Studies on the most efficient vector systems for gene transduction into dendritic cells.

Abstract:

:Specialized antigen-presenting cells (APC), known as dendritic cells (DC), play a pivotal role in initiating primary immune responses. Several vector systems, including adenoviral vectors, retroviral vectors, hemagglutinating virus of Japan-related vectors, and the electroporation, have been shown to transduce genes into mouse and human but not rat DC. However, there is no direct evidence to support the view that the currently used vector systems are able to transduce genes into mature DC. Inasmuch as most, if not all, gene transfer studies investigating DC or DC-related cell populations are performed employing heterogeneous-groups of cells, it is therefore important to determine the extent to which gene transduction occurs in bona fide DC. In this study, we provide evidence that none of these vector systems are able to transfer genes into mature rat DC, which are derived from bone marrow cells (BMC), driven by Flt3/Flk2 ligand and IL-6, and purified with CD161a. Nevertheless, the most efficient gene transduction was observed with developing DC progenitor cells during long-term culture of rat BMC. Successful gene transfer was achieved after 2-week culture with an HIV-based lentiviral vector system.

journal_name

Transplant Proc

authors

Satoh E,Yan H,Miyagi T,Li XK,Sugiura W,Yamamoto N,Teramoto K,Arii S,Kimura H

doi

10.1016/j.transproceed.2004.12.234

subject

Has Abstract

pub_date

2005-01-01 00:00:00

pages

12-4

issue

1

eissn

0041-1345

issn

1873-2623

pii

S0041-1345(04)01692-6

journal_volume

37

pub_type

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