Methods and nucleic acid molecules for aav vector selection
US-2024417717-A1 · Dec 19, 2024 · US
US9107909B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9107909-B2 |
| Application number | US-200913128074-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 6, 2009 |
| Priority date | Nov 6, 2008 |
| Publication date | Aug 18, 2015 |
| Grant date | Aug 18, 2015 |
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This disclosure is directed to the methods of enhancing hematopoietic stem cells (HSPC) and progenitor cell (HSPC) engraftment procedure. Treatment in vivo of a HSPC donor with compounds that reduce PGE 2 biosynthesis or PGE 2 receptor antagonists alone, or in combination with other hematopoietic mobilization agents such as AMD3100 and G-CSF, increases the circulation of available HSPCs. Compounds that reduce the cellular synthesis of PGE 2 include non-steroidal anti-inflammatory compounds such as indomethacin. Treatment ex vivo of HSPC with an effective amount of PGE 2 or at least one of its derivatives such as 16,16-dimethyl prostaglandin E 2 (dmPGE 2 ), promotes HSPC engraftment. Similar methods may also be used to increase viral-mediated gene transduction efficacy into HSPC.
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What is claimed is: 1. A method of enhancing viral transduction efficacy in a human hematopoietic stem or progenitor cell, comprising the steps of: providing a viral vector that contains at least one gene of interest for transduction; supplying at least one human hematopoietic stem or progenitor cell that has been treated ex vivo with an effective amount of prostaglandin E 2 or a derivative thereof; and transfecting the human hematopoietic stem or progenitor cell treated with…
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