IP Library › Granted Patent US 9,023,364
Granted Patent B2
US 9,023,364 · App. 12/452,305 · Granted May 5, 2015

Vaccine antigen capable of inducing cross-reacting and neutralizing antibody against high-risk-type human papillomavirus

Inventors: Tadahito Kanda (Tokyo, JP); Kazunari Kondo (Tokyo, JP)
Assignee: Japan Health Sciences Foundation
A61K39/12C07K14/005C12N7/00A61K2039/5258C07K2319/40C12N2710/20022C12N2710/20034
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Quick Facts
Patent No.
US 9,023,364
App. No.
12/452,305
Granted
May 5, 2015
Kind
B2
Abstract

Disclosed is a vaccine antigen capable of inducing a cross-reacting and neutralizing antibody directed against a high-risk-type human papillomavirus. Specifically disclosed are: a chimeric protein comprising an L2-epitope of a human papillomavirus (HPV) type-16 inserted in a loop region of a human papillomavirus type-16 L1 protein; and a capsid which is a particle formed by the chimeric protein. The loop region to which the L2-epitope is to be inserted is located between an amino acid residue at position-430 and an amino acid residue at position-433. The L2-epitope has an amino acid sequence represented by any one of the following formulae: LYKTCKQAGTCPPDIIPKVEG (SEQ ID NO: 2) (18-38 L2-epitope); GGLGIGTGSGTGGRTGYIPL (SEQ ID NO: 3) (56-75 L2-epitope); and DPVGPLDPSIVSLVEESSFI (SEQ ID NO: 4) (96-115 L2-epitope).

Claims (14)

1. A capsid which is an aggregate formed by assembly of chimeric protein composed of human papillomavirus (HPV) 16 L1 protein and an HPV16 L2 epitope inserted in the loop region of the HPV16 L1 protein, wherein

the region for insertion of the L2 epitope is a region of amino acids 430 to 433 and

the L2 epitope has an amino acid sequence represented by:

GGLGIGTGSGTGGRTGYIPL (SEQ ID NO: 3) (hereinafter, referred to as 56-75 L2 epitope).

2. The capsid according to claim 1 , wherein the aggregate is an aggregate formed by assembly of multiple pentamer capsomeres, wherein each pentamer capsomere is composed of five chimeric protein molecules.

3. The capsid according to claim 2 , wherein the aggregate formed by assembly of multiple pentamer capsomeres has a particle structure.

4. The capsid according to claim 3 , wherein the number of the pentamer capsomeres constituting the aggregate is in the range of 65 to 80.

5. The capsid according to claim 3 , wherein the number of the pentamer capsomeres constituting the aggregate is 72.

6. The capsid according to any one of claims 1 and 2 to 5 , which is used for production of an L1 capsid immunogenic composition.

7. A chimeric protein composed of human papillomavirus (HPV) 16 L1 protein and an HPV16 L2 epitope inserted in the loop region of the HPV16 L1 protein, wherein

the loop region for insertion of the L2 epitope is a region of amino acids 430 to 433, and

the L2 epitope has an amino acid sequence represented by:

GGLGIGTGSGTGGRTGYIPL (SEQ ID NO: 3) (hereinafter, referred to as 56-75 L2 epitope).

8. A method of producing the capsid according to any one of claims 1 and 2 to 5 , wherein the capsid is formed by assembly of the chimeric protein according to claim 7 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2020
From: JAPAN HEALTH SCIENCES FOUNDATION
To: JAPAN AS REPRESENTED BY DIRECTOR-GENERAL OF NATIONAL INSTITUTE OF INFECTIOUS DISEASES
Reel/Frame 054718/0520 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 25, 2010
From: KANDA, TADAHITO; KONDO, KAZUNARI
To: JAPAN HEALTH SCIENCES FOUNDATION
Reel/Frame 024134/0514 →
Priority Claims (1)
JP 2007-167154 · Jun 26, 2007 · national
Continuity (1)
Related Publication 20100183648A1 · Jul 22, 2010