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A new genetic method to generate and isolate small, short-lived but highly potent dendritic cell-tumor cell hybrid vaccines

A new genetic method to generate and isolate small, short-lived but highly potent dendritic cell-tumor cell hybrid vaccines
A new genetic method to generate and isolate small, short-lived but highly potent dendritic cell-tumor cell hybrid vaccines
Fusion of tumor cells with antigen-presenting cells (APCs) has been proposed for the preparation of cancer vaccines. However, generation of these hybrids, using physical or chemical methods such as electrofusion or polyethylene glycol (PEG), has been difficult to standardize. Characterization of cell fusion has also been problematic because of difficulties in differentiating fusion from cell aggregation, leakage of cellular dyes and dendritic-cell (DC) phagocytosis of tumor material. In this report, we describe a new method to generate hybrid cell vaccines, based on gene transfer of a viral fusogenic membrane glycoprotein (FMG) into tumor cells, and incorporate a genetic method by which true hybrid formation can be unambiguously detected. We describe a new class of tumor cell?DC hybrid that can be rapidly isolated after cell fusion. These hybrids are highly potent in in vitro antigen presentation assays, target lymph nodes in vivo and are powerful immunogens against established metastatic disease.
1078-8956
1215-1219
Phan, Vy
d0420994-e12f-4fad-a454-bee8d9bf9193
Errington, Fiona
a73395e9-c5db-4352-9b74-603142bbedca
Cheong, S. Chiat
bef49dd2-e4fd-4aa9-b929-a85bbab56cbc
Kottke, Tim
76d0e0d3-f397-44bd-9e4b-c8dd2961441f
Gough, Michael
690f0c98-228c-479d-9cec-3415a93467e7
Altmann, Sharon
c1d46b49-f6bb-4026-bc05-3dc181de5f82
Brandenburger, Annick
828fd836-7b00-486d-a60f-2e8a025432c3
Emery, Steve
eb0dff30-3e7f-4dc6-b391-d9ff0e5bfc7b
Strome, Scott
19371cb6-06c9-423c-82bb-cae57c03afa1
Bateman, Andrew
a851558d-8b9b-4020-b148-a239c2b26815
Bonnotte, Bernard
4c48748d-32fa-4ee3-88d1-7e69dfa9259a
Melcher, Alan
68cc1c3e-8ad3-4d82-b1fa-c2a46d05c7ba
Vile, Richard
a2252a95-3f21-447f-ab45-c7fcc888151f
Phan, Vy
d0420994-e12f-4fad-a454-bee8d9bf9193
Errington, Fiona
a73395e9-c5db-4352-9b74-603142bbedca
Cheong, S. Chiat
bef49dd2-e4fd-4aa9-b929-a85bbab56cbc
Kottke, Tim
76d0e0d3-f397-44bd-9e4b-c8dd2961441f
Gough, Michael
690f0c98-228c-479d-9cec-3415a93467e7
Altmann, Sharon
c1d46b49-f6bb-4026-bc05-3dc181de5f82
Brandenburger, Annick
828fd836-7b00-486d-a60f-2e8a025432c3
Emery, Steve
eb0dff30-3e7f-4dc6-b391-d9ff0e5bfc7b
Strome, Scott
19371cb6-06c9-423c-82bb-cae57c03afa1
Bateman, Andrew
a851558d-8b9b-4020-b148-a239c2b26815
Bonnotte, Bernard
4c48748d-32fa-4ee3-88d1-7e69dfa9259a
Melcher, Alan
68cc1c3e-8ad3-4d82-b1fa-c2a46d05c7ba
Vile, Richard
a2252a95-3f21-447f-ab45-c7fcc888151f

Phan, Vy, Errington, Fiona, Cheong, S. Chiat, Kottke, Tim, Gough, Michael, Altmann, Sharon, Brandenburger, Annick, Emery, Steve, Strome, Scott, Bateman, Andrew, Bonnotte, Bernard, Melcher, Alan and Vile, Richard (2003) A new genetic method to generate and isolate small, short-lived but highly potent dendritic cell-tumor cell hybrid vaccines. Nature Medicine, 9 (9), 1215-1219. (doi:10.1038/nm923).

Record type: Article

Abstract

Fusion of tumor cells with antigen-presenting cells (APCs) has been proposed for the preparation of cancer vaccines. However, generation of these hybrids, using physical or chemical methods such as electrofusion or polyethylene glycol (PEG), has been difficult to standardize. Characterization of cell fusion has also been problematic because of difficulties in differentiating fusion from cell aggregation, leakage of cellular dyes and dendritic-cell (DC) phagocytosis of tumor material. In this report, we describe a new method to generate hybrid cell vaccines, based on gene transfer of a viral fusogenic membrane glycoprotein (FMG) into tumor cells, and incorporate a genetic method by which true hybrid formation can be unambiguously detected. We describe a new class of tumor cell?DC hybrid that can be rapidly isolated after cell fusion. These hybrids are highly potent in in vitro antigen presentation assays, target lymph nodes in vivo and are powerful immunogens against established metastatic disease.

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More information

Published date: September 2003
Additional Information: Technical report

Identifiers

Local EPrints ID: 26521
URI: http://eprints.soton.ac.uk/id/eprint/26521
ISSN: 1078-8956
PURE UUID: f9dae9d4-fb6a-4a5e-bdd7-1fb98bb5306e

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Date deposited: 19 Apr 2006
Last modified: 15 Mar 2024 07:11

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Contributors

Author: Vy Phan
Author: Fiona Errington
Author: S. Chiat Cheong
Author: Tim Kottke
Author: Michael Gough
Author: Sharon Altmann
Author: Annick Brandenburger
Author: Steve Emery
Author: Scott Strome
Author: Andrew Bateman
Author: Bernard Bonnotte
Author: Alan Melcher
Author: Richard Vile

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