Hpv vaccine manufacture

US2024131140A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2024131140-A1
Application numberUS-202218276578-A
CountryUS
Kind codeA1
Filing dateFeb 9, 2022
Priority dateFeb 11, 2021
Publication dateApr 25, 2024
Grant date

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Described are methods for the preparation of a HPV vaccine composition by, for example (i) adsorbing one or more HPV antigen(s) on a metallic salt and, then (ii) adding a non adsorbed glycolipid based TLR4 ligand to the mixture obtained in (i). Resulting HPV vaccine compositions and uses thereof are also described.

First claim

Opening claim text (preview).

1 . A method for the preparation of a human papillomavirus (HPV) vaccine composition comprising the following steps: (i) adsorption of one or more HPV antigen(s) on a metallic salt, and (ii) addition of a non adsorbed glycolipid based TLR4 ligand to the mixture obtained in 2 . The method according to claim 1 , wherein the one or more HPV antigen(s) are selected from the group consisting of HPV late proteins L1, L2, chimeric L1 and chimeric L1/L2 proteins. 3 . The method according to claim 2 , wherein the one or more HPV antigen(s) are selected from HPV L1 VLPs (virus like particles). 4 . The method according to claim 3 , wherein the HPV L1 VLPs are produced in E. coli, yeast cells or in a baculovirus expression system. 5 . The method according to claim 4 , wherein the HPV L1 VLPs are produced in E. coli. 6 . The method according to claim 1 , wherein each of the one or more HPV antigen(s) are from a HPV type selected from HPV types 6, 11, 16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 67, 68, 70, 73 and 82, more preferably from HPV types 6, 11, 16, 18, 31, 33, 115, 52 and 58. 7 . The method according to claim 1 , wherein the one or more HPV antigen(s) comprise HPV antigen(s) from HPV types 16 and 18. 8 . The method according to claim 1 , wherein the one or more HPV antigen(s) comprise HPV antigen(s) from HPV types 6, 11, 16, and 18. 9 . The method according to claim 1 , wherein the one or more HPV antigen(s) comprise HPV antigen(s) from HPV types 6, 11, 16, 18, 31, 33, 45, 52 and 58. 10 . The method according to claim 9 , wherein the one or more HPV antigen(s) further comprise HPV antigen(s) from HPV types 35, 39 and/or 59. 11 . The method according to claim 1 , wherein the one or more HPV antigen(s) comprise L1 VLPs from HPV types 16 and 18. 12 . The method according to claim 1 , wherein the one or more HPV antigen(s) comprise L1 VLPs from HPV types 6, 11, 16, and 18. 13 . The method according to claim 1 , wherein the one or more HPV antigen(s) comprise or consist of L1 VLPs from HPV types 6, 11, 16, 18, 31, 33, 45, 52 and 58. 14 . The method according to claim 13 , wherein the one or more HPV antigen(s) further comprise L1 VLPs from HPV types 35, 39 and/or 59 L1 VLPs. 15 . The method according to claim 1 , wherein the metallic salt comprises aluminum. 16 . The method according to claim 15 , wherein the metallic salt is selected from the group consisting of AlOOH, AlPO 4 , AlHO 9 PS −3 and AlHO 5 P. 17 . The method according to claim 1 , wherein the glycolipid based TLR4 agonist is selected from MPL, GLA, SLA, OM-174, CCL-34, RC-529, PET-Lipid A, ONO-4007 and dLOS. 18 . The method according to claim 1 further comprising the step of adding a metallic salt to the HPV vaccine composition. 19 . The method of claim 1 , wherein the one or more HPV antigen(s) comprise L1 VLPs from HPV types 6, 11, 16, 18, 31, 33, 45, 52, and 58, the metallic salt comprises aluminum, and the glycolipid based TLR4 agonist is MPL. 20 . A HPV vaccine composition obtained by the method of claim 1 . 21 . The HPV vaccine composition of claim 20 wherein the metallic ion which is part of the metallic salt is Al + and the amount of Al + in the HPV vaccine composition is from 100 to 500 μg/dose. 22 . The HPV vaccine composition of claim 20 wherein the glycolipid based TLR4 ligand is MPL and the amount of MPL in the HPV vaccine composition is from 10 to 50 μg/dose. 23 . The HPV vaccine composition of claim 20 , wherein the ratio of glycolipid based TLR4 ligand:metallic salt in the HPV vaccine composition is from 1:2 to 1:20. 24 . (canceled) 25 . The HPV vaccine of claim 20 for preventing or treating a HPV infection or associated disease in a subject. 26 . A method of preventing or treating an infection or disease caused by HPV comprising the administration of an effective amount of the HPV vaccine of to claim 20 to a patient in need thereof. 27 . The method according to claim 1 , wherein the one or more HPV antigen(s) consist of L1 VLPs from HPV types 6, 11, 16, 18, 31, 33, 45, 52 and 58.

Assignees

Inventors

Classifications

  • A61K39/12Primary

    Viral antigens · CPC title

  • Inorganic adjuvants · CPC title

  • Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein · CPC title

  • Multivalent vaccine · CPC title

  • for DNA viruses · CPC title

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What does patent US2024131140A1 cover?
Described are methods for the preparation of a HPV vaccine composition by, for example (i) adsorbing one or more HPV antigen(s) on a metallic salt and, then (ii) adding a non adsorbed glycolipid based TLR4 ligand to the mixture obtained in (i). Resulting HPV vaccine compositions and uses thereof are also described.
Who is the assignee on this patent?
Glaxosmithkline Biologicals Sa, Xiamen Innovax Biotech Co Ltd
What technology area does this patent fall under?
Primary CPC classification A61K39/12. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Apr 25 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).