US2019275137A1PendingUtilityA1
Immunogenic Influenza Composition
Est. expiryFeb 21, 2028(~1.6 yrs left)· nominal 20-yr term from priority
A61K 2039/53A61K 2039/55566A61K 2039/58A61P 31/16C07K 14/005C12N 7/00A61K 39/12A61K 39/145C12N 2760/16122C12N 2760/16034C12N 2760/16134C12N 2760/16123
60
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Claims
Abstract
Novel compositions useful as influenza immunogens are provided. The compositions enable a host response to immunogen sites normally not recognized by a host.
Claims
exact text as granted — not AI-modified1 - 10 . (canceled)
11 . A method of generating an immune response reactive with more than two serotypes of influenza virus comprising administering to a host an isolated composition comprising a dampened immunodominant epitope and an immunogenic subdominant epitope, wherein said antibody binds said subdominant epitope on said more than two serotypes of influenza virus.
12 . The method of claim 11 , wherein said immunodominant epitope comprises a hemagglutinin.
13 . The method of claim 11 , wherein said immunodominant epitope comprises a neuraminidase.
14 . The method of claim 11 , wherein said immunodominant epitope comprises addition or removal of a glycosylation site.
15 . The method of claim 11 , wherein said immunodominant epitope comprises an amino acid addition, an amino acid substitution or an amino acid deletion.
16 . The method of claim 11 , wherein said immunodominant epitope comprises more than one mutation.
17 . The method of claim 11 , wherein said immunodominant epitope comprises a change to an amino acid.
18 . The method of claim 11 , wherein said composition comprises an influenza virus particle.
19 . The method of claim 11 , wherein said composition comprises a virus-like particle.
20 . The method of claim 11 , wherein said composition is expressed on the surface of an influenza virus.
21 . The method of claim 11 , wherein said composition comprises an immunogenic composition.
22 . The method of claim 11 , wherein said composition further comprises a pharmaceutically acceptable carrier, excipient or diluent.
23 . The method of claim 11 , wherein said composition comprises a nucleic acid encoding said immunodominant epitope.
24 . The method of claim 11 , wherein said composition comprises a polypeptide comprising said immunodominant epitope.
25 . The method of claim 11 , wherein said composition comprises a recombinant virus.
26 . The method of claim 11 , wherein said host comprises an animal.
27 . The method of claim 11 , wherein said influenza virus comprises an influenza A.
28 . The method of claim 11 , wherein said administering occurs before said host comprises an influenza disease.
29 . The method of claim 11 , wherein said immune response comprises antibody.
30 . The method of claim 29 , further comprising isolating said antibody.Join the waitlist — get patent alerts
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