In situ neutrophil efferocytosis shapes T cell immunity to influenza infection

Early recruitment of neutrophils from the blood to sites of tissue infection is a hallmark of innate immune responses. However, little is known about the mechanisms by which apoptotic neutrophils are cleared in infected tissues during resolution and the immunological consequences of in situ efferocy...

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Veröffentlicht in:Nature immunology 2020-09, Vol.21 (9), p.1046-1057
Hauptverfasser: Lim, Kihong, Kim, Tae-hyoun, Trzeciak, Alissa, Amitrano, Andrea M., Reilly, Emma C., Prizant, Hen, Fowell, Deborah J., Topham, David J., Kim, Minsoo
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Sprache:eng
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Zusammenfassung:Early recruitment of neutrophils from the blood to sites of tissue infection is a hallmark of innate immune responses. However, little is known about the mechanisms by which apoptotic neutrophils are cleared in infected tissues during resolution and the immunological consequences of in situ efferocytosis. Using intravital multiphoton microscopy, we show previously unrecognized motility patterns of interactions between neutrophils and tissue-resident phagocytes within the influenza-infected mouse airway. Newly infiltrated inflammatory monocytes become a chief pool of phagocytes and play a key role in the clearance of highly motile apoptotic neutrophils during the resolution phase. Apoptotic neutrophils further release epidermal growth factor and promote the differentiation of monocytes into tissue-resident antigen-presenting cells for activation of antiviral T cell effector functions. Collectively, these results suggest that the presence of in situ neutrophil resolution at the infected tissue is critical for optimal CD8 + T cell–mediated immune protection. Kim and colleagues provide new insights into the function and fate of neutrophils during influenza infection and their roles in antiviral T cell responses.
ISSN:1529-2908
1529-2916
DOI:10.1038/s41590-020-0746-x