Interleukin-31 monoclonal antibody
US-10421807-B2 · Sep 24, 2019 · US
US12534517B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12534517-B2 |
| Application number | US-201816765509-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 21, 2018 |
| Priority date | Nov 21, 2017 |
| Publication date | Jan 27, 2026 |
| Grant date | Jan 27, 2026 |
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Provided herein, in some embodiments, are compositions of Zika-specific antibodies and antigen-binding fragments thereof and methods of using the antibodies and antigen-binding fragments.
Opening claim text (preview).
We claim: 1 . A method of treating a subject with Zika virus, comprising administering an effective amount of a composition to the subject, wherein the composition comprises: (a) an antibody or an antigen-binding antibody fragment that binds Domain I of Zika virus (ZIKV) Envelope protein (EDI), binds ZIKV strain MR766, or binds ZIKV Envelope protein III (EDIII), wherein the antibody or antigen-binding antibody fragment comprises a heavy chain variable region and a light chain variable region, and wherein: (i) the heavy chain variable region comprises an amino acid sequence that is identical to SEQ ID NO: 1 and the light chain variable region comprises an amino acid sequence that is identical to SEQ ID NO: 2; or (ii) the heavy chain variable region comprises an amino acid sequence that is identical to SEQ ID NO: 3 and the light chain variable region comprises an amino acid sequence that is identical to SEQ ID NO: 4; and (b) a pharmaceutically acceptable carrier. 2 . The method of claim 1 , wherein the antigen-binding antibody fragment is an scFv. 3 . The method of claim 1 , wherein the antibody is a full-length antibody. 4 . The method of claim 3 , wherein the full-length antibody is an IgG molecule. 5 . The method of claim 1 , wherein the antibody or the antigen-binding antibody fragment does not neutralize Dengue viruses 1-4. 6 . The method of claim 1 , wherein the antibody or the antigen-binding antibody fragment is encoded by a nucleic acid. 7 . The method of claim 1 , wherein the antibody is a human antibody. 8 . The method of claim 1 , wherein the composition is administered intramuscularly, subcutaneously, or intravenously. 9 . The method of claim 1 , wherein the subject is a human subject.
Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein · CPC title
Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value · CPC title
Antagonist effect on antigen, e.g. neutralization or inhibition of binding · CPC title
Single chain antibody (scFv) · CPC title
Complementarity determining region [CDR] · CPC title
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