IgA Triggers Cell Death of Neutrophils When Primed by Inflammatory Mediators.
Marc WehrliChristoph SchneiderFabiola Cortinas-ElizondoDaniëlle VerschoorKayluz Frias BoliganOlivia Joan AdamsRuslan HlushchukChristine EngelmannFritz DaudelPeter M VilligerFrank SeiboldNikhil YawalkarCédric VonarburgSylvia MiescherMarius LötscherThomas KaufmannChristian MünzChristoph MuellerValentin DjonovHans-Uwe SimonStephan von GuntenPublished in: Journal of immunology (Baltimore, Md. : 1950) (2020)
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.
Keyphrases
- cell death
- rheumatoid arthritis
- oxidative stress
- adipose tissue
- cell cycle arrest
- clinical trial
- intensive care unit
- acute kidney injury
- inflammatory response
- magnetic resonance imaging
- computed tomography
- cell proliferation
- combination therapy
- interstitial lung disease
- study protocol
- septic shock
- endoplasmic reticulum stress