mRNA: From a chemical blueprint for protein production to an off-the-shelf therapeutic

Two decades ago, mRNA became the focus of research in molecular medicine and was proposed as an active pharmaceutical ingredient for the therapy of cancer. In this regard, mRNA has been mainly used for ex vivo modification of antigen-presenting cells (APCs), such as dendritic cells (DCs). This vacci...

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Main Authors: Van Lint, Sandra, Heirman, Carlo, Thielemans, Kris, Breckpot, Karine
Format: Online
Language:English
Published: Landes Bioscience 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859745/
id pubmed-3859745
recordtype oai_dc
spelling pubmed-38597452013-12-16 mRNA: From a chemical blueprint for protein production to an off-the-shelf therapeutic Van Lint, Sandra Heirman, Carlo Thielemans, Kris Breckpot, Karine Commentary Two decades ago, mRNA became the focus of research in molecular medicine and was proposed as an active pharmaceutical ingredient for the therapy of cancer. In this regard, mRNA has been mainly used for ex vivo modification of antigen-presenting cells (APCs), such as dendritic cells (DCs). This vaccination strategy has proven to be safe, well tolerated and capable of inducing tumor antigen-specific immune responses. Recently, the direct application of mRNA for in situ modification of APCs, hence immunization was shown to be feasible and at least as effective as DC-based immunization in pre-clinical models. It is believed that application of mRNA as an off-the-shelf vaccine represents an important step in the development of future cancer immunotherapeutic strategies. Here, we will discuss the use of ex vivo mRNA-modified DCs and “naked mRNA” for cancer immunotherapy focusing on parameters such as the employed DC subtype, DC activation stimulus and route of immunization. In addition, we will provide an overview on the clinical trials published so far, trying to link their outcome to the aforementioned parameters. Landes Bioscience 2013-02-01 2013-01-04 /pmc/articles/PMC3859745/ /pubmed/23291946 http://dx.doi.org/10.4161/hv.22661 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Van Lint, Sandra
Heirman, Carlo
Thielemans, Kris
Breckpot, Karine
spellingShingle Van Lint, Sandra
Heirman, Carlo
Thielemans, Kris
Breckpot, Karine
mRNA: From a chemical blueprint for protein production to an off-the-shelf therapeutic
author_facet Van Lint, Sandra
Heirman, Carlo
Thielemans, Kris
Breckpot, Karine
author_sort Van Lint, Sandra
title mRNA: From a chemical blueprint for protein production to an off-the-shelf therapeutic
title_short mRNA: From a chemical blueprint for protein production to an off-the-shelf therapeutic
title_full mRNA: From a chemical blueprint for protein production to an off-the-shelf therapeutic
title_fullStr mRNA: From a chemical blueprint for protein production to an off-the-shelf therapeutic
title_full_unstemmed mRNA: From a chemical blueprint for protein production to an off-the-shelf therapeutic
title_sort mrna: from a chemical blueprint for protein production to an off-the-shelf therapeutic
description Two decades ago, mRNA became the focus of research in molecular medicine and was proposed as an active pharmaceutical ingredient for the therapy of cancer. In this regard, mRNA has been mainly used for ex vivo modification of antigen-presenting cells (APCs), such as dendritic cells (DCs). This vaccination strategy has proven to be safe, well tolerated and capable of inducing tumor antigen-specific immune responses. Recently, the direct application of mRNA for in situ modification of APCs, hence immunization was shown to be feasible and at least as effective as DC-based immunization in pre-clinical models. It is believed that application of mRNA as an off-the-shelf vaccine represents an important step in the development of future cancer immunotherapeutic strategies. Here, we will discuss the use of ex vivo mRNA-modified DCs and “naked mRNA” for cancer immunotherapy focusing on parameters such as the employed DC subtype, DC activation stimulus and route of immunization. In addition, we will provide an overview on the clinical trials published so far, trying to link their outcome to the aforementioned parameters.
publisher Landes Bioscience
publishDate 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859745/
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