US2020354412A1PendingUtilityA1

Anti-cancer dna vaccine employing plasmids encoding signal sequence, mutant oncoprotein antigen, and heat shock protein

Assignee: UNIV JOHNS HOPKINSPriority: May 5, 2003Filed: May 2, 2019Published: Nov 12, 2020
Est. expiryMay 5, 2023(expired)· nominal 20-yr term from priority
A61K 39/0011A61K 2039/585C12N 2710/20022C07K 2319/02C07K 14/35C12N 2710/20034A61K 2039/53A61K 2039/6043A61K 2039/54A61K 39/12A61P 35/00A61K 2039/55516
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Claims

Abstract

Novel nucleic acid vectors comprising sequences encoding (a) an antigen, (b) a signal peptide, and (c) a heat shock protein, are disclosed, as are methods for using such vectors to induce antigen-specific immune responses and to treat tumors.

Claims

exact text as granted — not AI-modified
1 . A nucleic acid molecule encoding a fusion polypeptide useful as a vaccine composition, which molecule comprises:
 (a) a first nucleic acid sequence encoding a first polypeptide or peptide that promotes processing via the MHC class I pathway;   (b) fused in frame with the first nucleic acid sequence, a second nucleic acid sequence encoding a signal peptide; and   (c) a third nucleic acid sequence that is linked in frame to said first nucleic acid sequence and that encodes an antigenic polypeptide or peptide.   
     
     
         2 . The nucleic acid molecule of  claim 1 , wherein the antigenic peptide comprises an epitope that binds to a MHC class I protein. 
     
     
         3 . The nucleic acid molecule of  claim 1  wherein the first polypeptide or peptide is Hsp70, an active C-terminal domain thereof, or a functional derivative of Hsp70 or of said C-terminal domain. 
     
     
         4 . The nucleic acid molecule of  claim 1 , wherein the first polypeptide is encoded by SEQ ID NO:9 or a fragment thereof that encodes a functional derivative of said polypeptide or the full length sequence of Hsp70 as set forth in GENBANK Z95324 AL123456 and encoded by nucleotides 10633-12510 of the  Mycobacterium tuberculosis  genome. 
     
     
         5 . The nucleic acid molecule of  claim 1 , wherein the first polypeptide is SEQ ID NO: 10 of functional derivative thereof. 
     
     
         6 . The nucleic acid molecule of  claim 1  wherein the antigen is one which is present on, or/cross-reactive with an epitope of, a pathogenic organism, cell, or virus. 
     
     
         7 . The nucleic acid molecule of  claim 6 , wherein the virus is a human papilloma virus. 
     
     
         8 . The nucleic acid molecule of  claim 7 , wherein the antigen is an E7 polypeptide of HPV-16 having the sequence SEQ ID NO: 2, or an antigenic fragment thereof. 
     
     
         9 . The nucleic acid molecule of  claim 8 , wherein the HPV-16 E7 polypeptide is a non-oncogenic mutant or variant of said E7 polypeptide. 
     
     
         10 . The nononcogenic mutant of  claim 9  wherein the sequence of the E7 polypeptide differs from SEQ ID NO: 2 by one or more of the following substitutions:
 (a) Cys at position 24 to Gly or Ala 
 (b) Glu at position 26 to Gly or Ala 
 (c) Cys at position 91 to Gly or Ala. 
 
     
     
         11 - 13 . (canceled) 
     
     
         14 . The nucleic acid molecule of  claim 1  that is characterized as pNG′VL4a-Sig/E7(detox)/HSP70, and has the sequence SEQ ID NO:13. 
     
     
         15 - 19 . (canceled) 
     
     
         20 . A pharmaceutical composition capable of inducing or enhancing an antigen-specific immune response, comprising:
 (a) pharmaceutically and immunologically acceptable excipient in combination with;   (b) a composition comprising the nucleic acid molecule of  claim 1 .   
     
     
         21 . A pharmaceutical composition capable of inducing or enhancing an antigen-specific immune response, comprising:
 (a) pharmaceutically and immunologically acceptable excipient in combination with;   (b) the nucleic acid molecule of  claim 14 .   
     
     
         22 - 23 . (canceled) 
     
     
         24 . A method of inducing or enhancing an antigen specific immune response in a subject comprising administering to the subject an effective amount of the pharmaceutical composition of  claim 20 , thereby inducing or enhancing said response. 
     
     
         25 - 26 . (canceled) 
     
     
         27 . The method of  claim 24 , wherein the response is mediated at least in part by CD8 +  cytotoxic T lymphocytes (CTL). 
     
     
         28 - 36 . (canceled) 
     
     
         37 . A method of inhibiting growth or preventing re-growth of a tumor expressing HPV E7 or E6 protein in a subject, comprising administering to said subject an effective amount of a pharmaceutical composition of  claim 20 , wherein said third nucleic acid sequence encodes one or more epitopes of E7 or E6, thereby inhibiting said growth or preventing said re-growth. 
     
     
         38 . A method of inhibiting growth or preventing re-growth of a tumor expressing HPV E7 or E6 protein in a subject, comprising administering to said subject an effective amount of a pharmaceutical composition of  claim 21 , wherein said third nucleic acid sequence encodes one or more epitopes of E7 or E6, thereby inhibiting said growth or preventing said re-growth. 
     
     
         39 - 40 . (canceled)

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