IL-27-induced PD-L1 high Sca-1 + innate lymphoid cells suppress contact hypersensitivity in an IL-10-dependent manner.
Keun Young MinDo-Kyun KimMin Geun JoMin Yeong ChoiDajeong LeeJeong Won ParkYoung-Jun ParkYeonseok ChungYoung Mi KimYeong-Min ParkHyuk Soon KimWahn Soo ChoiPublished in: Experimental & molecular medicine (2024)
Innate lymphoid cells (ILCs) play an important role in maintaining tissue homeostasis and various inflammatory responses. ILCs are typically classified into three subsets, as is the case for T-cells. Recent studies have reported that IL-10-producing type 2 ILCs (ILC2 10 s) have an immunoregulatory function dependent on IL-10. However, the surface markers of ILC2 10 s and the role of ILC2 10 s in contact hypersensitivity (CHS) are largely unknown. Our study revealed that splenic ILC2 10 s are extensively included in PD-L1 high Sca-1 + ILCs and that IL-27 amplifies the development of PD-L1 high Sca-1 + ILCs and ILC2 10 s. Adoptive transfer of PD-L1 high Sca-1 + ILCs suppressed oxazolone-induced CHS in an IL-10-dependent manner Taken together, our results demonstrate that ILC2 10 s are critical for the control of CHS and suggest that ILC2 10 s can be used as target cells for the treatment of CHS.