Journal
MUCOSAL IMMUNOLOGY
Volume 10, Issue 4, Pages 1056-1068Publisher
SPRINGERNATURE
DOI: 10.1038/mi.2016.113
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Funding
- INSERM
- CNRS
- VIB, Ghent University [BOF 01N02313, BOF01J11113, BOF14/GOA/013]
- Fund for Scientific Research-Flanders [G030212N, G011315N]
- European Research Council [281600]
- AZM foundation
- French Institute of cancer (INCa)
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Traditionally regarded as simple foot soldiers of the innate immune response limited to the eradication of pathogens, neutrophils recently emerged as more complex cells endowed with a set of immunoregulatory functions. Using a model of invasive pneumococcal disease, we highlighted an unexpected key role for neutrophils as accessory cells in innate interleukin (IL)-17A production by lung resident V gamma 6V delta 1 (+) Tcells via nucleotide-binding oligomerization domain receptor, pyrin-containing 3 (NLRP3) inflammasome-dependent IL-1 beta secretion. In vivo activation of the NLRP3 inflammasome in neutrophils required both host-derived and bacterial-derived signals. Elaborately, it relies on (i) alveolar macrophage-secreted TNF-alpha for priming and (ii) subsequent exposure to bacterial pneumolysin for activation. Interestingly, this mechanism can be translated to human neutrophils. Our work revealed the cellular and molecular dynamic events leading to gamma delta T17 cell activation, and highlighted for the first time the existence of a fully functional NLRP3 inflammasome in lung neutrophils. This immune axis thus regulates the development of a protective host response to respiratory bacterial infections.
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