US2012164177A1PendingUtilityA1
Rhinovirus vaccines
Est. expiryJan 19, 2025(expired)· nominal 20-yr term from priority
A61P 31/16A61P 37/04C12N 2770/32722C07K 14/005C12N 2770/32734A61K 39/00
41
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Claims
Abstract
The present invention relates generally to peptide vaccines. More specifically, the present invention relates to vaccines against rhinoviruses and other related and non-related pathogenic animal viruses. In addition, the present invention relates generally to methods of designing and producing vaccines against viruses and, in certain embodiments, against rhinoviruses and other pathogenic viruses.
Claims
exact text as granted — not AI-modified1 - 32 . (canceled)
33 - 42 . (canceled)
43 . A method of producing a vaccine against a picornavirus, which comprises:
(a) identifying transiently exposed regions of capsid proteins within at least a majority of serotypes comprising a target picornavirus; (b) obtaining amino acid sequence information for at least a majority of said transiently exposed regions of capsid proteins; (c) identifying amino acid sequences within said transiently exposed regions exhibiting a preferred level of sequence conservation; and (d) producing a peptide vaccine that is functionally equivalent to at least a majority of the amino acid sequences within said transiently exposed regions exhibiting a preferred level of sequence conservation.
44 . The method of claim 43 , which further comprises immunizing at least one host animal with the peptide vaccine and collecting antisera from said host animal.
45 . The method of claim 44 , which further comprises testing said antisera for pan-serotypic activity.
46 . The method of claim 45 , wherein said testing is carried out using a viral neutralization assay.
47 . The method of claim 43 , wherein the transiently exposed regions of capsid proteins are identified across at least 70% of the serotypes that comprise the target picornavirus.
48 . The method of claim 43 , wherein the transiently exposed regions of capsid proteins are identified across at least 90% of the serotypes that comprise the target picornavirus.
49 . The method of claim 43 , wherein the peptide vaccine is conjugated to or associated with a carrier molecule.
50 . The method of claim 43 , wherein the peptide vaccine is added to an adjuvant.
51 . A method of producing a vaccine against rhinoviruses, which comprises:
(a) identifying transiently exposed regions of VP4 capsid proteins within at least a majority of rhinovirus serotypes; (b) obtaining amino acid sequence information for at least a majority of said transiently exposed regions of VP4 capsid proteins; (c) identifying amino acid sequences within said transiently exposed regions exhibiting a preferred level of sequence conservation; and (d) producing one or more peptide vaccines, wherein the one or more peptide vaccines are collectively functionally equivalent to at least a majority of the amino acid sequences within said transiently exposed regions exhibiting a preferred level of sequence conservation.
52 . The method of claim 51 , which further comprises immunizing at least one host animal with one or more peptide vaccines and collecting antisera from such host animal.
53 . The method of claim 52 , which further comprises testing said antisera for rhinovirus pan-serotypic activity.
54 . The method of claim 53 , wherein said testing is carried out using a viral neutralization assay.
55 . The method of claim 54 , wherein the transiently exposed regions of VP4 capsid proteins are identified across at least 70% of rhinovirus serotypes.
56 . The method of claim 54 , wherein the transiently exposed regions of VP4 capsid proteins are identified across at least 90% of rhinovirus serotypes.
57 . The method of claim 51 , wherein the one or more peptide vaccines are conjugated to, or associated with, a carrier molecule.
58 . The method of claim 51 , wherein the one or more peptide vaccines are added to an adjuvant.
59 . The method of claim 51 , wherein the transiently exposed regions of VP4 capsid proteins are located near the N-termini thereof.
60 . A method for immunizing a mammal against rhinovirus infection, which comprises providing to a mammal an effective amount of one or more peptide vaccines, wherein the one or more peptide vaccines are functionally equivalent to transiently exposed regions of rhinovirus VP4 capsid proteins.
61 . The method of claim 60 , wherein the transiently exposed regions of rhinovirus VP4 capsid proteins are located near the N-termini thereof.Cited by (0)
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