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Induction of Antiviral Cytotoxic T Cells by Plasmacytoid Dendritic Cells for Adoptive Immunotherapy of Posttransplant Diseases

Authors :
Henri Vié
Joel Plumas
Marie-Jeanne Richard
Caroline Aspord
David Laurin
Laurence Chaperot
Institute for Advanced Biosciences / Institut pour l'Avancée des Biosciences (Grenoble) (IAB)
Centre Hospitalier Universitaire [Grenoble] (CHU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Etablissement français du sang - Auvergne-Rhône-Alpes (EFS)-Université Grenoble Alpes [2016-2019] (UGA [2016-2019])
Etablissement français du sang - Auvergne-Rhône-Alpes (EFS)
Recherches en cancérologie
Université de Nantes (UN)-IFR26-Institut National de la Santé et de la Recherche Médicale (INSERM)
Source :
American Journal of Transplantation, American Journal of Transplantation, Wiley, 2011, 11 (12), pp.2613-2626. ⟨10.1111/j.1600-6143.2011.03722.x⟩
Publication Year :
2011
Publisher :
HAL CCSD, 2011.

Abstract

Virus-associated hematologic malignancies (EBV lymphoproliferative disease) and opportunistic infections (CMV) represent a major cause of hematopoietic stem cell and solid organ transplantation failure. Adoptive transfer of antigen-specific T lymphocytes appears to be a major and successful immunotherapeutic strategy, but improvements are needed to reliably produce high numbers of virus-specific T cells with appropriate requirements for adoptive immunotherapy that would allow extensive clinical use. Since plasmacytoid dendritic cells (pDCs) are crucial in launching antiviral responses, we investigated their capacity to elicit functional antiviral T-cell responses for adoptive cellular immunotherapy using a unique pDC line and antigens derived from Influenza, CMV and EBV viruses. Stimulation of peripheral blood mononuclear cells from HLA-A*0201(+) donors by HLA-A0201 matched pDCs pulsed with viral-derived peptides triggered high levels of multi-specific and functional cytotoxic T-cell responses (up to 99% tetramer(+) CD8 T cells) in vitro. Furthermore, the central/effector memory cytotoxic T cells elicited by the pDCs strongly display antiviral activity upon adoptive transfer into a humanized mouse model that mimics a virus-induced malignancy. We provide a simple and potent method to generate virus-specific CTL with the required properties for adoptive cellular immunotherapy of post-transplant diseases.

Details

Language :
English
ISSN :
16006135 and 16006143
Database :
OpenAIRE
Journal :
American Journal of Transplantation, American Journal of Transplantation, Wiley, 2011, 11 (12), pp.2613-2626. ⟨10.1111/j.1600-6143.2011.03722.x⟩
Accession number :
edsair.doi.dedup.....adf742ce6f6bbbdaf9985956c250e3cf
Full Text :
https://doi.org/10.1111/j.1600-6143.2011.03722.x⟩