Compositions and methods relating to universal glycoforms for enhanced antibody efficacy
US-2015344544-A1 · Dec 3, 2015 · US
US9321829B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9321829-B2 |
| Application number | US-201214350632-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 18, 2012 |
| Priority date | Oct 18, 2011 |
| Publication date | Apr 26, 2016 |
| Grant date | Apr 26, 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.
Antibodies that specifically bind influenza virus hemagglutinin A (HA), and antigen binding fragments thereof are disclosed herein. In several embodiments, these antibodies are broadly neutralizing. Nucleic acids encoding these monoclonal antibodies, vectors including these nucleic acids, and host cells transformed with these vectors are also disclosed. Compositions are disclosed that include these antibodies, antigen binding fragments, nucleic acids, vectors and host cells. Method of using these antibodies, and antigen binding fragments, nucleic acids, vectors and host cells, such as for diagnosis and treatment of an influenza virus infection are also provided.
Opening claim text (preview).
We claim: 1. A non-naturally occurring chimeric monoclonal antibody, wherein the monoclonal antibody comprises a heavy chain variable domain and a light chain variable domain, wherein the heavy chain variable domain comprising the amino acid sequence set forth as SEQ ID NO: 3, the amino acid sequence set forth as SEQ ID NO: 5, and the amino acid sequence set forth as SEQ ID NO: 7 and the light chain variable domain comprising the amino acid sequence set forth as SEQ ID NO: 13, the amino acid sequence set forth as SEQ ID NO: 15, and the amino acid sequence set forth as SEQ ID NO: 17, and wherein the monoclonal antibody specifically binds hemagglutinin (HA) of at least two of H1N1 and H5N1. 2. The non-naturally occurring chimeric monoclonal antibody of claim 1 , wherein the monoclonal antibody specifically binds HA of H3N2. 3. The non-naturally occurring chimeric monoclonal antibody of claim 1 , wherein the heavy chain variable domain comprises an amino acid sequence set forth as SEQ ID NO: 9. 4. The non-naturally occurring chimeric monoclonal antibody of claim 1 , wherein the light chain variable domain comprises an amino acid sequence set forth as SEQ ID NO: 19. 5. The non-naturally occurring chimeric monoclonal antibody of claim 1 , wherein the antibody is an IgG, IgM or IgA. 6. The non-naturally occurring chimeric monoclonal antibody of claim 1 , wherein the antibody is labeled. 7. The non-naturally occurring chimeric monoclonal antibody of claim 6 , wherein the label is a fluorescent, enzymatic, or radioactive label. 8. A composition comprising the non-naturally occurring chimeric antibody of claim 1 and a pharmaceutically acceptable carrier. 9. A purified nucleic acid molecule encoding the non-naturally occurring chimeric monoclonal antibody of claim 1 . 10. The purified nucleic acid molecule of claim 9 , comprising a nucleotide sequence set forth as SEQ ID NO: 8. 11. An expression vector comprising a nucleic acid comprising SEQ ID NO: 8.
Viruses · CPC title
F(ab')2 · CPC title
Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity · CPC title
Antagonist effect on antigen, e.g. neutralization or inhibition of binding · CPC title
from primates, e.g. man · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.