IL-10 Family Cytokines IL-10 and IL-22: from Basic Science to Clinical Translation

Cytokines are among the most important effector and messenger molecules in the immune system. They profoundly participate in immune responses during infection and inflammation, protecting against or contributing to diseases such as allergy, autoimmunity, and cancer. Manipulating cytokine pathways, t...

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Veröffentlicht in:Immunity (Cambridge, Mass.) Mass.), 2019-04, Vol.50 (4), p.871-891
Hauptverfasser: Ouyang, Wenjun, O’Garra, Anne
Format: Artikel
Sprache:eng
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Zusammenfassung:Cytokines are among the most important effector and messenger molecules in the immune system. They profoundly participate in immune responses during infection and inflammation, protecting against or contributing to diseases such as allergy, autoimmunity, and cancer. Manipulating cytokine pathways, therefore, is one of the most effective strategies to treat various diseases. IL-10 family cytokines exert essential functions to maintain tissue homeostasis during infection and inflammation through restriction of excessive inflammatory responses, upregulation of innate immunity, and promotion of tissue repairing mechanisms. Their important functions in diseases are supported by data from many preclinical models, human genetic studies, and clinical interventions. Despite significant efforts, however, there is still no clinically approved therapy through manipulating IL-10 family cytokines. Here, we summarize the recent progress in understanding the biology of this family of cytokines, suggesting more specific strategies to maneuver these cytokines for the effective treatment of inflammatory diseases and cancers. IL-10 family cytokines play important functions to regulate immune responses and maintain tissue homeostasis during infection, autoimmunity, and cancers. Ouyang and O’Garra review the most recent advance of these cytokines, especially IL-10 and IL-22, and focus on their regulation, biological functions in diseases, and potential translations in clinic.
ISSN:1074-7613
1097-4180
DOI:10.1016/j.immuni.2019.03.020