Vaccine composition

US10076491B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10076491-B2
Application numberUS-201414166965-A
CountryUS
Kind codeB2
Filing dateJan 29, 2014
Priority dateFeb 5, 2013
Publication dateSep 18, 2018
Grant dateSep 18, 2018

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 provides a vaccine composition containing an antigen for inducing cellular immunity, comprising at least one first cellular immunity induction promoter.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for inducing cellular immunity in a subject, comprising transdermally administering, to intact skin or under mildly irritating conditions, an immunogenic composition comprising: an antigen, at least one first cellular immunity induction promoter selected from the group consisting of a cyclooxygenase inhibitor, a prostaglandin receptor antagonist, a prostaglandin receptor agonist, a TSLP production inhibitor, an adenylate cyclase inhibitor, an omega-3 fatty acid, a PPAR agonist, a dopamine receptor antagonist, a dopamine receptor agonist, a histamine receptor agonist, a histamine receptor antagonist, a serotonin receptor agonist, a serotonin receptor antagonist, a vasopressin receptor antagonist, a vasopressin receptor agonist, a muscarine receptor antagonist, a muscarine receptor agonist, an adrenergic receptor antagonist, an adrenergic receptor agonist, an angiotensin receptor agonist, a GABA receptor agonist, a thrombin receptor antagonist, a thrombin receptor agonist, an opioid receptor agonist, an ADP receptor agonist, a leukotriene receptor antagonist, a leukotriene receptor agonist, a melatonin receptor agonist, a somatostatin receptor agonist, a cannabinoid receptor agonist, a sphingosine-1 phosphate receptor agonist, a metabotropic glutamate receptor agonist, a phospholipase A2 inhibitor, a TGF-β production inhibitor, and a Th2 cytokine inhibitor, and a TLR ligand other than a TLR9 ligand. 2. The method according to claim 1 , wherein the composition is administered to the skin under a mildly irritating condition. 3. The method according to claim 2 , wherein the mildly irritating condition is a condition under which transepidermal water loss (TEWL) in a model animal for skin irritation evaluation before the administration of the composition is 50 g/hm 2 or less. 4. The method according to claim 2 , wherein the mildly irritating condition is a condition under which the cutaneous TSLP level in a model animal for skin irritation evaluation at completion of the administration of the composition is 10000 pg/mg protein or less. 5. The method according to claim 1 , wherein the method is for the treatment of a cancer. 6. The method according to claim 1 , wherein the method is for the treatment of a viral disease. 7. The method according to claim 1 , wherein the TLR ligand is a TLR4 ligand. 8. The method according to claim 7 , wherein the TLR4 ligand is a lipopolysaccharide (LPS) derived from bacteria or plants. 9. The method according to claim 8 , wherein the TLR4 ligand is a lipopolysaccharide (LPS) derived from Pantoea genus. 10. The method according to claim 1 , wherein the TLR ligand is a TLR7 and/or TLR8 ligand. 11. The method according to claim 10 , wherein the TLR7 and/or TLR8 ligand is imiquimod. 12. The method according to claim 1 , wherein the first cellular immunity induction promoter is a cyclooxygenase inhibitor. 13. The method according to claim 12 , wherein the cyclooxygenase inhibitor is selected from etodolac, loxoprofen, indomethacin, aspirin, diclofenac, ketoprofen, celecoxib, valdecoxib, and derivatives thereof, and pharmacologically acceptable salts thereof. 14. The method according to claim 12 , wherein the cyclooxygenase inhibitor is loxoprofen. 15. The method according to claim 11 , wherein the cyclooxygenase inhibitor is loxoprofen.

Assignees

Inventors

Classifications

  • Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics · CPC title

  • Antineoplastic agents · CPC title

  • Drugs for immunological or allergic disorders · CPC title

  • Immunostimulants · CPC title

  • characterised by the route of administration · 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 US10076491B2 cover?
The invention provides a vaccine composition containing an antigen for inducing cellular immunity, comprising at least one first cellular immunity induction promoter.
Who is the assignee on this patent?
Nitto Denko Corp
What technology area does this patent fall under?
Primary CPC classification A61K31/407. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Sep 18 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). 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).