Capsid variants and methods of using the same
US-2024417430-A1 · Dec 19, 2024 · US
US9278998B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9278998-B2 |
| Application number | US-82993110-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 2, 2010 |
| Priority date | Jul 2, 2009 |
| Publication date | Mar 8, 2016 |
| Grant date | Mar 8, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention provides HA polypeptides (e.g., H1 HA polypeptides) that bind to umbrella-topology glycans, and reagents and methods relating thereto. The present invention provides binding agents that bind to HA polypeptides (e.g., H1 HA polypeptides), and reagents and methods relating thereto. The present invention provides interfering agents that inhibit the binding of HA polypeptides (e.g., H1 HA polypeptides) to HA receptors, and reagents and methods relating thereto. The present invention provides compositions and methods for treating, preventing, and/or diagnosing influenza infection utilizing HA polypeptides, HA polypeptide binding agents, HA polypeptide interfering agents, and/or vaccine compositions comprising any of the foregoing.
Opening claim text (preview).
We claim: 1. An H1 HA influenza hemagglutinin (“HA”) polypeptide variant whose amino acid sequence: i) shows at least 90% identity with a reference wild type H1 HA polypeptide that is the HA from A/California/04/2009 strain (SEQ ID NO: 46); ii) includes a sequence substitution relative to the reference at each of the following positions: Position Amino (corresponding to acid residue wild type H3 HA) in reference 186 Ser 189 Ala 219 Ile 227 Glu and iii) differs from that of each of ADA76, A/duck/Alberta/35/76 (H1N1) (SEQ ID NO: 23); ASI30, A/Swine/Iowa/30 (H1N1) (SEQ ID NO: 24); APR34, A/Puerto Rico/8/34 (H1N1) (SEQ ID NO: 25); ASC18, A/South Carolina/1/18 (H1N1) (SEQ ID NO: 26); AT91, A/Texas/36/91 (H1N1) (SEQ ID NO: 27); ANY18, A/New York/1/18 (H1N1) (SEQ ID NO: 28); ADU63, A/Duck/Ukraine/1/63 (H3N8) (SEQ ID NO: 29); AAI68, A/Aichi/2/68 (H3N2) (SEQ ID NO: 30); AM99, A/Moscow/10/99 (H3N2) (SEQ ID NO: 31); ADS97, A/Duck/Singapore/3/97 (H5N3) (SEQ ID NO: 32); Viet04, A/Vietnam/1203/2004 (H5N1) (SEQ ID NO: 33). 2. A pharmaceutical composition comprising the H1 HA polypeptide variant of claim 1 . 3. A method of treating influenza infection by administering a composition comprising the H1 HA polypeptide variant of claim 1 to a subject. 4. A vaccine composition comprising the H1 HA polypeptide variant of claim 1 . 5. A method comprising administering the vaccine composition of claim 4 to an individual suffering from or susceptible to influenza virus infection. 6. The H1 HA polypeptide variant of claim 1 , wherein the variant residue at position 219 is Lys. 7. The H1 HA polypeptide variant of claim 1 , wherein the variant residue at position 186 is Pro. 8. The H1 HA polypeptide variant of claim 1 , wherein the variant residue at position 189 is Thr. 9. The H1 HA polypeptide variant of claim 1 , wherein the variant residue at position 227 is Ala. 10. The H1 HA polypeptide variant of claim 1 , whose amino acid sequence further includes one or more sequence substitutions relative to the reference at positions selected from the group consisting of: 98, 136, 137, 138, 145, 153, 155, 156, 159, 183, 187, 190, 192, 193, 194, 195, 196, 215, 222, 225, 226, 228, and combinations thereof, corresponding to positions in wild type H3 HA sequence. 11. The H1 HA polypeptide variant of claim 10 , wherein the variant residue at position 225 is selected from the group consisting of Asn, Gly, and Glu. 12. The H1 HA polypeptide variant of claim 10 , wherein the variant residue at position 145 is selected from the group consisting of Ser and Asn.
Viruses · CPC title
Immunostimulants · CPC title
from viruses · CPC title
New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes · CPC title
for influenza or rhinoviruses · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.