IP Library Granted Patent US 8,784,830
Granted Patent B2
US 8,784,830 · App. 13/380,425 · Granted Jul 22, 2014

Antigen peptide and use thereof

Inventors: Kenichiro Hasumi (Tokyo, JP); Mikio Kuraya (Tokyo, JP)
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Quick Facts
Patent No.
US 8,784,830
App. No.
13/380,425
Granted
Jul 22, 2014
Kind
B2
Abstract

In order to provide an effective vaccine against infection with Propionibacterium acnes , the present invention provides a peptide which is a peptide consisting of a specific amino acid sequence or a peptide consisting of an amino acid sequence derived from the specific amino acid sequence by deletion, substitution, insertion, or addition of one or more amino acids, the peptide suppressing, by immune response, inflammation caused by infection with Propionibacterium acnes.

Claims (13)

1. A peptide consisting of the amino acid sequence of SEQ NO. 1.

2. A fusion peptide, which is in a form of a multivalent antigen peptide comprising two or more of the peptide of claim 1 operably linked.

3. A pharmaceutical composition for reducing inflammation caused by Propionibacterium acnes , comprising the fusion peptide as set forth in claim 2 and a pharmaceutically acceptable carrier.

4. The pharmaceutical composition of claim 3 , which is in the form of a solution, a suspension, a tablet, a pill, a capsule, a sustained release formulation or a powder.

5. The pharmaceutical composition of claim 3 , further comprising an adjuvant.

6. The pharmaceutical composition of claim 5 , wherein the adjuvant is selected from the group consisting of aluminum hydroxide, aluminum phosphate, aluminum potassium sulfate (alum), beryllium sulfate, silica, kaoline, carbon, water-in-oil type emulsion, oil-in-water type emulsion, Muramyl dipeptide, bacterial endotoxin, fat X, Bordetella pertussis, Corynebacterium parvum , polyribonucleotide, sodium alginate, lanoline, lysolecithin, vitamin A, sponin, liposome, levamisole, DEAE-dextran, block copolymer, and combinations thereof.

7. The fusion peptide of claim 2 , wherein the two of more of the peptides are operably linked by a linker.

8. A composition, comprising:

the peptide as set forth in claim 1 , or a fusion peptide which is in a form of a multivalent antigen peptide comprising two or more of the peptide of claim 1 operably linked.

9. A pharmaceutical composition for reducing inflammation caused by Propionibacterium acnes , comprising the peptide as set forth in claim 1 and a pharmaceutically acceptable carrier.

10. The pharmaceutical composition of claim 9 , which is in the form of a solution, a suspension, a tablet, a pill, a capsule, a sustained release formulation or a powder.

11. The pharmaceutical composition of claim 9 , further comprising an adjuvant.

12. The pharmaceutical composition of claim 11 , wherein the adjuvant is selected from the group consisting of aluminum hydroxide, aluminum phosphate, aluminum potassium sulfate (alum), beryllium sulfate, silica, kaoline, carbon, water-in-oil type emulsion, oil-in-water type emulsion, Muramyl dipeptide, bacterial endotoxin, fat X, Bordetella pertussis, Corynebacterium parvum , polyribonucleotide, sodium alginate, lanoline, lysolecithin, vitamin A, sponin, liposome, levamisole, DEAE-dextran, block copolymer, and combinations thereof.

Continuity (2)
Provisional Application 61396574 · May 27, 2010
Related Publication 20120301495A1 · Nov 29, 2012