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IL10- and IL35-Secreting MutuDC Lines Act in Cooperation to Inhibit Memory T Cell Activation Through LAG-3 Expression

Dendritic cells (DCs) are professional antigen-presenting cells involved in the initiation of immune responses. We generated a tolerogenic DC (tolDC) line that constitutively secretes interleukin-10 (IL10-DCs), expressed lower levels of co-stimulatory and MHCII molecules upon stimulation, and induce...

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Autores principales: Koga, Marianna M., Engel, Adrien, Pigni, Matteo, Lavanchy, Christine, Stevanin, Mathias, Laversenne, Vanessa, Schneider, Bernard L., Acha-Orbea, Hans
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925845/
https://www.ncbi.nlm.nih.gov/pubmed/33679743
http://dx.doi.org/10.3389/fimmu.2021.607315
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author Koga, Marianna M.
Engel, Adrien
Pigni, Matteo
Lavanchy, Christine
Stevanin, Mathias
Laversenne, Vanessa
Schneider, Bernard L.
Acha-Orbea, Hans
author_facet Koga, Marianna M.
Engel, Adrien
Pigni, Matteo
Lavanchy, Christine
Stevanin, Mathias
Laversenne, Vanessa
Schneider, Bernard L.
Acha-Orbea, Hans
author_sort Koga, Marianna M.
collection PubMed
description Dendritic cells (DCs) are professional antigen-presenting cells involved in the initiation of immune responses. We generated a tolerogenic DC (tolDC) line that constitutively secretes interleukin-10 (IL10-DCs), expressed lower levels of co-stimulatory and MHCII molecules upon stimulation, and induced antigen-specific proliferation of T cells. Vaccination with IL10-DCs combined with another tolDC line that secretes IL-35, reduced antigen-specific local inflammation in a delayed-type hypersensitivity assay independently on regulatory T cell differentiation. In an autoimmune model of rheumatoid arthritis, vaccination with the combined tolDCs after the onset of the disease impaired disease development and promoted recovery of mice. After stable memory was established, the tolDCs promoted CD4 downregulation and induced lymphocyte activation gene 3 (LAG-3) expression in reactivated memory T cells, reducing T cell activation. Taken together, our findings indicate the benefits of combining anti-inflammatory cytokines in an antigen-specific context to treat excessive inflammation when memory is already established.
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spelling pubmed-79258452021-03-04 IL10- and IL35-Secreting MutuDC Lines Act in Cooperation to Inhibit Memory T Cell Activation Through LAG-3 Expression Koga, Marianna M. Engel, Adrien Pigni, Matteo Lavanchy, Christine Stevanin, Mathias Laversenne, Vanessa Schneider, Bernard L. Acha-Orbea, Hans Front Immunol Immunology Dendritic cells (DCs) are professional antigen-presenting cells involved in the initiation of immune responses. We generated a tolerogenic DC (tolDC) line that constitutively secretes interleukin-10 (IL10-DCs), expressed lower levels of co-stimulatory and MHCII molecules upon stimulation, and induced antigen-specific proliferation of T cells. Vaccination with IL10-DCs combined with another tolDC line that secretes IL-35, reduced antigen-specific local inflammation in a delayed-type hypersensitivity assay independently on regulatory T cell differentiation. In an autoimmune model of rheumatoid arthritis, vaccination with the combined tolDCs after the onset of the disease impaired disease development and promoted recovery of mice. After stable memory was established, the tolDCs promoted CD4 downregulation and induced lymphocyte activation gene 3 (LAG-3) expression in reactivated memory T cells, reducing T cell activation. Taken together, our findings indicate the benefits of combining anti-inflammatory cytokines in an antigen-specific context to treat excessive inflammation when memory is already established. Frontiers Media S.A. 2021-02-17 /pmc/articles/PMC7925845/ /pubmed/33679743 http://dx.doi.org/10.3389/fimmu.2021.607315 Text en Copyright © 2021 Koga, Engel, Pigni, Lavanchy, Stevanin, Laversenne, Schneider and Acha-Orbea. 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
Koga, Marianna M.
Engel, Adrien
Pigni, Matteo
Lavanchy, Christine
Stevanin, Mathias
Laversenne, Vanessa
Schneider, Bernard L.
Acha-Orbea, Hans
IL10- and IL35-Secreting MutuDC Lines Act in Cooperation to Inhibit Memory T Cell Activation Through LAG-3 Expression
title IL10- and IL35-Secreting MutuDC Lines Act in Cooperation to Inhibit Memory T Cell Activation Through LAG-3 Expression
title_full IL10- and IL35-Secreting MutuDC Lines Act in Cooperation to Inhibit Memory T Cell Activation Through LAG-3 Expression
title_fullStr IL10- and IL35-Secreting MutuDC Lines Act in Cooperation to Inhibit Memory T Cell Activation Through LAG-3 Expression
title_full_unstemmed IL10- and IL35-Secreting MutuDC Lines Act in Cooperation to Inhibit Memory T Cell Activation Through LAG-3 Expression
title_short IL10- and IL35-Secreting MutuDC Lines Act in Cooperation to Inhibit Memory T Cell Activation Through LAG-3 Expression
title_sort il10- and il35-secreting mutudc lines act in cooperation to inhibit memory t cell activation through lag-3 expression
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925845/
https://www.ncbi.nlm.nih.gov/pubmed/33679743
http://dx.doi.org/10.3389/fimmu.2021.607315
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