Methods and nucleic acid molecules for aav vector selection
US-2024417717-A1 · Dec 19, 2024 · US
US10870682B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10870682-B2 |
| Application number | US-201816105346-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 20, 2018 |
| Priority date | Jun 26, 2013 |
| Publication date | Dec 22, 2020 |
| Grant date | Dec 22, 2020 |
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The present invention provides compositions and methods of use comprising a chimeric dengue virus E glycoprotein comprising a dengue virus E glycoprotein backbone, which comprises amino acid substitutions that introduce an epitope that is recognized by an antibody from a dengue virus serotype that is different from the dengue virus serotype of the dengue virus E glycoprotein backbone.
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That which is claimed is: 1. A chimeric dengue virus E glycoprotein comprising a dengue virus E glycoprotein backbone that comprises the following amino acid substitutions that introduce an epitope that is recognized by an antibody that is reactive with a dengue virus serotype that is different from the dengue virus serotype of the dengue virus E glycoprotein backbone; wherein the amino acid residue numbering is based on the reference amino acid sequence of an E glycoprotein of dengue virus serotype 3 (DENV3) identified as SEQ ID NO:1: T138S, Q158H, V160T, S169P, A173I, I174Q, P176T, E177D, N272T, G275T, and S277T, and wherein said dengue virus E glycoprotein further comprises an insertion of the amino acid residues T and E between amino acid residues 155 and 156. 2. A flavivirus particle or virus like particle (VLP) comprising the chimeric dengue virus E glycoprotein of claim 1 . 3. A composition comprising the chimeric dengue virus E glycoprotein of claim 1 in a pharmaceutically acceptable carrier. 4. A composition comprising the flavivirus particle or VLP of claim 2 in a pharmaceutically acceptable carrier. 5. A method of producing an immune response to a dengue virus in a subject, comprising administering to the subject an effective amount of the chimeric dengue virus E glycoprotein of claim 1 . 6. A method of producing an immune response to a dengue virus in a subject, comprising administering to the subject an effective amount of the flavivirus particle or VLP of claim 2 .
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