Cultured human mast cells release various chemokines after stimulation with IL-33

Dear Editor, Both acquired and innate immune responses reportedly cause type 2 inflammation, the main pathogenesis underlying such allergic disorders as bronchial asthma. Crosstalk between acquired and innate immune responses involves various cell types and is a critical driver of type 2 inflammatio...

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Veröffentlicht in:Allergology International 2021-07, Vol.70 (3), p.386-388
Hauptverfasser: Maiko Emi-Sugie, Hirohisa Saito, Kenji Matsumoto
Format: Artikel
Sprache:jpn
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Zusammenfassung:Dear Editor, Both acquired and innate immune responses reportedly cause type 2 inflammation, the main pathogenesis underlying such allergic disorders as bronchial asthma. Crosstalk between acquired and innate immune responses involves various cell types and is a critical driver of type 2 inflammation. Among those cells, mast cells play unique roles as a result of being directly activated in both immune responses: acquired immune responses (IgE crosslinking) induce mast cells' degranulation and cytokine and cysteinyl LT production, while innate immune responses (IL-33 and TSLP) induce mast cells' cytokine production. Cytokines are some of the most important mediators in cell-to-cell interactions. In order to work effectively, cytokine-producing cells need to release chemokines that attract their target cells into close proximity. Regarding mast cells, IgE crosslinking reportedly leads to release of several chemokines.
ISSN:1323-8930