Migration of murine intestinal dendritic cell subsets upon intrinsic and extrinsic TLR3 stimulation

Agnès Garcias López, Vasileios Bekiaris, Katarzyna Müller Luda, Julia Hütter, Isabel Ulmert, Konjit Getachew Muleta, Joy Nakawesi, Knut Kotarsky, Bernard Malissen, Meredith O'Keeffe, Bernhard Holzmann, William Agace, Katharina Lahl

Research output: Contribution to journalArticlepeer-review

7 Citations (SciVal)

Abstract

Initiation of adaptive immunity to particulate antigens in lymph nodes largely depends on their presentation by migratory dendritic cells (DCs). DC subsets differ in their capacity to induce specific types of immunity, allowing subset-specific DC-targeting to influence vaccination and therapy outcomes. Faithful drug design, however, requires exact understanding of subset-specific versus global activation mechanisms. cDC1, the subset of DCs that excel in supporting immunity towards viruses, intracellular bacteria and tumors, express uniquely high levels of the pattern recognition receptor TLR3. Using various murine genetic models, we show here that both, the cDC1 and cDC2 subsets of cDCs are activated and migrate equally well in response to TLR3 stimulation in a cell extrinsic and TNFα dependent manner, but that cDC1 show a unique requirement for type I interferon signaling. Our findings reveal common and differing pathways regulating DC subset migration, offering important insights for the design of DC-based vaccination and therapy approaches. This article is protected by copyright. All rights reserved.

Original languageEnglish
Pages (from-to)1525-1536
Number of pages12
JournalEuropean Journal of Immunology
Volume50
Issue number10
Early online date2020 May 8
DOIs
Publication statusPublished - 2020 Oct

Bibliographical note

This article is protected by copyright. All rights reserved.

Subject classification (UKÄ)

  • Immunology in the medical area

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