IP Library › Granted Patent US 11,572,391
Granted Patent B2
US 11,572,391 · App. 17/098,021 · Granted Feb 7, 2023

Antibodies for prevention, treatment and diagnosis of

Inventors: Eric Charles Reynolds (Melbourne, AU); Neil Martin O'Brien Simpson (Melbourne, AU); Keith J. Cross (Melbourne, AU); Nada Slakeski (Melbourne, AU)
Assignee: Oral Health Australia PTY Ltd
C07K14/195A61K39/0216C07K16/1203C07K16/1257C12N9/14C12N9/52C12Y304/21G01N33/56955A61K2039/505A61K2039/53A61K2039/55566C07K2317/34C07K2317/76C07K2319/00C12Y304/21004C12Y306/05002G01N2333/95
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Quick Facts
Patent No.
US 11,572,391
App. No.
17/098,021
Granted
Feb 7, 2023
Kind
B2
Abstract

Disclosed are P. gingivalis antibodies raised against a chimeric or fusion protein, wherein the chimeric or fusion protein comprises a first peptide joined directly or through a linker to a second peptide or polypeptide, wherein (A) the first peptide comprises a region of a P. gingivalis trypsin-like enzyme and (B) the second peptide or polypeptide comprises an adhesin domain of P. gingivalis.

Claims (15)

1. An isolated antibody raised against a chimeric or fusion protein, wherein the chimeric or fusion protein comprises a first peptide joined directly or through a linker to a second peptide or polypeptide, wherein:

(A) said first peptide comprises a region of a Porphyromonas gingivalis trypsin-like enzyme selected from the group consisting of the amino acid sequence that is the same as, or at least 90% homologous to, the sequence shown in any one of SEQ ID NOs: 1-34; and

(B) said second peptide or polypeptide comprises P. gingivalis adhesin domain sequence selected from the group consisting of the amino acid sequence that is the same as, or at least 90% homologous to, the sequence shown in any one of SEQ ID NOs: 35-39;

Wherein the antibody is obtained by a process comprising immunizing a non-human animal with the chimeric or fusion protein, and isolating and purifying the antibody from the non-human animal.

2. The antibody according to claim 1 , wherein the antibody is a monoclonal antibody.

3. A method for the diagnosis or monitoring of a P. gingivalis -related condition or disease in a subject, comprising assaying a biological sample from said subject with the antibody according to claim 1 , to detect the presence of P. gingivalis.

4. The antibody according to claim 1 , wherein said first peptide comprises a sequence selected from the group consisting of SEQ ID NOs: 3-34 and sequences at least 90% homologous thereto.

5. The antibody according to claim 4 , wherein said second peptide or polypeptide comprises a sequence selected from the group consisting of SEQ ID NOs: 35-39 and sequences at least 90% homologous thereto.

6. The antibody according to claim 1 , wherein said first peptide comprises a sequence that is the same as or at least 90% homologous to a sequence selected from the group consisting of SEQ ID NOs: 31-34 and said second peptide or polypeptide comprises a sequence that is the same as or at least 90% homologous to SEQ ID NO: 39.

7. The antibody according to claim 1 , wherein:

the C-terminal residue of said first peptide is covalently linked directly or through a linker that is either (i) up to 15 amino acids in length, or (ii) less than 5 amino acids in length, to either (a) the N-terminal residue of said second peptide or polypeptide or (b) the C-terminal residue of said second peptide or polypeptide, or

the N-terminal residue of said first peptide is covalently linked directly or through a linker that is either (i) up to 15 amino acids in length, or (ii) less than 5 amino acids in length, to either (a) the N-terminal residue of said second peptide or polypeptide or (b) the C-terminal residue of said second peptide or polypeptide.

8. The antibody according to claim 1 , wherein the first peptide comprises a sequence selected from the group consisting of SEQ ID Nos: 27-30 and sequences at least 90% homologous thereto, and said second polypeptide comprises a sequence selected from SEQ ID NO: 36-37 and sequences at least 90% homologous thereto.

9. The antibody according to claim 1 , wherein said first peptide comprises a sequence that is the same as or is at least 90% identical to the sequence of SEQ ID NO: 28 and said second peptide or polypeptide comprises a sequences that is the same or is at least 90% identical to the sequence of SEQ ID NO: 37.

10. The antibody according to claim 1 , wherein said first peptide comprises a sequence that is the same as or is at least 90% identical to the sequence of SEQ ID NO: 27 and said second peptide or polypeptide comprises a sequences that is the same or is at least 90% identical to the sequence of SEQ ID NO: 36.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2023
From: REYNOLDS, ERIC CHARLES; O'BRIEN SIMPSON, NEIL MARTIN; CROSS, KEITH J; SLAKESKI, NADA
To: ORAL HEALTH AUSTRALIA PTY LTD
Reel/Frame 062270/0477 →
Priority Claims (3)
AU 2008904476 · Aug 29, 2008 · national
AU 2008905483 · Oct 23, 2008 · national
AU 2009903052 · Jun 30, 2009 · national
Continuity (6)
Continuation 16134721 · Sep 18, 2018
Continuation 15370144 · Dec 6, 2016
Continuation 14487461 · Sep 16, 2014
Division 13060653
Provisional Application 61151132 · Feb 9, 2009
Related Publication 20210079047A1 · Mar 18, 2021