Proteins and nucleic acids useful in vaccines targeting
Disclosed are novel immunogenic proteins derived from Staphylococcus aureus , as well as methods for their use in conferring protective immunity against S. aureus infections. Also disclosed are nucleic acids encoding the proteins and methods of use of these nucleic acids.
1. A pharmaceutical composition comprising, a polypeptide comprising: a) an amino acid sequence consisting of SEQ ID NO: 18, or b) an amino acid sequence consisting of at least 35 contiguous amino acid residues from SEQ ID NO: 18, or c) an amino acid sequence having a sequence identity of at least 95% with the amino acid sequence of a), or d) an amino acid sequence having a sequence identity of at least 95% with the amino acid sequence of b), or said polypeptide being antigenic in a mammal, and an immunological adjuvant and a pharmaceutically acceptable carrier, vehicle or diluent.
2. The pharmaceutical composition according to claim 1 , wherein the adjuvant is an aluminium based adjuvant.
3. The pharmaceutical composition according to claim 1 , wherein the sequence identity defined in c) or d) is at least 95%, at least 96%, at least 97%, at least 98%, and at least 99%.
4. The pharmaceutical composition according to claim 1 , wherein the at least 35 contiguous amino acid residues of option b) has an N-terminal amino acid residue corresponding to any one of amino acid residues 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, 47, 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, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, and 370 in SEQ ID NO: 18,
wherein the N-terminal first residue will not be higher numbered than 405-L, where L is the number of amino acids defined for option b.
5. The pharmaceutical composition according to claim 1 , wherein the polypeptide is fused or conjugated to an immunogenic carrier molecule.
6. The pharmaceutical composition according to claim 1 , wherein the immunogenic carrier molecule is a polypeptide that induces T-helper lymphocyte responses in a majority of humans, such as an immunogenic carrier protein selected from the group consisting of keyhole limpet hemocyanin or a fragment thereof, tetanus toxoid or a fragment thereof, diphtheria toxoid or a fragment thereof.
7. The pharmaceutical composition according to claim 1 , wherein the polypeptide is capable of inducing an adaptive protective immune response against infection with multi-resistant S. aureus in a mammal, in particular in a human being.
8. The pharmaceutical composition according to claim 7 , which induces a humoral and/or a cellular immune response.
9. A method for inducing immunity in an animal by administering at least once an immunogenically effective amount of a pharmaceutical composition according to claim 1 so as to induce adaptive immunity against S. aureus in the animal.
10. The method according to claim 9 , wherein, when the pharmaceutical composition comprising said polypeptide is administered, the animal receives between 0.5 and 5,000 μg of the polypeptide per administration.
11. The method according to claim 9 , wherein the animal receives a priming administration and one or more booster administrations.
12. The method according to claim 9 , wherein the animal is a human being.
13. The method according to claim 9 , wherein the administration is for the purpose of inducing protective immunity against S. aureus.
14. The method according to claim 13 , wherein the protective immunity is effective in reducing the risk of attracting infection with S. aureus or is effective in treating or ameliorating infection with S. aureus.