US2009269349A1PendingUtilityA1
Antigenic polypeptides
Est. expiryAug 2, 2021(expired)· nominal 20-yr term from priority
A61P 39/02A61P 37/04A61P 9/00A61P 31/04A61P 31/06A61P 27/02A61P 11/00A61P 1/04A61K 2039/505C07K 14/31A61P 11/02C07K 16/00C07K 16/12C07K 16/30A61K 39/00Y02A50/30
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Claims
Abstract
The invention relates to a method for the identification of antigenic polypeptides, typically opsonic antigens, expressed by pathogenic microbes; vaccines comprising said antigens; and therapeutic antibodies directed to said antigenic polypeptides.
Claims
exact text as granted — not AI-modified1 . An antigenic polypeptide, or part thereof, encoded by an isolated DNA molecule selected from the group consisting of:
(i) a DNA molecule of SEQ ID NO.: 57; (ii) a DNA molecule which hybridizes to the DNA molecule identified in (i) which encodes a polypeptide expressed by a pathogenic organism; and (iii) a DNA molecule which is 85% or more homologous to the DNA sequence defined in (i) or (ii).
2 . An antigenic polypeptide according to claim 1 , wherein said polypeptide is represented by the amino acid sequence of SEQ ID NO.: 244.
3 . An antigenic polypeptide according to claim 1 wherein said polypeptide is derived from a bacterium selected from the group consisting of Staphylococcus sp.; Enterococcus faecalis; Mycobacterium tuberculsis; Streptococcus group B; Streptococcus pneumoniae; Helicobacter pylori; Neisseria gonorrhea; Streptococcus group A; Borrelia burgdorferi; Coccidiodes immitis; Histoplasma sapsulatum; Neisseria meningitides type B; Shigella flexneri; Escherichia coli ; and Haemophilus influenza.
4 . An antigenic polypeptide according to claim 4 wherein the Staphylococcus sp is Staphylococcus aureus or Staphylococcus epidermidis.
5 . An antigenic polypeptide according to claim 1 , wherein said DNA molecule hybridizes to sequence of SEQ ID NO.: 57 under stringent hybridization conditions.
6 . An antigenic polypeptide according to claim 1 wherein said DNA molecule is genomic DNA.
7 . A method of generating an immune response in an animal against a pathogenic microbe, the method comprising administering to said animal a polypeptide of SEQ ID NO.: 244.
8 . A method according to claim 7 , wherein said animal is human.
9 . A method according to claim 7 , further comprising a polypeptide of SEQ ID NO. 127.
10 . A method according to claim 7 , further comprising one or more polypeptides selected from the group consisting of SEQ ID. NOs. 123-126, 128-243, and 245-424.
11 . A method according to claim 7 , wherein said pathogenic microbe comprises Staphylococcus aureus.
12 . An antibody against an antigenic polypeptide of claim 1 .
13 . An antibody according to claim 12 , wherein said antibody is a monoclonal antibody.
14 . An antibody according to claim 12 , wherein said antibody is a chimeric antibody.
15 . An antibody according to claim 12 , wherein said antibody is a humanized antibody.
16 . An antibody according to claim 12 , wherein said antibody is an opsonic antibody.
17 . A method for preparing a hybridoma cell-line producing an antibody, the method comprising the steps of:
i) immunizing an immunocompetent mammal with an immunogenic comprising at least one polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NOS.: 123-424, or an antigenic fragment thereof; ii) fusing lymphocytes of the immunized immunocompetent mammal with myeloma cells to form hybridoma cells; iii) culturing the hybridoma cells to proliferate and to secrete said monoclonal antibody; iv) screening monoclonal antibodies produced by the hybridoma cells of step (ii) for binding activity to the amino acid sequences of (i).
18 . A method according to 17 , further comprising: recovering the antibody.
19 . A method according to claim 17 , wherein said hybridoma cell-line produces opsonic antibodies.Cited by (0)
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