Type III interferon primes pDCs for TLR7 activation and antagonizes immune suppression mediated by TGF-β and PGE2

Conventional dendritic cell and plasmacytoid dendritic cell (pDC) subsets have specialized functions that can be modulated by the tumor microenvironment, and produce different interferons that are central to antitumor immune responses. While the function of type I interferons in tumor immunity is well characterized, that of type III interferons produced by type 1 conventional dendritic cells in the tumor microenvironment remains unclear. Here we demonstrate in vitro that type III interferons orchestrate pDC survival, activation and TLR7 expression in the blood, thereby enhancing pDC responses to a TLR7 ligand. Moreover, we show that tumor-associated pDCs express the highest level of IFNLR1, and that these immune cell subsets are the most responsive to IFN-III. Importantly, type III interferons prevent the inhibition of pDCs induced by TGF-β or PGE2 in tumor soluble milieu from patients to restores production of IFN-α in pDCs. With TGF-β or PGE2 having pleotropic functions in immune regulation, our results thus implicate IFN-III-mediated immune modulation to have broad impact on various pathological situations.

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Publication Details

Journal
Nature Communications
Published
2025-03-28
DOI
https://doi.org/10.1038/s41467-025-58220-8
Citations
13
Primary Topic
Immune Response and Inflammation
Type
article
Field-Weighted Citation Impact
9.57

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article

Type III interferon primes pDCs for TLR7 activation and antagonizes immune suppression mediated by TGF-β and PGE2

Léo Laoubi, Candice Sakref, Maude Ardin, Anne‐Claire Doffin et al.
13 citations
Nature Communications
Immune Response and Inflammation
9.57
article

Type III interferon primes pDCs for TLR7 activation and antagonizes immune suppression mediated by TGF-β and PGE2

Léo Laoubi, Candice Sakref, Maude Ardin, Anne‐Claire Doffin, Jan P. Böttcher, Margaux Hubert, Nathalie Bendriss‐Vermare, Lyvia Moudombi, Aurélien Voissière, Stéphane Depil, Céline Rodriguez, Élisa Gobbini, Jenny Valladeau‐Guilemond, Christophe Caux, Alexis Saby, Laurie Besson
article en
13 citations

Abstract

Conventional dendritic cell and plasmacytoid dendritic cell (pDC) subsets have specialized functions that can be modulated by the tumor microenvironment, and produce different interferons that are central to antitumor immune responses. While the function of type I interferons in tumor immunity is well characterized, that of type III interferons produced by type 1 conventional dendritic cells in the tumor microenvironment remains unclear. Here we demonstrate in vitro that type III interferons orchestrate pDC survival, activation and TLR7 expression in the blood, thereby enhancing pDC responses to a TLR7 ligand. Moreover, we show that tumor-associated pDCs express the highest level of IFNLR1, and that these immune cell subsets are the most responsive to IFN-III. Importantly, type III interferons prevent the inhibition of pDCs induced by TGF-β or PGE2 in tumor soluble milieu from patients to restores production of IFN-α in pDCs. With TGF-β or PGE2 having pleotropic functions in immune regulation, our results thus implicate IFN-III-mediated immune modulation to have broad impact on various pathological situations.

Nature CommunicationsVol. 16(1)
Université Claude Bernard Lyon 1 (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), Centre de Recherche en Neurosciences de Lyon (FR), Centre Léon Bérard (FR), Centre de Recherche en Cancérologie de Lyon (FR), Technical University of Munich (DE), University of Tübingen (DE)
Ligue Contre le Cancer, Institut National Du Cancer, European Society for Medical Oncology
Openalex Percentile: Top 2%
Immune Response and Inflammation
9.57
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