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Prostaglandin E(2) in a TLR3- and 7/8-agonist-based DC maturation cocktail generates mature, cytokine-producing, migratory DCs but impairs antigen cross-presentation to CD8(+) T cells

Mature dendritic cells (DCs) represent cellular adjuvants for optimal antigen presentation in cancer vaccines. Recently, a combination of prostaglandin E(2) (PGE(2)) with Toll-like receptor agonists (TLR-P) was proposed as a new standard to generate superior cytokine-producing DCs with high migrator...

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Autores principales: Gierlich, Philipp, Lex, Veronika, Technau, Antje, Keupp, Anne, Morper, Lorenz, Glunz, Amelie, Sennholz, Hanno, Rachor, Johannes, Sauer, Sascha, Marcu, Ana, Grigoleit, Götz Ulrich, Wölfl, Matthias, Schlegel, Paul G., Eyrich, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7223547/
https://www.ncbi.nlm.nih.gov/pubmed/32100075
http://dx.doi.org/10.1007/s00262-019-02470-1
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author Gierlich, Philipp
Lex, Veronika
Technau, Antje
Keupp, Anne
Morper, Lorenz
Glunz, Amelie
Sennholz, Hanno
Rachor, Johannes
Sauer, Sascha
Marcu, Ana
Grigoleit, Götz Ulrich
Wölfl, Matthias
Schlegel, Paul G.
Eyrich, Matthias
author_facet Gierlich, Philipp
Lex, Veronika
Technau, Antje
Keupp, Anne
Morper, Lorenz
Glunz, Amelie
Sennholz, Hanno
Rachor, Johannes
Sauer, Sascha
Marcu, Ana
Grigoleit, Götz Ulrich
Wölfl, Matthias
Schlegel, Paul G.
Eyrich, Matthias
author_sort Gierlich, Philipp
collection PubMed
description Mature dendritic cells (DCs) represent cellular adjuvants for optimal antigen presentation in cancer vaccines. Recently, a combination of prostaglandin E(2) (PGE(2)) with Toll-like receptor agonists (TLR-P) was proposed as a new standard to generate superior cytokine-producing DCs with high migratory capacity. Here, we compare TLR-P DCs with conventional DCs matured only with the proinflammatory cytokines TNFα and IL-1ß (CDCs), focussing on the interaction of resulting DCs with CD8(+) T-cells. TLR-P matured DCs showed elevated expression of activation markers such as CD80 and CD83 compared to CDCs, together with a significantly higher migration capacity. Secretion of IL-6, IL-8, IL-10, and IL-12 was highest after 16 h in TLR-P DCs, and only TLR-P DCs secreted active IL-12p70. TLR-P DCs as well as CDCs successfully primed multifunctional CD8(+) T-cells from naïve precursors specific for the peptide antigens Melan-A, NLGN4X, and PTP with comparable priming efficacy and T-cell receptor avidity. CD8(+) T-cells primed by TLR-P DCs showed significantly elevated expression of the integrin VLA-4 and a trend for higher T-cell numbers after expansion. In contrast, TLR-P DCs displayed a substantially reduced capability to cross-present CMVpp65 protein antigen to pp65-specific T cells, an effect that was dose-dependent on PGE(2) during DC maturation and reproducible with several responder T-cell lines. In conclusion, TLR-P matured DCs might be optimal presenters of antigens not requiring processing such as short peptides. However, PGE(2) seems less favorable for maturation of DCs intended to process and cross-present more complex vaccine antigens such as lysates, proteins or long peptides. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00262-019-02470-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-72235472020-05-15 Prostaglandin E(2) in a TLR3- and 7/8-agonist-based DC maturation cocktail generates mature, cytokine-producing, migratory DCs but impairs antigen cross-presentation to CD8(+) T cells Gierlich, Philipp Lex, Veronika Technau, Antje Keupp, Anne Morper, Lorenz Glunz, Amelie Sennholz, Hanno Rachor, Johannes Sauer, Sascha Marcu, Ana Grigoleit, Götz Ulrich Wölfl, Matthias Schlegel, Paul G. Eyrich, Matthias Cancer Immunol Immunother Original Article Mature dendritic cells (DCs) represent cellular adjuvants for optimal antigen presentation in cancer vaccines. Recently, a combination of prostaglandin E(2) (PGE(2)) with Toll-like receptor agonists (TLR-P) was proposed as a new standard to generate superior cytokine-producing DCs with high migratory capacity. Here, we compare TLR-P DCs with conventional DCs matured only with the proinflammatory cytokines TNFα and IL-1ß (CDCs), focussing on the interaction of resulting DCs with CD8(+) T-cells. TLR-P matured DCs showed elevated expression of activation markers such as CD80 and CD83 compared to CDCs, together with a significantly higher migration capacity. Secretion of IL-6, IL-8, IL-10, and IL-12 was highest after 16 h in TLR-P DCs, and only TLR-P DCs secreted active IL-12p70. TLR-P DCs as well as CDCs successfully primed multifunctional CD8(+) T-cells from naïve precursors specific for the peptide antigens Melan-A, NLGN4X, and PTP with comparable priming efficacy and T-cell receptor avidity. CD8(+) T-cells primed by TLR-P DCs showed significantly elevated expression of the integrin VLA-4 and a trend for higher T-cell numbers after expansion. In contrast, TLR-P DCs displayed a substantially reduced capability to cross-present CMVpp65 protein antigen to pp65-specific T cells, an effect that was dose-dependent on PGE(2) during DC maturation and reproducible with several responder T-cell lines. In conclusion, TLR-P matured DCs might be optimal presenters of antigens not requiring processing such as short peptides. However, PGE(2) seems less favorable for maturation of DCs intended to process and cross-present more complex vaccine antigens such as lysates, proteins or long peptides. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00262-019-02470-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-02-25 2020 /pmc/articles/PMC7223547/ /pubmed/32100075 http://dx.doi.org/10.1007/s00262-019-02470-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Gierlich, Philipp
Lex, Veronika
Technau, Antje
Keupp, Anne
Morper, Lorenz
Glunz, Amelie
Sennholz, Hanno
Rachor, Johannes
Sauer, Sascha
Marcu, Ana
Grigoleit, Götz Ulrich
Wölfl, Matthias
Schlegel, Paul G.
Eyrich, Matthias
Prostaglandin E(2) in a TLR3- and 7/8-agonist-based DC maturation cocktail generates mature, cytokine-producing, migratory DCs but impairs antigen cross-presentation to CD8(+) T cells
title Prostaglandin E(2) in a TLR3- and 7/8-agonist-based DC maturation cocktail generates mature, cytokine-producing, migratory DCs but impairs antigen cross-presentation to CD8(+) T cells
title_full Prostaglandin E(2) in a TLR3- and 7/8-agonist-based DC maturation cocktail generates mature, cytokine-producing, migratory DCs but impairs antigen cross-presentation to CD8(+) T cells
title_fullStr Prostaglandin E(2) in a TLR3- and 7/8-agonist-based DC maturation cocktail generates mature, cytokine-producing, migratory DCs but impairs antigen cross-presentation to CD8(+) T cells
title_full_unstemmed Prostaglandin E(2) in a TLR3- and 7/8-agonist-based DC maturation cocktail generates mature, cytokine-producing, migratory DCs but impairs antigen cross-presentation to CD8(+) T cells
title_short Prostaglandin E(2) in a TLR3- and 7/8-agonist-based DC maturation cocktail generates mature, cytokine-producing, migratory DCs but impairs antigen cross-presentation to CD8(+) T cells
title_sort prostaglandin e(2) in a tlr3- and 7/8-agonist-based dc maturation cocktail generates mature, cytokine-producing, migratory dcs but impairs antigen cross-presentation to cd8(+) t cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7223547/
https://www.ncbi.nlm.nih.gov/pubmed/32100075
http://dx.doi.org/10.1007/s00262-019-02470-1
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