Porphyromonas gingivalis polypeptides
Provided herein are compositions and methods for eliciting an immune response against Porphyromonas gingivalis . The compositions and methods relate to P. gingivalis polypeptides and fragments and variants thereof and the corresponding polynucleotides which are useful in the diagnosis, prevention and therapy of P. gingivalis infections (e.g. periodontitis). Antibodies against the polypeptides and compositions and methods including these antibodies are also disclosed. The disclosure also describes methods for the detection, prevention and treatment of P. gingivalis infection (e.g. periodontitis).
1. An immunogenic composition comprising at least one isolated polypeptide, an adjuvant that induces a Th2-biased immune response, and a pharmaceutically acceptable carrier, wherein the at least one polypeptide is selected from the group consisting of Porphyromonas gingivalis protein PG2172 (SEQ ID NO. 3), a polypeptide having at least 80% identity to SEQ ID NO. 3, an immunogenic fragment of 8, 9, 10, 12, 13, 16, 18, 20, 25, 30, 35, 40, 50, 60, 70, 80, 90, 100, 150, 200 or more consecutive amino acids of SEQ ID NO. 3, and a variant comprising a conservative substitution of at least one amino acid of SEQ ID NO. 3.
2. An immunogenic composition comprising at least one isolated polypeptide having at least 80% identity to SEQ ID NO. 3, an adjuvant that induces a Th2-biased immune response, and a pharmaceutically acceptable carrier.
3. The immunogenic composition of claim 1 or 2 wherein the adjuvant is an aluminum salt adjuvant.
4. The immunogenic composition of claim 3 wherein the aluminum salt adjuvant is an aluminum hydroxide or aluminum phosphate.
5. The immunogenic composition of claim 4 wherein the aluminum salt adjuvant is an aluminum hydroxide.
6. The immunogenic composition of claim 2 wherein the immunogenic composition is formulated for use orally.
7. The immunogenic composition of claim 2 wherein the immunogenic composition is formulated for percutaneous administration.
8. The immunogenic composition of claim 2 wherein the immunogenic composition is in a kit form comprising the composition and instructions for use.
9. P. gingivalis protein PG2172 (SEQ ID NO. 3), or an immunogenic fragment consisting of 8, 9, 10, 12, 13, 16, 18, 20, 25, 30, 35, 40, 50, 60, 70, 80, 90, 100, 150, 200 or more consecutive amino acids of SEQ ID NO. 3, or a variant comprising a conservative substitution of at least one amino acid of SEQ ID NO. 3, immobilized on a solid support or solid matrix.
10. A polypeptide having at least 80% identity to SEQ ID NO. 3 immobilized on a solid support or solid matrix.
11. An immunogenic composition comprising at least one isolated polypeptide and a pharmaceutically acceptable carrier, wherein the at least one polypeptide consists of the amino acid sequence as set out in SEQ ID NO: 29.
12. The immunogenic composition of claim 11 further comprising an adjuvant.
13. The immunogenic composition of claim 12 wherein the adjuvant is an aluminum salt adjuvant.
14. The immunogenic composition of claim 13 wherein the aluminum salt adjuvant is an aluminum hydroxide or aluminum phosphate.
15. The immunogenic composition of claim 14 wherein the aluminum salt adjuvant is an aluminum hydroxide.