Innate lymphoid cells and allergic inflammation
Highlights•Group 2 innate lymphoid cells (ILC2s) have been implicated in the pathogenesis
of multiple allergic diseases including asthma, chronic rhinosinusitis and atopic
dermatitis.•In addition to IL-25, IL-33, and TSLP, ILC2s are regulated by eicosanoids.•Recent
studies indicate that ILC2s influence both innate and adaptive immune cell function.Group 2
innate lymphoid cells (ILC2s) play critical roles in anti-helminth immunity and airway
epithelial repair. Recently, these cells have also emerged as key players in the development …
of multiple allergic diseases including asthma, chronic rhinosinusitis and atopic
dermatitis.•In addition to IL-25, IL-33, and TSLP, ILC2s are regulated by eicosanoids.•Recent
studies indicate that ILC2s influence both innate and adaptive immune cell function.Group 2
innate lymphoid cells (ILC2s) play critical roles in anti-helminth immunity and airway
epithelial repair. Recently, these cells have also emerged as key players in the development …
Highlights
- Group 2 innate lymphoid cells (ILC2s) have been implicated in the pathogenesis of multiple allergic diseases including asthma, chronic rhinosinusitis and atopic dermatitis.
- In addition to IL-25, IL-33, and TSLP, ILC2s are regulated by eicosanoids.
- Recent studies indicate that ILC2s influence both innate and adaptive immune cell function.
Group 2 innate lymphoid cells (ILC2s) play critical roles in anti-helminth immunity and airway epithelial repair. Recently, these cells have also emerged as key players in the development of allergic inflammation at multiple barrier surfaces. ILC2s arise from common lymphoid progenitors in the bone marrow, are dependent on the transcription factors RORα, GATA3, and TCF-1 and produce the type 2 cytokines IL-4, IL-5, IL-9, and/or IL-13. The epithelial cell-derived cytokines IL-25, IL-33, and TSLP regulate the activation and effector functions of ILC2s, and recent studies suggest that their responsiveness to these cytokines and other factors may depend on their tissue environment. In this review, we focus on recent advances in our understanding of how ILC2s are differentially regulated in the context of allergic inflammation and discuss the therapeutic potential of targeting ILC2s in the treatment of allergic diseases.
Elsevier