US2005106162A1PendingUtilityA1
Immunisation against chlamydia trachomatis
Priority: Dec 12, 2001Filed: Dec 12, 2002Published: May 19, 2005
Est. expiryDec 12, 2021(expired)· nominal 20-yr term from priority
A61P 31/10A61P 31/04A61P 15/00A61K 39/118A61K 39/00
52
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Claims
Abstract
The published genomic sequence of Chlamydia trachomatis reveals over 1000 putative encoded proteins but does not itself indicate which of these might be useful antigens for immunisation and vaccination or for diagnosis. This difficulty is addressed by the invention, which provides a number of C.trachomatis protein sequences suitable for vaccine production and development and/or for diagnosis purposes.
Claims
exact text as granted — not AI-modified1 - 12 . (canceled)
13 . A medicament for the treatment or prevention of an infection due to Chlamydia trachomatis comprising a protein, wherein the protein is selected from the group consisting of:
(a) a protein comprising an amino acid sequence selected from the group consisting of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37, 39, 41, 43, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73, 75, 77, 79, 81, 83, 85, 87, 89, 91, 93, 95, 97, 99, 101, 103, 105, 107, 109, 111, 113, 115, 117, 119, 121, 123, 125, 127, 129, 131, 133, 135, 137, 139, 141, 143, 145, 147, 149, 151, 153, 155, 157, 159, 161, 163, 165, 167, 169, 171, 173, 175, 177, 179, 181, 183, 185, 187, 189, 191, 193, 195, 197, 199, 201, 203, 205, 207, 209, 211, 213, 215, 217, 219, 221, 223, 225, 227, 229, 231, 233, 235, 237, 239, 241, 243, 245, 247, 249, 251, 253, 255, 257, 259, and 261; (b) a protein comprising an amino acid sequence having 50% or greater sequence identity to the amino acid sequence of (a); and (c) a protein comprising a fragment of at least 7 consecutive amino acids from the amino acid sequence of (a):
14 . A medicament for the treatment or prevention of an infection due to Chlamydia trachomatis comprising a nucleic acid, wherein the nucleic acid is selected from the group consisting of:
(a) a nucleic acid comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 98, 100, 102, 104, 106, 108, 110, 112, 114, 116, 118, 120, 122, 124, 126, 128, 130, 132, 134, 136, 138, 140, 142, 144, 146, 148, 150, 152, 154, 156, 158, 160, 162, 164, 166, 168, 170, 172, 174, 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232, 234, 236, 238, 240, 242, 244, 246, 248, 250, 252, 254, 256, 258, 260, and 262; (b) a nucleic acid comprising a nucleotide sequence having 50% or greater sequence identity to the nucleotide sequence of (a); and (c) a nucleic acid comprising a fragment of at least 7 consecutive nucleotides from the nucleotide sequence of (a).
15 . The medicament of claims 13 or 14 , wherein the infection is treated or prevented by the medicament eliciting an immune response which is specific to a Chlamydia elementary body.
16 . The medicament of claim 13 or 14 , wherein the medicament neutralizes Chlamydia trachomatis elementary bodies.
17 . An immunogenic composition comprising a protein, wherein the protein is selected from the group consisting of:
(a) a protein comprising an amino acid sequence selected from the group consisting of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37, 39, 41, 43, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73, 75, 77, 79, 81, 83, 85, 87, 89, 91, 93, 95, 97, 99, 101, 103, 105, 107, 109, 111, 113, 115, 117, 119, 121, 123, 125, 127, 129, 131, 133, 135, 137, 139, 141, 143, 145, 147, 149, 151, 153, 155, 157, 159, 161, 163, 165, 167, 169, 171, 173, 175, 177, 179, 181, 183, 185, 187, 189, 191, 193, 195, 197, 199, 201, 203, 205, 207, 209, 211, 213, 215, 217, 219, 221, 223, 225, 227, 229, 231, 233, 235, 237, 239, 241, 243, 245, 247, 249, 251, 253, 255, 257, 259, and 261; (b) a protein comprising an amino acid sequence having 50% or greater sequence identity to the amino acid sequence of (a); and (c) a protein comprising a fragment of at least 7 consecutive amino acids from the amino acid sequence of (a).
18 . An immunogenic composition comprising a nucleic acid, wherein the nucleic acid is selected from the group consisting of:
(a) a nucleic acid comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 98, 100, 102, 104, 106, 108, 110, 112, 114, 116, 118, 120, 122, 124, 126, 128, 130, 132, 134, 136, 138, 140, 142, 144, 146, 148, 150, 152, 154, 156, 158, 160, 162, 164, 166, 168, 170, 172, 174, 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232, 234, 236, 238, 240, 242, 244, 246, 248, 250, 252, 254, 256, 258, 260, and 262; (b) a nucleic acid comprising a nucleotide sequence having 50% or greater sequence identity to the nucleotide sequence of (a); and (c) a nucleic acid comprising a fragment of at least 7 consecutive nucleotides from the nucleotide sequence of (a).
19 . A method of neutralizing Chlamydia trachomatis infectivity in a patient comprising the step of administering to the patient the immunogenic composition of claim 17 , the immunogenic composition of claim 18 , or an antibody preparation which recognizes the medicament of claim 1 .
20 . A method of immunizing a patient against Chlamydia trachomatis comprising the step of administering to the patient the immunogenic composition of claim 17 or the immunogenic composition of claim 18 .
21 . A method of raising antibodies specific for Chlamydia trachomatis elementary bodies comprising the step of administering to the patient the immunogenic composition of claim 17 or the immunogenic composition of claim 18 .
22 . A method of raising antibodies which recognize the medicament of claim 1 comprising the step of administering to a patient the immunogenic composition of claim 17 or the immunogenic composition of claim 18 .
23 . A method for detecting a Chlamydia trachomatis elementary body in a biological sample comprising the step of contacting the sample with an antibody which recognizes the medicament of claim 1 .Join the waitlist — get patent alerts
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