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IgA Triggers Cell Death of Neutrophils When Primed by Inflammatory Mediators
Author(s) -
Marc Wehrli,
Christoph Schneider,
Fabiola Cortinas-Elizondo,
Daniëlle Verschoor,
Kayluz Frias Boligan,
Olivia Adams,
Ruslan Hlushchuk,
Christine Engelmann,
Fritz Daudel,
Peter M. Villiger,
Frank Seibold,
Nikhil Yawalkar,
Cédric Vonarburg,
Sylvia Miescher,
Marius Lötscher,
Thomas Kaufmann,
Christian Münz,
Christoph Mueller,
Valentin Djonov,
HansUwe Simon,
Stephan von Gunten
Publication year - 2020
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1900883
Subject(s) - immunology , medicine , sepsis , rheumatoid arthritis , programmed cell death , inflammation , immune system , apoptosis , biology , biochemistry
IVIG preparations consisting of pooled IgG are increasingly used for the treatment of autoimmune diseases. IVIG is known to regulate the viability of immune cells, including neutrophils. We report that plasma-derived IgA efficiently triggers death of neutrophils primed by cytokines or TLR agonists. IgA-mediated programmed neutrophil death was PI3K-, p38 MAPK-, and JNK-dependent and evoked anti-inflammatory cytokines in macrophage cocultures. Neutrophils from patients with acute Crohn's disease, rheumatoid arthritis, or sepsis were susceptible to both IgA- and IVIG-mediated death. In contrast to IVIG, IgA did not promote cell death of quiescent neutrophils. Our findings suggest that plasma-derived IgA might provide a therapeutic option for the treatment of neutrophil-associated inflammatory disorders.

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