US2023374081A1PendingUtilityA1

Prevention, treatment and diagnosis of p.gingivalis infection

Assignee: ORAL HEALTH AUSTRALIA PTY LTDPriority: Aug 29, 2008Filed: Jan 9, 2023Published: Nov 23, 2023
Est. expiryAug 29, 2028(~2.1 yrs left)· nominal 20-yr term from priority
C07K 14/195A61K 39/0216G01N 33/56955C07K 16/1257C12N 9/14C12N 9/52C07K 16/1203C12Y 304/21A61K 2039/53C07K 19/00G01N 33/6854C07K 2319/00G01N 2469/20A61K 2039/55566C07K 2317/34C12Y 304/21004C12Y 306/05002A61P 1/02A61P 31/04A61P 43/00A61K 38/00A61K 39/02A61K 39/40C12N 15/09C12N 15/62C07K 2317/76A61K 2039/505G01N 2333/95
81
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The invention relates to generation and use of cellular and humoral responses for the prevention and treatment of P. gingivalis related conditions and diseases.

Claims

exact text as granted — not AI-modified
1 - 70 . (canceled) 
     
     
         71 . A chimeric or fusion protein for inducing an immune response to  P. gingivalis , the protein comprising 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  P. gingivalis  trypsin-like enzyme, wherein the first peptide comprises part of, or all of a sequence that is the same as, or at least 90% homologous to the sequence shown in any one of SEQ ID Nos: 1, 2, or 27 to 34; and   (B) said second peptide or polypeptide comprises a  P. gingivalis  adhesin domain sequence or fragment thereof, wherein the second peptide or polypeptide comprises part of, or all of a sequence that is the same as, or at least 90% homologous to the sequence shown in any one of SEQ ID Nos: 35 to 39.   
     
     
         72 . The chimeric or fusion protein according to  claim 71 , wherein said first peptide comprises a sequence selected from the group consisting of SEQ ID NOs: 27 to 34. 
     
     
         73 . The chimeric or fusion protein according to  claim 71 , wherein said second peptide or polypeptide comprises a sequence selected from the group consisting of SEQ ID NOs: 35 to 37. 
     
     
         74 . The chimeric or fusion protein according to  claim 71 , wherein:
 (a) 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: 27-30 and said second peptide or polypeptide comprises a sequence that is the same as or 90% homologous to a sequence selected from the group consisting of SEQ ID NOs: 36-37; or   (b) 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.   
     
     
         75 . The chimeric or fusion protein according to  claim 71 , wherein:
 (a) said first peptide comprises a sequence that is the same or at least 90% homologous to the sequence shown in SEQ ID NO: 28 and said second peptide or polypeptide comprises a sequence that is the same or at least 90% homologous to the sequence shown in SEQ ID NO: 37; or   (b) said first peptide comprises a sequence that is the same or at least 90% homologous to the sequence shown in SEQ ID NO: 27 and said second peptide or polypeptide comprises a sequence that is the same or at least 90% homologous to the sequence shown in SEQ ID NO: 36.   
     
     
         76 . A chimeric or fusion protein according to  claim 71 , 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 or (b) the C-terminal residue of said second peptide or polypeptide.   
     
     
         77 . A chimeric or fusion protein according to  claim 71 , wherein:
 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 or (b) the C-terminal residue of said second peptide or polypeptide.   
     
     
         78 . A composition comprising a chimeric or fusion protein according to  claim 71 . 
     
     
         79 . The composition according to  claim 78 , further comprising an adjuvant. 
     
     
         80 . A method of preventing or reducing the incidence or severity of a  P. gingivalis -related condition or disease in a subject, comprising administering to the subject a chimeric or fusion protein of  claim 71 . 
     
     
         81 . An antibody raised against the chimeric or fusion protein of  claim 71 . 
     
     
         82 . The antibody according to  claim 81 , wherein the antibody is a monoclonal antibody. 
     
     
         83 . A method of preventing or reducing the severity of a  P. gingivalis -related disease or condition in a subject, comprising administering to the subject the antibody of  claim 71 . 
     
     
         84 . A nucleic acid molecule comprising a sequence encoding the chimeric or fusion protein of  claim 71 . 
     
     
         85 . A method for the diagnosis or monitoring of a  P. gingivalis -related condition or disease in a subject, which comprises assaying a biological sample from said subject with the chimeric or fusion protein of  claim 71  to detect anti- P. gingivalis  antibodies. 
     
     
         86 . A method for the diagnosis or monitoring of a  P. gingivalis -related condition or disease in a subject, which comprises assaying a biological sample from said subject with the antibody according to  claim 81 , to detect the presence of  P. gingivalis.

Join the waitlist — get patent alerts

Track US2023374081A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.