 9 and 10 and a light chain variable region comprising the amino acid sequences SEQ ID NO: 20, 21 and 22; or
c) a heavy chain variable region comprising the amino acid sequences SEQ ID NO: 11, 12 and 13 and a light chain variable region comprising the amino acid sequences SEQ ID NO: 23, 24 and 25; or
d) a heavy chain variable region comprising the amino acid sequences SEQ ID NO: 14, 15, and 16 and a light chain variable region comprising the amino acid sequences SEQ ID NO: 26, 27 and 28;

wherein the EDE comprises a stabilized recombinant dengue virus envelope glycoprotein E ectodomain (sE) dimer, a dimer of Envelope proteins, or the antigenic portion thereof, or consecutive or non-consecutive residues of the envelope polypeptide dimer, held within a heterologous scaffold protein, and
wherein said antibody or fragment thereof binds the five polypeptide segments of the dengue virus glycoprotein E ectodomain consisting of the residues 67-74, residues 97-106, residues 307-314, residues 148-159 and residues 243-251, wherein the amino acid residue position of each sE monomer is numbered according to SEQ ID NO: 132, SEQ ID NO: 133, SEQ ID NO: 134, and SEQ ID NO: 135.

2. The composition according to claim 1 , wherein the stabilised EDE is any one or more of:
a) a dimer wherein the monomer is selected from the group consisting of: the DENV-1 sE of SEQ ID NO: 132, the DENV-2 SE of SEQ ID NO: 133 the DENV-3 SE of SEQ ID NO: 134, the DENV-4 sE of SEQ ID NO: 135 and a mutant sE thereof having at least one mutation selected among H27F, H27W, L107C, F108C, H244F, H244W, S255C, A259C, T/S262C, T/A265C, L278F, L292F, L294N, A313C and T315C and optionally at least one additional mutation selected from the group consisting of Q227N, E174N and D329N;
b) a homodimer of two identical recombinant sE or a heterodimer of two different recombinant sE;
c) a dimer which is glycosylated at position 67, at position 153 of each sE monomer, or both;
d) a dimer which is covalently stabilized with at least one, two or three disulphide inter-chain bonds between the two sE monomers;
e) a homodimer of mutant sE having each the mutation A259C or S255C and wherein the residues 259C or 255C are linked together through a disulphide inter-chain bond;
f) a dimer which is a heterodimer of a mutant sE having the mutation A259C and a mutant sE having the mutation S255C, wherein the residues 259C and 255C are linked together through a disulphide inter-chain bond;
g a homodimer of mutant sE having each the mutations F108C and T315C or a homodimer of mutants sE having each the mutations L107C and A313C wherein the residues 108C and 315C or the residues 107C and 313C are linked together through a disulphide inter-chain bond;
h) a heterodimer of a mutant sE having the mutations F108C and A313C and a mutant sE having the mutations L107C and T315C wherein the residues 108C and 313C are linked respectively to the residues 315C and 107C through a disulphide inter-chain bond between the two sE monomers;
i) a dimer, selected from the group consisting of a homodimer of mutants sE having each the mutations A259C, F108C and T315C, a homodimer of mutants sE having each the mutations S255C, F108C and T315C, a homodimer of mutants sE having each the mutations A259C, L107C and A313C, and a homodimer of mutants sE having each the mutations A255C, L107C and A313C as defined above, wherein the residues 259C, 255C, 108C, 315C, 107C and 313C are linked respectively to the residues 259C, 255C, 315C, 108C, 313C and 107C through disulphide inter-chain bonds;
j) a heterodimer of a mutant sE having the mutations A259C, F108C and T315C and a mutant sE having the mutations S255C, F108C and T315C as defined above, wherein the residues 259C, 108C and 315C are linked respectively to the residues 255C, 315C and 108C through disulphide inter-chain bonds;
k) a heterodimer of a mutant sE having the mutations S255C, L107C and A313C and a mutant sE having the mutations A259C, L107C and A313C, wherein the residues 255C, 107C and 313C are linked respectively to the residues 259C, 313C and 107C through disulphide inter-chain bonds;
l) a dimer which is covalently stabilized with at least one, two or three, sulfhydryl-reactive crosslinkers (also called thiol-reactive crosslinkers) between the sE monomers;
m) is a homodimer of mutant sE having each the mutation T/S262C or T/A265C, wherein the residues 262C or 265C are linked together through a sulfhydryl-reactive crosslinker;
n) a heterodimer of a mutant sE having the mutation T/S262C as defined above and a mutant sE having the mutation T/A265C, wherein the residues 262C and 265C are linked together through a sulfhydryl-reactive crosslinker;
o) a homodimer or a heterodimer of a mutant sE wherein at least one of the amino acid residues 1-9, 25-30, 238-282, 96-111 311-318 of sE is mutated to cysteine and a mutant sE wherein at least one of the amino acid residues 1-9, 25-30, 238-282, 96-111 311-318 of sE is mutated to cysteine, and wherein the mutated cysteine residues are linked together through a sulfhydryl-reactive crosslinker;
p) a dimer which is covalently stabilized by linking the two monomers through modified sugars;
q) a homodimer or heterodimer of mutant sE, wherein:
one sE monomer has at least one mutation which introduces a glycosylation site, and wherein the mutated amino acid residue is glycosylated with a modified sugar bearing an X functional group, and the other sE monomer has at least one mutation which introduces a glycosylation site, and wherein the mutated amino acid residue is glycosylated with a modified sugar bearing a Y functional group, and wherein both mutated residues are joined together through the modified sugars by reacting, specifically by click chemistry, the X functional group of the sugar of the first sE monomer with the Y functional group of the sugar of the other sE monomer;

r) a dimer which is non-covalently stabilized by filling the cavities of said dimer at the dimer interface by substituting at least one amino acid in the amino acid sequence of one or the two monomers, with bulky side chain amino acids;
s) a dimer which is 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 within regions forming cavities at the dimer interface or in domain 1 (D1)/domain 3 (D3) linker of each monomer increasing hydrophobic interactions between the two sE monomers;
t) a homodimer or heterodimer of two recombinant sE as defined above, wherein one of the recombinant sE or the two recombinant sE have at least one mutation selected from the group consisting of H27F, H27W, H244F, H244W, and L278F;
u) a dimer which is non-covalently stabilized in domain 1 (D1)/domain 3 (D3) linker of each monomer, by substituting amino acids in the amino acid sequence of one or the two monomers with at least one bulky side chain amino acid;
v) a dimer which is a homodimer or heterodimer of two recombinant sE as defined above, wherein one of the recombinant sE or the two recombinant sE have at least one mutation selected from the group consisting of L292F and L294N,
wherein the amino acid residue position of each sE monomer is numbered according to SEQ ID NO: 132,

Assignees

• Univ Oxford Innovation Ltd
• Univ Paris Saclay

Inventors

• Screaton Gavin
• Mongkolsapaya Juthathip
• Rouvinski Alexander
• Guardado-Calvo Pablo
• Barba-Spaeth Giovanna
• Duquerroy Stéphane
• Vaney Marie-Christine
• Rey Felix Augusto

Classifications

• C07K16/116

  Togaviridae (F); Matonaviridae (F); Flaviviridae (F) · CPC title

• C07K2317/76

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

• C07K2317/56

  variable (Fv) region, i.e. VH and/or VL · CPC title

• A61K47/6841

  the antibody targeting a RNA virus · CPC title

• Y02A50/30

  Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change · CPC title