US2011129475A1PendingUtilityA1
Basb 205 polypeptides and polynucleotides from haemophilus influenzae
Est. expiryOct 13, 2020(expired)· nominal 20-yr term from priority
Inventors:Joelle Thonnard
A61P 31/04C07K 14/285
43
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Claims
Abstract
The invention provides BASB205 polypeptides and polynucleotides encoding BASB205 polypeptides and methods for producing such polypeptides by recombinant techniques. Also provided are diagnostic, prophylactic and therapeutic uses.
Claims
exact text as granted — not AI-modified1 . An isolated polypeptide comprising an amino acid sequence selected from:
(a) the amino acid sequence selected from SEQ ID NO:4, 6, 8 and 12; and (b) an amino acid sequence which has at least 99% identity to the amino acid sequence set forth in SEQ ID NO: 10, over the entire length of said sequence; and (c) the amino acid sequence set forth in SEQ ID NO:10.
2 . The isolated polypeptide of claim 1 , consisting of the amino acid sequence selected from SEQ ID NO: 4, 6, 8, 10 and 12.
3 . An immunogenic fragment of a polypeptide comprising an amino acid sequence which has at least 85% identity to the amino acid sequence selected from SEQ ID NO: 2, 4, 6, 8, 10 and 12, over the entire length of said sequence, wherein said fragment (if necessary when coupled to a carrier) is capable of raising an immune response which recognizes a polypeptide of SEQ ID NO: 4, 6, 8, 10 or 12.
4 . The isolated polypeptide of claim 1 , wherein said polypeptide is part of a larger fusion protein.
5 . An isolated polynucleotide encoding the polypeptide of claim 1 .
6 . An isolated polynucleotide comprising a nucleotide sequence complementary to the isolated polynucleotide of claim 5 .
7 . The isolated polynucleotide of claim 5 , comprising a nucleotide sequence selected from SEQ ID NO: 1, 3, 5, 7, 9, and 11; or a nucleotide sequence complementary to said isolated polynucleotide.
8 . An expression vector or a recombinant live microorganism comprising the isolated polynucleotide according to claim 5 .
9 . A host cell comprising the expression vector of claim 8 , or a subcellular fraction or a membrane of said host cell.
10 . A process for producing a polypeptide expressed by the host cell of claim 9 , comprising culturing the host cell under conditions sufficient for production of the polypeptide and recovering the polypeptide from the culture medium.
11 . A process for expressing the isolated polynucleotide of claim 5 comprising transforming a host cell with an expression vector comprising said polynucleotide and culturing said host cell under conditions sufficient for expression of said polynucleotide.
12 . An immunogenic composition comprising an effective amount of the immunogenic fragment of claim 3 , and a pharmaceutically acceptable carrier.
13 . An immunogenic composition comprising (a) a pharmaceutically acceptable carrier and (b)(i) an effective amount of the isolated polypeptide of claim 1 ; (ii) an effective amount of an immunogenic fragment of the isolated polypeptide of claim 1 ; or (iii) an effective amount of a polypeptide comprising an amino acid sequence at least 85% identical to the amino acid sequence set forth in SEQ ID NO:2, 4, 6, 8, 10, or 12.
14 . An immunogenic composition comprising an effective amount of the polynucleotide of claim 5 , and a pharmaceutically acceptable carrier.
15 . The immunogenic composition according to claim 12 , wherein said composition comprises at least one other non typeable Haemophilus influenzae antigen.
16 . An isolated antibody immunospecific for the polypeptide of claim 1 , or an immunological fragment of the isolated antibody.
17 . A method of diagnosing a non typeable Haemophilus influenzae infection, comprising identifying a polypeptide comprising an amino acid sequence which has at least 85% identity to the amino acid sequence selected from SEQ ID NO: 2, 4, 6, 8, 10 and 12, over the entire length of said sequence, or an antibody that is immunospecific for said polypeptide, present within a biological sample from an animal suspected of having a non typeable H. influenzae infection.
18 . A therapeutic composition for treating humans with non typeable Haemophilus influenzae disease comprising the isolated antibody of claim 16 and a suitable pharmaceutical carrier.
19 . A method of generating an immune response in an animal, comprising administering the immunogenic composition of claim 13 to the animal.
20 . A method of generating an immune response in an animal, comprising administering to the animal (a) the immunogenic composition of claim 14 ; or (b) an immunogenic composition comprising an immunologically effective amount of a polynucleotide comprising a nucleotide sequence which has at least 85% identity to the nucleotide sequence selected from SEQ ID NO: 1, 3, 5, 7, 9 and 11, over the entire length of said sequence.Join the waitlist — get patent alerts
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