Kelly Wemyss, Lauren M Webb, Hayley M Bridgeman, Ian E Prise, Rufus H Daw, Verena Kästele, Tovah N Shaw, Sabrina Tamburrano, Seona Thompson, Elia D Tait Wojno, Pedro H Papotto, Richard K Grencis, Andrew S MacDonald, Jennifer S Cavet, Joanne E Konkel, Kathryn J Else, John R Grainger
Alterations to monocyte output and function occur during infections driving T helper 1 (TH1)-type inflammation. The degree to which monocytes respond to infections initiating alternative types of responses is poorly understood. Here, we describe a distinct state of the monocyte compartment associated with type 2-polarizing intestinal helminths. Unexpectedly, the adapted monocyte state in a type 2 setting was associated with acquisition of an interferon (IFN) signature. This IFN-induced state provided helminth-infected animals with systemic protection against secondary bacterial infection and allowed for the development of effective type 2 immunity. This pathway of monocyte education was distinct from that in TH1 settings and involved an endogenous bacteria-mediated induction of type I IFN that led to adaptive lymphocyte-dependent IFN-γ priming of monocytes. These findings reveal an IFN-driven mechanism of monocyte education that enables the host to be simultaneously protected against type 2 infections at barrier sites and type 1 infections in the circulation.