TLR7/8 activation in neutrophils impairs immune complex phagocytosis through shedding of FcgRIIA

Christian Lood, Sabine Arve, Jeffrey Ledbetter, Keith B Elkon

Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskriftPeer review

45 Citeringar (SciVal)

Sammanfattning

Neutrophils play a crucial role in host defense. However, neutrophil activation is also linked to autoimmune diseases such as systemic lupus erythematosus (SLE), where nucleic acid-containing immune complexes (IC) drive inflammation. The role of Toll-like receptor (TLR) signaling in processing of SLE ICs and downstream inflammatory neutrophil effector functions is not known. We observed that TLR7/8 activation leads to a furin-dependent proteolytic cleavage of the N-terminal part of FcgRIIA, shifting neutrophils away from phagocytosis of ICs toward the programmed form of necrosis, NETosis. TLR7/8-activated neutrophils promoted cleavage of FcgRIIA on plasmacytoid dendritic cells and monocytes, resulting in impaired overall clearance of ICs and increased complement C5a generation. Importantly, ex vivo derived activated neutrophils from SLE patients demonstrated a similar cleavage of FcgRIIA that was correlated with markers of disease activity, as well as complement activation. Therapeutic approaches aimed at blocking TLR7/8 activation would be predicted to increase phagocytosis of circulating ICs, while disarming their inflammatory potential.

Originalspråkengelska
Sidor (från-till)2103-2119
Antal sidor17
TidskriftJournal of Experimental Medicine
Volym214
Utgåva7
DOI
StatusPublished - 2017 juni 12
Externt publiceradJa

Bibliografisk information

© 2017 Lood et al.

Ämnesklassifikation (UKÄ)

  • Immunologi inom det medicinska området

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