US2007149474A1PendingUtilityA1
Methods and compositions for vaccination comprising nucleic acid and/or polypeptide sequences of chlamydia
Est. expiryDec 15, 2020(expired)· nominal 20-yr term from priority
A61K 2039/53A61P 31/04A61P 37/04A61K 39/118
64
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Claims
Abstract
The instant invention relates to antigens and nucleic acids encoding such antigens obtainable by screening a Chlamydia genome. In more specific aspects, the invention relates to methods of isolating such antigens and nucleic acids and to methods of using such isolated antigens for producing immune responses. The ability of an antigen to produce an immune response may be employed in vaccination or antibody preparation techniques.
Claims
exact text as granted — not AI-modified1 . A vaccine comprising:
(a) a pharmaceutically acceptable carrier, and (b) at least one polynucleotide having a Chlamydia sequence.
2 . The vaccine of claim 1 , wherein the at least one polynucleotide has a Chlamydia psittaci sequence.
3 . The vaccine of claim 1 , wherein the at least one polynucleotide has a Chlamydia pneumoniae sequence.
4 . The vaccine of claim 1 , wherein the at least one polynucleotide has a sequence isolated from a Chlamydia psittaci genomic DNA expression library.
5 . The vaccine of claim 4 , wherein the at least one polynucleotide has a sequence isolated from a Chlamydia psittaci genomic DNA expression library.
6 . The vaccine of claim 1 , wherein the at least one polynucleotide has a sequence of SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, SEQ ID NO: 38, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID NO: 50, SEQ ID NO: 52, SEQ ID NO: 54, SEQ ID NO: 56, SEQ ID NO: 58, SEQ ID NO: 60, or fragment thereof.
7 . The vaccine of claim 6 , wherein the at least one polynucleiotide has a sequence of SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:12, SEQ ID NO:14, SEQ ID NO:16, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, or SEQ ID NO:26, or fragment thereof.
8 . The vaccine of claim 6 , wherein the at least one polynucleotide has a sequence of SEQ ID NO:6, SEQ ID NO:10, SEQ ID NO:14, SEQ ID NO:20, or SEQ ID NO:24, or fragment thereof.
9 . The vaccine of claim 1 , wherein at least one polynucleotide has a sequence of SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, or SEQ ID NO:68 or fragment thereof.
10 . The vaccine of claim 1 , comprising a polynucleotide encoding an antigen having a sequence of SEQ ID NO:7, SEQ ID NO:7, SEQ ID NO:11, SEQ ID NO:13, SEQ ID NO:15, SEQ ID NO:17, SEQ ID NO:19, SEQ ID NO:21, SEQ ID NO:23, or SEQ ID NO:25, SEQ ID NO:27, SEQ ID NO:29, SEQ ID NO:31, SEQ ID NO:33, SEQ ID NO:35, SEQ ID NO:37, SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, or SEQ ID NO:45, SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:51, SEQ ID NO:53, SEQ ID NO:55, SEQ ID NO:57, SEQ ID NO:59, SEQ ID NO:61, or an antigenic fragment thereof.
11 . The vaccine of claim 1 , comprising a polynucleotide encoding an antigen having a sequence of SEQ ID NO:63, SEQ ID NO:65, SEQ ID NO:67, or SEQ ID NO:69, or an antigenic fragment thereof.
12 . The vaccine of claim 1 , wherein the polynucleotide is comprised in generic immunization vector.
13 . The vaccine of claim 12 , wherein the vector comprises a gene encoding a mouse ubiquitin fusion polypeptide.
14 . The vaccine of claim 12 , wherein the vector comprises a promoter operable in eukaryotic cells.
15 . The vaccine of claim 14 , wherein the promoter is a CMV promoter.
16 . The vaccine of claim 1 , wherein the polynucleotide is cloned into a viral expression vector.
17 . The vaccine of claim 16 , wherein the viral expression is selected form the group consisting of adenvirus, adeno-associated virus, retrovirus and herpes-simplex virus.
18 . The vaccine of claim 1 , comprising at least a first polynucleotide having a Chlamydia psittaci sequence and a second polynucleotide having a sequence, wherein the first polynucleotide and the second polynucleotide have different sequences.
19 . The vaccine of claim 6 , wherein the first polynucleotide has a sequence of SEQ ID NO: 50.
20 . A vaccine comprising:
(a) a pharmaceutically acceptable carrier; and (b) at least one Chlamydia antigen.
21 . The vaccine of claim 20 , wherein the at least one Chlamydia antigen has a sequence of SEQ ID NO:7, SEQ ID NO:9, SEQ ID NO:11, SEQ ID NO:13, SEQ ID NO. 15, SEQ ID NO:17, SEQ ID NO:19, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:27, SEQ ID NO:29, SEQ ID NO:31, SEQ ID NO:33, SEQ ID NO:35, SEQ ID NO:37, SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:51, SEQ ID NO:53, SEQ ID NO:55, SEQ ID NO:57, SEQ ID NO:59, or SEQ ID NO:61, or an antigenic fragment thereof.
22 . The vaccine of claim 20 , where the at least one Chlamydia antigen has a sequence of SEQ ID NO:7, SEQ ID NO:9, SEQ ID NO:11, SEQ ID NO:13, SEQ ID NO. 15, SEQ ID NO:17, SEQ ID NO:19, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, or SEQ ID NO:27, or an antigenic fragment thereof.
23 . The vaccine of claim 20 , wherein the at least one Chlamydia antigen has a sequence of SEQ ID NO:7, SEQ ID NO:11, SEQ ID NO.15, SEQ ID NO:21, or SEQ ID NO:25, or an antigenic fragment thereof.
24 . The vaccine of claim 20 , wherein the at least one Chlamydia antigen has a sequence of SEQ ID NO:63, SEQ ID NO:65, SEG ID NO:67, or SEQ ID NO:69, or an antigenic fragment thereof.
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