Gene sequence construct for gene therapy of human immunodeficiency virus infection
US-2024352096-A1 · Oct 24, 2024 · US
US9534041B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9534041-B2 |
| Application number | US-201414767274-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 11, 2014 |
| Priority date | Feb 12, 2013 |
| Publication date | Jan 3, 2017 |
| Grant date | Jan 3, 2017 |
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Monoclonal neutralizing antibodies are disclosed that specifically bind to a Norovirus. In some embodiments, the Norovirus is a genogroup II Norovirus or a Genogroup II Norovirus. In some embodiments, the Norovirus is Norwalk virus. In some embodiments, the monoclonal antibodies specifically bind VP1. Also disclosed are compositions including the disclosed antibodies, nucleic acids encoding these antibodies, expression vectors including the nucleic acids, and isolated host cells that express the nucleic acids. The antibodies and compositions disclosed herein can be used for detecting the presence of a Norovirus in a biological sample, or detecting a Norovirus infection. In addition, the neutralization ability of the disclosed antibodies makes them ideal for treating a subject with a Norovirus infection. Thus, disclosed are methods of treating and/or preventing these infections.
Opening claim text (preview).
We claim: 1. An isolated monoclonal antibody comprising a heavy chain variable domain and a light chain variable domain, wherein the heavy chain variable domain comprises a heavy chain complementarity determining region (HCDR)1, an HCDR2 and an HCDR3, wherein the light chain variable domain comprises an LCDR1, and LCDR2 and an LCDR3, and wherein (a) the HCDR1 comprises the amino acid sequence set forth as SEQ ID NO: 18, the HCDR2 comprises the amino acid sequence set forth as SEQ ID NO: 20, and the HCDR3 comprises the amino acid sequence set forth as SEQ ID NO: 22 and the LCDR1 comprises the amino acid sequence set forth as SEQ ID NO: 26, the LCDR2 comprises the amino acid sequence set forth as SEQ ID NO: 28, and the LCDR3 comprises the amino acid sequence set forth as SEQ ID NO: 30; (b) the HCDR1 comprises the amino acid sequence set forth as SEQ ID NO: 2, the HCDR2 comprises the amino acid sequence set forth as SEQ ID NO: 4, and the HCDR3 comprises the amino acid sequence set forth as SEQ ID NO: 6 and the LCDR1 comprises the amino acid sequence set forth as SEQ ID NO: 10, the LCDR2 comprises the amino acid sequence set forth as SEQ ID NO: 12, and the LCDR3 comprises the amino acid sequence set forth as SEQ ID NO: 14; (c) the HCDR1 comprises the amino acid sequence set forth as SEQ ID NO: 34, the HCDR2 comprises the amino acid sequence set forth as SEQ ID NO: 36, and the HCDR3 comprises the amino acid sequence set forth as SEQ ID NO: 38 and the LCDR1 comprises the amino acid sequence set forth as SEQ ID NO: 42, the LCDR2 comprises the amino acid sequence set forth as SEQ ID NO: 44, and the LCDR3 comprises the amino acid sequence set forth as SEQ ID NO: 46; (d) the HCDR1 comprises the amino acid sequence set forth as SEQ ID NO: 50, the HCDR2 comprises the amino acid sequence set forth as SEQ ID NO: 52, and the HCDR3 comprises the amino acid sequence set forth as SEQ ID NO: 54 and the LCDR1 comprises the amino acid sequence set forth as SEQ ID NO: 58, the LCDR2 comprises the amino acid sequence set forth as SEQ ID NO: 60, and the LCDR3 comprises the amino acid sequence set forth as SEQ ID NO: 62; or (e) the HCDR1 comprises the amino acid sequence set forth in SEQ ID NO: 66, the HCDR2 comprises the amino acid sequence set forth in SEQ ID NO: 68, and the HCDR3 comprises the amino acid sequence set forth as SEQ ID NO: 70 and the LCDR1 comprises the amino acid sequence set forth as SEQ ID NO: 74, the LCDR2 comprises the amino acid sequence set forth as SEQ ID NO: 76, and the LCDR3 comprises the amino acid sequence set forth as SEQ ID NO: 78, and wherein the monoclonal antibody specifically binds to a Norwalk Virus viral protein (VP)1 with a K D of 1 nM or less. 2. The isolated monoclonal antibody of claim 1 , wherein the heavy chain variable domain comprises the amino acid sequence set forth as one of SEQ ID NO: 8, SEQ ID NO: 24, SEQ ID NO: 40, SEQ ID NO: 56, or SEQ ID NO: 72. 3. The isolated monoclonal antibody of claim 1 , wherein the light chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 16, SEQ ID NO: 32, SEQ ID NO: 48, SEQ ID NO: 64, or SEQ ID NO: 80. 4. The isolated monoclonal antibody of claim 1 , wherein: (a) the heavy chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 8 and the light chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 16; (b) the heavy chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 24 and the light chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 32; (c) the heavy chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 40 and the light chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 48; (d) the heavy chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 56 and the light chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 64; or (e) the heavy chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 72 and the light chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 80. 5. The isolated monoclonal antibody of claim 1 , wherein the antibody is an IgG, IgM or IgA. 6. The isolated monoclonal antibody of claim 1 , wherein the antibody is humanized or chimeric. 7. An isolated antigen binding fragment of the isolated monoclonal antibody of claim 1 . 8. The isolated antigen binding fragment of claim 7 , wherein the fragment is a Fab fragment, a Fab′ fragment, a F(ab)′ 2 fragment, a single chain Fv protein (scFv), or a disulfide stabilized Fv protein (dsFv). 9. The isolated antigen binding fragment of claim 8 , wherein the antigen binding fragment is a Fab or an scFv fragment. 10. The isolated monoclonal antibody of claim 1 , or an antigen binding fragment thereof, wherein the antibody or the antigen binding fragment is labeled. 11. The isolated monoclonal antibody or antigen binding fragment of claim 10 , wherein the label is a fluorescent, an enzymatic, or a radioactive label. 12. A composition comprising an effective amount of the antibody of claim 1 , or an antigen binding fragment thereof, and a pharmaceutically acceptable carrier. 13. An isolated nucleic acid molecule encoding the monoclonal antibody of claim 1 , or an antigen binding fragment thereof. 14. The isolated nucleic acid molecule of claim 13 , operably linked to a promoter. 15. An expression vector comprising the isolated nucleic acid molecule of claim 14 . 16. An isolated host cell transformed with the expression vector of claim 15 . 17. A method of detecting a Norwalk virus infection in a subject comprising: contacting a biological sample from the subject with at least one isolated monoclonal antibody of claim 1 or an antigen binding fragment thereof; and detecting antibody bound to the sample, wherein the presence of antibody bound to the sample indicates that the subject has an Norwalk virus infection. 18. The method of claim 17 , wherein the isolated monoclonal antibody is directly labeled. 19. The method of claim 17 , further comprising: contacting the sample with a second antibody that specifically binds the isolated human monoclonal antibody; and detecting the binding of the second antibody, wherein an increase in binding of the second antibody to the sample as compared to binding of the second antibody to a control sample detects the presence of an Norovirus infection the subject. 20. A method for treating a Norwalk virus infection in a subject, comprising administering to the subject a therapeutically effective amount of at least one antibody of claim 1 , an antigen binding fragment thereof, or a nucleic acid encoding the antibody or the antibody fragment thereby treating the Norwalk virus. 21. The method of 20 , further comprising administering to the subject an anti-viral agent. 22. The method of claim 17 , further comprising measuring viral titer in the subject. 23. A composition comprising an effective amount of the nucleic acid molecule of claim 13 or an expression vector comprising the nucleic acid molecule operably linked to a promoter; and a pharmaceutically acceptable carrier. 24. The isolated monoclonal antibody of claim 1 , wherein the HCDR1 comprises the amino acid sequence set forth as SEQ ID NO: 18, the HCDR2 comprises the amino acid sequence set forth as SEQ ID NO: 20, and the HCDR3 comprises the amino acid
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