US2021206812A1PendingUtilityA1
Identification and Attenuation of the Immunosuppressive Domains in Fusion Proteins of Enveloped RNA Viruses
Est. expiryOct 7, 2031(~5.2 yrs left)· nominal 20-yr term from priority
A61K 39/12C12N 2770/24234C12N 2770/24122C12N 2760/16234C07K 14/08C12N 2770/24222C12N 2770/24322C12N 2760/16322C07K 4/02C12N 2760/12221C12N 7/00C12N 2770/24321C07K 14/005C12N 2760/16134C12N 2760/16121C12N 2760/12122C12N 2770/24134C12N 2770/36221C07K 1/00C12N 2760/16221C12N 2760/16321C12N 2770/24121C12N 2770/24221C12N 2760/12222C12N 2760/16122C12N 2770/28034C07K 7/08C12N 2770/36121C12N 2770/36222C12N 2770/36122C12N 2770/28021C12N 2760/16222C12N 2760/12121
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Claims
Abstract
The present invention relates to enveloped RNA viruses. The invention in particular relates to the generation of superior antigens for mounting an immune response by first identifying then mutating the immunosuppressive domains in fusion proteins of enveloped RNA viruses resulting in decreased immunosuppressive properties of viral envelope proteins from the viruses.
Claims
exact text as granted — not AI-modified1 . A synthetic peptide comprising the amino acid sequence of SEQ ID NO:4, optionally harboring 1 or 2 or 3 or 4 or 5 or 6 or 7 or 8 or 9 or 10 or 11 point mutation(s), and further comprising a cysteine residue at an N-terminal or C-terminal position.
2 . The synthetic peptide according to claim 1 , wherein the amino acid sequence of SEQ ID NO:4 harbors 1 or 2 or 3 point mutation(s).
3 . The synthetic peptide according to claim 1 , wherein said point mutation(s) are selected from the group consisting of at least one exchange of an amino acid with another amino acid, at least one insertion, at least one deletion, or a combination of one or more of these.
4 . The synthetic peptide according to claim 1 , wherein said synthetic peptide comprises the amino acid sequence of SEQ ID NO:214, optionally harboring 1 or 2 or 3 or 4 or 5 or 6 or 7 or 8 or 9 or 10 or 11 point mutation(s).
5 . The synthetic peptide according to claim 4 , wherein the amino acid sequence of SEQ ID NO:214 harbors 1 or 2 or 3 point mutation(s).
6 . The synthetic peptide according to claim 1 , wherein said synthetic peptide is a dimeric form of said synthetic peptide and wherein said synthetic peptide is dimerized through said cysteine residue.
7 . The synthetic peptide according to claim 6 , wherein said dimerization is through a disulfide bond involving said cysteine residue.
8 . The synthetic peptide according to claim 4 , wherein said synthetic peptide is a dimeric form of said synthetic peptide and wherein said synthetic peptide is dimerized through said cysteine residue.
9 . The synthetic peptide according to claim 8 , wherein said dimerization is through a disulfide bond involving said cysteine residue.
10 . A nucleic acid sequence encoding the synthetic peptide according to claim 1 .
11 . A method of treating or ameliorating the symptoms of an individual, or prophylactic treating an individual, comprising administering an amount of the synthetic peptide according to claim 1 .
12 . A pharmaceutical composition comprising the synthetic peptide according to claim 1 .
13 . The pharmaceutical composition according to claim 12 , further comprising at least one pharmaceutically acceptable excipient, diluent or carrier.
14 . A synthetic peptide comprising an amino acid sequence with at least 75% sequence identity to SEQ ID NO:4, and further comprising a cysteine residue at an N-terminal or C-terminal position.
15 . The synthetic peptide according to claim 14 , wherein said synthetic peptide comprises an amino acid sequence with at least 75% sequence identity to SEQ ID NO:214.
16 . The synthetic peptide according to claim 14 , wherein said synthetic peptide is a dimeric form of said synthetic peptide and wherein said synthetic peptide is dimerized through said cysteine residue.
17 . The synthetic peptide according to claim 16 , wherein said dimerization is through a disulfide bond involving said cysteine residue.
18 . The synthetic peptide according to claim 15 , wherein said synthetic peptide is a dimeric form of said synthetic peptide and wherein said synthetic peptide is dimerized through said cysteine residue.
19 . The synthetic peptide according to claim 18 , wherein said dimerization is through a disulfide bond involving said cysteine residue.
20 . A method of treating or ameliorating the symptoms of an individual, or prophylactic treating an individual, comprising administering an amount of the synthetic peptide according to claim 14 .Join the waitlist — get patent alerts
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