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Early Transcriptional Signature in Dendritic Cells and the Induction of Protective T Cell Responses Upon Immunization With VLPs Containing TLR Ligands—A Role for CCL2

Inducing T cell responses by therapeutic vaccination requires appropriate activation of antigen presenting cells (APCs). The use of virus-like particles (VLPs) containing Toll-like receptor (TLR) ligands has demonstrated remarkable potential in activating APCs and modulating the immune response both...

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Autores principales: Gomes, Ariane C., Mohsen, Mona O., Mueller, Julius E., Leoratti, Fabiana M. S., Cabral-Miranda, Gustavo, Bachmann, Martin F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687836/
https://www.ncbi.nlm.nih.gov/pubmed/31428084
http://dx.doi.org/10.3389/fimmu.2019.01679
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author Gomes, Ariane C.
Mohsen, Mona O.
Mueller, Julius E.
Leoratti, Fabiana M. S.
Cabral-Miranda, Gustavo
Bachmann, Martin F.
author_facet Gomes, Ariane C.
Mohsen, Mona O.
Mueller, Julius E.
Leoratti, Fabiana M. S.
Cabral-Miranda, Gustavo
Bachmann, Martin F.
author_sort Gomes, Ariane C.
collection PubMed
description Inducing T cell responses by therapeutic vaccination requires appropriate activation of antigen presenting cells (APCs). The use of virus-like particles (VLPs) containing Toll-like receptor (TLR) ligands has demonstrated remarkable potential in activating APCs and modulating the immune response both for prophylactic vaccines as well as immunotherapy. Here, we employed VLPs associated to TLR ligands as tools to modulate cytotoxic response mediated by CD8(+) T cells and provide further insight in the development of T cell-based immunotherapy. We have investigated the in vivo transcriptional signature in dendritic cells (DCs) from mice immunized with VLPs containing distinct classes of nucleic acid and correlated the expression patterns with the efficiency of induced T cell responses. We identified key pathways activated in DCs that are involved in the appropriated induction of T cell responses and show evidence for the modulatory effect of CCL2 in CD8(+) T cells responses. These insights shed light on immune networks that are pivotal for the induction of potent cytotoxic T cell responses and identify key genes for appropriate DC activation and subsequent modulation of the adaptive immune response.
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spelling pubmed-66878362019-08-19 Early Transcriptional Signature in Dendritic Cells and the Induction of Protective T Cell Responses Upon Immunization With VLPs Containing TLR Ligands—A Role for CCL2 Gomes, Ariane C. Mohsen, Mona O. Mueller, Julius E. Leoratti, Fabiana M. S. Cabral-Miranda, Gustavo Bachmann, Martin F. Front Immunol Immunology Inducing T cell responses by therapeutic vaccination requires appropriate activation of antigen presenting cells (APCs). The use of virus-like particles (VLPs) containing Toll-like receptor (TLR) ligands has demonstrated remarkable potential in activating APCs and modulating the immune response both for prophylactic vaccines as well as immunotherapy. Here, we employed VLPs associated to TLR ligands as tools to modulate cytotoxic response mediated by CD8(+) T cells and provide further insight in the development of T cell-based immunotherapy. We have investigated the in vivo transcriptional signature in dendritic cells (DCs) from mice immunized with VLPs containing distinct classes of nucleic acid and correlated the expression patterns with the efficiency of induced T cell responses. We identified key pathways activated in DCs that are involved in the appropriated induction of T cell responses and show evidence for the modulatory effect of CCL2 in CD8(+) T cells responses. These insights shed light on immune networks that are pivotal for the induction of potent cytotoxic T cell responses and identify key genes for appropriate DC activation and subsequent modulation of the adaptive immune response. Frontiers Media S.A. 2019-08-02 /pmc/articles/PMC6687836/ /pubmed/31428084 http://dx.doi.org/10.3389/fimmu.2019.01679 Text en Copyright © 2019 Gomes, Mohsen, Mueller, Leoratti, Cabral-Miranda and Bachmann. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Gomes, Ariane C.
Mohsen, Mona O.
Mueller, Julius E.
Leoratti, Fabiana M. S.
Cabral-Miranda, Gustavo
Bachmann, Martin F.
Early Transcriptional Signature in Dendritic Cells and the Induction of Protective T Cell Responses Upon Immunization With VLPs Containing TLR Ligands—A Role for CCL2
title Early Transcriptional Signature in Dendritic Cells and the Induction of Protective T Cell Responses Upon Immunization With VLPs Containing TLR Ligands—A Role for CCL2
title_full Early Transcriptional Signature in Dendritic Cells and the Induction of Protective T Cell Responses Upon Immunization With VLPs Containing TLR Ligands—A Role for CCL2
title_fullStr Early Transcriptional Signature in Dendritic Cells and the Induction of Protective T Cell Responses Upon Immunization With VLPs Containing TLR Ligands—A Role for CCL2
title_full_unstemmed Early Transcriptional Signature in Dendritic Cells and the Induction of Protective T Cell Responses Upon Immunization With VLPs Containing TLR Ligands—A Role for CCL2
title_short Early Transcriptional Signature in Dendritic Cells and the Induction of Protective T Cell Responses Upon Immunization With VLPs Containing TLR Ligands—A Role for CCL2
title_sort early transcriptional signature in dendritic cells and the induction of protective t cell responses upon immunization with vlps containing tlr ligands—a role for ccl2
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687836/
https://www.ncbi.nlm.nih.gov/pubmed/31428084
http://dx.doi.org/10.3389/fimmu.2019.01679
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