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Type I interferon is required for T helper (Th) 2 induction by dendritic cells

Type 2 inflammation is a defining feature of infection with parasitic worms (helminths), as well as being responsible for widespread suffering in allergies. However, the precise mechanisms involved in T helper (Th) 2 polarization by dendritic cells (DCs) are currently unclear. We have identified a p...

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Detalles Bibliográficos
Autores principales: Webb, Lauren M, Lundie, Rachel J, Borger, Jessica G, Brown, Sheila L, Connor, Lisa M, Cartwright, Adam NR, Dougall, Annette M, Wilbers, Ruud HP, Cook, Peter C, Jackson‐Jones, Lucy H, Phythian‐Adams, Alexander T, Johansson, Cecilia, Davis, Daniel M, Dewals, Benjamin G, Ronchese, Franca, MacDonald, Andrew S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556270/
https://www.ncbi.nlm.nih.gov/pubmed/28716804
http://dx.doi.org/10.15252/embj.201695345
Descripción
Sumario:Type 2 inflammation is a defining feature of infection with parasitic worms (helminths), as well as being responsible for widespread suffering in allergies. However, the precise mechanisms involved in T helper (Th) 2 polarization by dendritic cells (DCs) are currently unclear. We have identified a previously unrecognized role for type I IFN (IFN‐I) in enabling this process. An IFN‐I signature was evident in DCs responding to the helminth Schistosoma mansoni or the allergen house dust mite (HDM). Further, IFN‐I signaling was required for optimal DC phenotypic activation in response to helminth antigen (Ag), and efficient migration to, and localization with, T cells in the draining lymph node (dLN). Importantly, DCs generated from Ifnar1 (−/−) mice were incapable of initiating Th2 responses in vivo. These data demonstrate for the first time that the influence of IFN‐I is not limited to antiviral or bacterial settings but also has a central role to play in DC initiation of Th2 responses.