IP Library Granted Patent US 9,273,102
Granted Patent B2
US 9,273,102 · App. 14/351,423 · Granted Mar 1, 2016

Peptides derived from

Inventors: Niels Iversen Møller (Gilleleje, DK); Andreas Mattsson (København, DK)
C07K14/205A61K39/02A61K39/00
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Quick Facts
Patent No.
US 9,273,102
App. No.
14/351,423
Granted
Mar 1, 2016
Kind
B2
Abstract

Disclosed are polypeptides for Campylobacter jejuni that are useful as immunogenic agents for vaccine use. Also disclosed are nucleic acid fragments encoding the polypeptides as well as compositions, methods and molecular biology tools derived from or related to the proteins.

Claims (29)

1. A polypeptide which is fused or conjugated to an immunogenic carrier molecule, wherein said polypeptide comprises:

a) an amino acid sequence selected from the group consisting of any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30, or

b) an amino acid sequence consisting of at least 35 contiguous amino acid residues from any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30, or

c) an amino acid sequence having a sequence identity of at least 60% with the amino acid sequence of any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30, or

d) an amino acid sequence having a sequence identity of at least 60% with the amino acid sequence of at least 35 contiguous amino acid residues from any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30,

said polypeptide being antigenic in a mammal.

2. The polypeptide according to claim 1 , wherein the at least 35 contiguous amino acid residues have, as their N-terminal amino acid residue, amino acid residue 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, and 47 in any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28 and 30.

3. The polypeptide according to claim 1 , wherein the at least 35 contiguous amino acid residues have, as their N-terminal amino acid residue, amino acid residue 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, and 243 in any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28 and 30.

4. The polypeptide according to claim 1 , wherein the immunogenic carrier molecule is a polypeptide that induces T-helper lymphocyte responses in a majority of humans.

5. A pharmaceutical composition comprising a polypeptide and a pharmaceutically acceptable carrier, vehicle or diluent, and which further comprises an immunological adjuvant, wherein said polypeptide comprises:

a) an amino acid sequence selected from the group consisting of any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30, or

b) an amino acid sequence consisting of at least 35 contiguous amino acid residues from any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30, or

c) an amino acid sequence having a sequence identity of at least 60% with the amino acid sequence of any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30, or

d) an amino acid sequence having a sequence identity of at least 60% with the amino acid sequence of at least 35 contiguous amino acid residues from any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30,

said polypeptide being antigenic in a mammal,

or wherein said polypeptide is according to claim 1 .

6. The pharmaceutical composition according to claim 5 , wherein the adjuvant is an aluminum based adjuvant.

7. A method for inducing immunity in an animal by administering at least once an immunogenically effective amount of a polypeptide or a pharmaceutical composition according to claim 5 or 6 so as to induce adaptive immunity against C. jejuni in the animal, wherein said polypeptide comprises:

a) an amino acid sequence selected from the group consisting of any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30, or

b) an amino acid sequence consisting of at least 35 contiguous amino acid residues from any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30, or

c) an amino acid sequence having a sequence identity of at least 60% with the amino acid sequence of any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30, or

d) an amino acid sequence having a sequence identity of at least 60% with the amino acid sequence of at least 35 contiguous amino acid residues from any one of SEQ ID NOs: 1-4, 6-11, 13-16, 18, 21-28, and 30,

said polypeptide being antigenic in a mammal.

8. The method according to claim 7 , wherein the animal receives between 0.5 and 5,000 μg of the polypeptide according to claim 1 per administration.

9. The method according to claim 7 , wherein the animal receives a priming administration and one or more booster administrations of said polypeptide or pharmaceutical composition.

10. The method according to claim 7 , wherein the animal is a human being.

11. The method according to claim 7 , wherein the adaptive immunity is effective in reducing the risk of contracting infection with C. jejuni or is effective in treating or ameliorating infection with C. jejuni.

12. The method according to claim 7 , wherein the administration is for the purpose of inducing antibodies specific for C. jejuni and wherein said antibodies or B-lymphocytes producing said antibodies are subsequently recovered from the animal.

13. The method according to claim 7 , wherein the administration is for the purpose of inducing antibodies specific for C. jejuni and wherein B-lymphocytes producing said antibodies are subsequently recovered from the animal and used for preparation of monoclonal antibodies.

Assignments (2)
CHANGE OF NAME Recorded Jan 10, 2018
From: EVAXION BIOTECH APS
To: EVAXION BIOTECH APS
Reel/Frame 045040/0366 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 26, 2016
From: MOLLER, NIELS IVERSON; MATTSSON, ANDREAS HOLM
To: EVAXION BIOTECH APS
Reel/Frame 037581/0328 →
Priority Claims (1)
DK 2011 00789 · Oct 12, 2011 · national
Continuity (2)
Provisional Application 61550494 · Oct 24, 2011
Related Publication 20140255416A1 · Sep 11, 2014