Trypanosoma cruzi trans-sialidase initiates a program independent of the transcription factors RORgt and Ahr that leads to IL-17 production by activated B cells

BERMEJO, DANIELA A; JACKSON, SHAUN; GOROSITO SERRAN, MELISA; ACOSTA RODRIGUEZ E V; AMEZCUA VESELY, MARIA CAROLINA; SATHER, B; SINGH, AK; KHIM, S; MUCCI, JUAN; LIGGITT, D; CAMPETELLA, O; OUKKA, MOHAMED; GRUPPI, A; RAWLINGS, DAVID J

NATURE PUBLISHING GROUP

Año: 2013 p. 514 - 514

RUPPI AND RAWLINGS CONTRIBUTED EQUALLY TO THIS WORKHere we identified B cells as a major source of rapid, innate-like production of interleukin 17 (IL-17) in vivo in response to infection with Trypanosoma cruzi. IL-17(+) B cells had a plasmablast phenotype, outnumbered cells of the TH17 subset of helper T cells and were required for an optimal response to this pathogen. With both mouse and human primary B cells, we found that exposure to parasite-derived trans-sialidase in vitro was sufficient to trigger modification of the cell-surface mucin CD45, which led to signaling dependent on the kinase Btk and production of IL-17A or IL-17F via a transcriptional program independent of the transcription factors RORγt and Ahr. Our combined data suggest that the generation of IL-17(+) B cells may be a previously unappreciated feature of innate immune responses required for pathogen control or IL-17-mediated autoimmunity.