US2005074459A1PendingUtilityA1
Escherichia coli O157:H7 epithelial adhesin
Assignee: CHILDREN S HOSPITAL & REGIONALPriority: Jun 24, 1994Filed: Jul 23, 2003Published: Apr 7, 2005
Est. expiryJun 24, 2014(expired)· nominal 20-yr term from priority
A61K 39/00C12R 2001/19C12N 1/205Y10S530/825A61K 38/00C07K 14/245
55
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Claims
Abstract
Polypeptides encoded by a continuous segment of chromosomal DNA from E. coli O157:H7, isolated on plasmid pSC(overlap)(ATCC No. 69648), that encodes an adhesin (SEQ ID NO:5) that mediates bacterial colonization of bovine intestines, vaccines derived therefrom, and antibodies directed against the adhesin are disclosed.
Claims
exact text as granted — not AI-modified1 - 6 . (canceled)
7 . A vaccine formulation for preventing and/or treating infection by a pathogenic member of the family Enterobacteriaceae in a mammalian subject comprising a peptide encoded by a nucleic acid molecule that hybridizes under stringent conditions to a nucleic acid molecule selected from the group of the nucleotide sequence of SEQ ID NO:4 and the nucleotide sequence complementary to SEQ ID NO:4, and a pharmaceutically acceptable carrier.
8 . The vaccine formulation of claim 7 wherein the pharmaceutically acceptable carrier is suitable for administration by a route selected from the group consisting of an oral route, an intranasal route and a parenteral route.
9 . The vaccine formulation of claim 7 wherein the pharmaceutically acceptable carrier is selected from the group consisting of sesame oil, peanut oil, sterile aqueous solution, and isotonic solutions suitable for injection.
10 . The vaccine formulation of claim 7 wherein said pharmaceutically acceptable carrier comprises liposomes.
11 . The vaccine formulation of claim 8 wherein said vaccine formulation is packaged in enteric coated capsules.
12 . The vaccine formulation of claim 7 which further comprises a stabilizer.
13 . The vaccine formulation of claim 12 wherein the stabilizer is selected from the group consisting of sorbitol and gelatin.
14 . The vaccine formulation of claim 7 which further comprises an immunoadjuvant.
15 . The vaccine formulation of claim 14 wherein the immunoadjuvant is selected from the group consisting of: the water-in-oil emulsion of Freund, light mineral oil, Arlacel A, Arlacel C, liposome-antigen combinations, cholera toxin B subunit conjugates and monophosphoryl lipid A.
16 . The vaccine formulation of claim 7 which comprises a peptide that is encoded by a nucleic acid molecule that hybridizes under stringent conditions to the nucleotide sequence of SEQ ID NO:4 or its complement.
17 . The vaccine formulation of claim 16 wherein said peptide is derived from a recombinant organism.
18 . The vaccine formulation of claim 16 wherein said peptide is produced in a transgenic plant.
19 . The vaccine formulation of claim 16 which comprises an amount of the peptide effective to promote the clearance of the pathogenic enterobacteriaceae from the gastrointestinal tract of a mammalian subject infected by a pathogenic member of the family Enterobacteriaceae when administered thereto.Join the waitlist — get patent alerts
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