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  3. IgA Triggers Cell Death of Neutrophils When Primed by Inflammatory Mediators.
 

IgA Triggers Cell Death of Neutrophils When Primed by Inflammatory Mediators.

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BORIS DOI
10.7892/boris.147625
Date of Publication
November 15, 2020
Publication Type
Article
Division/Institute

Institut für Pharmako...

Institut für Patholog...

Institut für Anatomie...

Universitätsklinik fü...

Universitätsklinik fü...

Author
Wehrli, Marc
Schneider, Christoph
Cortinas-Elizondo, Fabiola
Verschoor, Daniëlle
Institut für Pharmakologie
Frias Boligan, Kayluz
Institut für Pharmakologie
Adams, Olivia Joan
Institut für Pharmakologie
Hlushchuk, Ruslan
Institut für Anatomie, Topographische und Klinische Anatomie
Institut für Anatomie
Engelmann, Christine
Daudel, Fritz
Villiger, Peter
Universitätsklinik für Rheumatologie, Immunologie und Allergologie
Seibold, Frank
Yawalkar, Nikhil
Universitätsklinik für Dermatologie
Vonarburg, Cédric
Miescher, Sylvia
Lötscher, Marius
Kaufmann, Thomasorcid-logo
Institut für Pharmakologie
Münz, Christian
Müller, Christophorcid-logo
Institut für Pathologie
Institut für Pathologie, Immunpathologie
Djonov, Valentin Georgievorcid-logo
Institut für Anatomie, Topographische und Klinische Anatomie
Institut für Anatomie
Simon, Hans-Uweorcid-logo
Institut für Pharmakologie
von Gunten, Stephan
Institut für Pharmakologie
Subject(s)

600 - Technology::610...

500 - Science::570 - ...

Series
Journal of immunology
ISSN or ISBN (if monograph)
0022-1767
Publisher
American Association of Immunologists
Language
English
Publisher DOI
10.4049/jimmunol.1900883
PubMed ID
33008951
Description
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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/45077
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File(s)
FileFile TypeFormatSizeLicensePublisher/Copright statementContent
jimmunol.1900883.full.pdfAdobe PDF2.13 MBpublished
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