Lentiviral vector-based Japanese encephalitis immunogenic composition

Patent metadata

Field	Value
Publication number	US-11779640-B2
Application number	US-202016794854-A
Country	US
Kind code	B2
Filing date	Feb 19, 2020
Priority date	Dec 11, 2014
Publication date	Oct 10, 2023
Grant date	Oct 10, 2023

Abstract

The present invention relates to a lentiviral vector-based Japanese encephalitis (JE) immunogenic composition. The present invention is directed to a recombinant lentiviral vector expressing the precursor of membrane (prM) and the envelope (E) protein, in particular glycoprotein of a Japanese encephalitis virus (JEV) or immunogenic fragments thereof. The present invention also provides cells expressing the lentiviral vector, uses and methods to prevent a JEV infection in a mammalian host, especially in a human or an animal host, in particular a pig or a piglet, preferably a domestic pig or a domestic piglet.

First claim

The invention claimed is:

1. A method of prophylactically treating against JEV infection in a mammal, comprising administering recombinant lentiviral vector particles expressing a recombinant lentiviral vector genome to the mammal, wherein the recombinant lentiviral vector particles are able to elicit a protective immune response against genotypes 1, 3, and 5 of JEV that is conferred within about one week after a prime/boost administration of the composition;
(i) wherein said recombinant lentiviral vector genome comprises lentiviral cis-active elements including long terminal repeats (LTRs) or modified LTRs including partially deleted 3′LTR, psi (w) packaging signal, Rev responsive element (RRE) and DNA flap central polypurine tract (cPPT)/central termination sequence (CTS), together with a transcription unit encoding the precursor of membrane (prM) of SEQ ID NO: 6, and the envelope (E) protein of a Japanese encephalitis virus (JEV), wherein the E protein is either the full-length E protein of SEQ ID NO: 9, or its soluble form of SEQ ID NO: 12;
(ii) wherein said particles are pseudotyped with a vesicular stomatitis virus glycoprotein G (VSV-G) protein; and
(iii) wherein said transcription unit encodes the amino acid sequence of SEQ ID NO: 3.

2. The method according to claim 1 , wherein in the lentiviral 3′-LTR the promoter and the activator of the U3 region have been deleted, and wherein the polynucleotide encoding the prM and E proteins is placed under the control of a heterologous promoter.

3. The method according to claim 2 , wherein the heterologous promoter is the cytomegalovirus immediate early (CMVie) promoter.

4. The method according to claim 1 , wherein the polynucleotide encoding the prM protein has the sequence of SEQ ID NO: 5, the polynucleotide encoding the full-length E protein has the sequence of SEQ ID NO: 8 and the polynucleotide encoding the soluble form of the E protein has the sequence of SEQ ID NO: 11.

5. The method according to claim 1 , wherein the lentiviral vector genome is derived from the genome of HIV.

6. The method according to claim 5 , wherein the genome of HIV is of HIV-1.

7. The method according to claim 1 , wherein the lentiviral vector genome is derived from the genome of FIV.

8. The method according to claim 1 , wherein the lentiviral vector genome is replication-incompetent as a result of deletion of all or part of the gag and pol genes of the lentiviral genome or mutation in the gag and pol genes of the lentiviral genome, so that the gag and pol genes are not capable of encoding functional GAG and POL proteins.

9. The method according to claim 1 , wherein the mammal is a pig or a piglet.

10. The method according to claim 1 , wherein the lentiviral vector particles are integration defective as a result of mutation or deletion in the pol gene of the lentivirus.

11. The method according to claim 1 , wherein the lentiviral vector particles are administered at a dose sufficient to elicit a protective antibody response against JEV prM and/or E protein(s).

12. The method according to claim 1 , wherein the method comprises administering said recombinant lentiviral vector particles in a prime-boost regimen.

13. The method according to claim 12 , wherein the lentiviral vector particles for priming the immunological response and the lentiviral vector particles for boosting the response are pseudotyped with different non-cross reacting VSV-G envelope proteins.

14. The method according to claim 1 , wherein the JEV is a JEV of a genotype selected from G1, G3 and G5.

15. The method according to claim 1 , wherein the JEV is a JEV of genotype G3.

16. The method according to claim 15 , wherein the JEV is a JEV of the strain RP-9 or a JEV of the strain Nakayama.

17. The method according to claim 1 , wherein said particles are in admixture with a pharmaceutically acceptable vehicle, and/or an adjuvant.

Assignees

• Pasteur Institut
• Centre Nat Rech Scient

Inventors

• Charneau Pierre
• Despres Philippe
• De Wispelaere Melissanne
• Souque Philippe
• Frenkiel Marie-Pascale

Classifications

• A61K39/12 Primary

  Viral antigens · CPC title

• A61K9/19

  lyophilised {, i.e. freeze-dried, solutions or dispersions (lyophilised products with subsequent particle size reduction A61K9/14; granules or pellets made by lyphilisation A61K9/1682; solid oral dosage forms made by lyophilisation A61K9/2095; lyophilisation additives A61K47/00)} · CPC title

• A61K47/26

  Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin · CPC title

• C07K14/005

  from viruses · CPC title

• C07K14/1825 Primary

  Flaviviruses or Group B arboviruses, e.g. yellow fever virus, japanese encephalitis, tick-borne encephalitis, dengue · CPC title