US2015010595A1PendingUtilityA1
Vaccines comprising an immunostimulatory peptide and an immunostimulatory oligodeoxynucleic acid molecule
Est. expiryMar 24, 2023(expired)· nominal 20-yr term from priority
A61P 31/20A61P 31/04C12N 2730/10134A61P 31/16A61K 39/145A61K 39/29A61K 39/12C12N 7/00A61K 39/292A61K 2039/55505C12N 2770/24234C12N 2760/16122A61P 31/18A61K 39/39C12N 2760/16034A61P 31/00C12N 2730/10122A61K 2039/57C12N 2760/16222A61K 2039/55561C12N 2760/16234C07K 14/005A61K 2039/55516A61P 31/12C12N 2760/16134C12N 2770/24222A61K 39/00Y02A50/30
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Claims
Abstract
The invention refers to an improved vaccine against infections with pathogens, especially viral pathogens, comprising an antigen, a peptide of the formula R 1 —XZSZ N —XZX—R 2 and an immunostimulatory deoxynucleic acid containing deoxyinosine and/or deoxyuridine residues.
Claims
exact text as granted — not AI-modified1 - 16 . (canceled)
17 . A method of improving an antigen-specific type 1 response of a vaccine against a viral pathogen and preserving or increasing a type 2 response of said vaccine comprising:
obtaining a peptide comprising the sequence KLKL 5 KLK (SEQ ID NO: 6) and an I-ODN, wherein the I-ODN comprises oligo-d(IC) 13 (SEQ ID NO: 21); and administering the peptide and the I-ODN with a vaccine against a viral pathogen to a subject;
wherein the antigen-specific type 1 response to the vaccine against a viral pathogen is improved in the subject and the type 2 response to the vaccine is preserved or increased in the subject.
18 . The method according to claim 17 wherein the antigen-specific type 1 response is further defined as an IgG2-antibody response or an IFN-gamma response.
19 . The method according to claim 17 wherein the type 2 response is further defined as an IgG1-antibody response or an interleukin-4 (IL-4) response.
20 . The method according to claim 17 wherein the vaccine comprises a viral antigen.
21 . The method according to claim 17 wherein the vaccine further comprises an Al(OH)3 adjuvant.
22 . The method according to claim 20 wherein the viral antigen is derived from HIV, HAV, HBV, HCV, JEV, RSV, EBV, Influenza virus, HPV or Rotavirus.
23 . The method according to claim 17 wherein the vaccine further comprises a polycationic peptide.
24 . The method according to claim 17 wherein the vaccine further comprises an oligodeoxynucleotide containing a CpG-motif.
25 . The method according to claim 17 wherein the vaccine further comprises a polycationic peptide and an oligodeoxynucleotide containing a CpG-motif.
26 . A method of improving an antigen-specific type 1 response of an immunogenic composition against a viral infection and preserving or increasing a type 2 response of said immunogenic composition comprising:
obtaining a peptide comprising the sequence KLKL 5 KLK (SEQ ID NO: 6) and an I-ODN, wherein the I-ODN comprises oligo-d(IC) 13 (SEQ ID NO: 21); and administering the peptide and the I-ODN with an immunogenic composition against a viral infection to a subject;
wherein the antigen-specific type 1 response to the immunogenic composition against a viral infection is improved in the subject and the type 2 response to the immunogenic composition is preserved or increased in the subject.
27 . The method according to claim 26 wherein the antigen-specific type 1 response is further defined as an IgG2-antibody response or an IFN-gamma response.
28 . The method according to claim 26 wherein the type 2 response is further defined as an IgG1-antibody response or an interleukin-4 (IL-4) response.
29 . The method according to claim 26 wherein the immunogenic composition comprises a viral antigen.
30 . The method according to claim 26 wherein the immunogenic composition further comprises an Al(OH)3 adjuvant.
31 . The method according to claim 29 wherein the viral antigen is derived from HIV, HAV, HBV, HCV, JEV, RSV, EBV, Influenza virus, HPV or Rotavirus.
32 . The method according to claim 26 wherein the immunogenic composition further comprises a polycationic peptide.
33 . The method according to claim 26 wherein the immunogenic composition further comprises an oligodeoxynucleotide containing a CpG-motif.
34 . The method according to claim 26 wherein the immunogenic composition further comprises a polycationic peptide and an oligodeoxynucleotide containing a CpG-motif.Join the waitlist — get patent alerts
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