IL-27-induced PD-L1highSca-1+ innate lymphoid cells suppress contact hypersensitivity in an IL-10-dependent manner

Author:

Min Keun Young,Kim Do-KyunORCID,Jo Min Geun,Choi min Yeong,Lee Dajeong,Park Jeong Won,Park Young-Jun,Chung YeonseokORCID,Kim Young Mi,Park Yeong-Min,Kim Hyuk SoonORCID,Choi Wahn Soo

Abstract

AbstractInnate 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 (ILC210s) have an immunoregulatory function dependent on IL-10. However, the surface markers of ILC210s and the role of ILC210s in contact hypersensitivity (CHS) are largely unknown. Our study revealed that splenic ILC210s are extensively included in PD-L1highSca-1+ ILCs and that IL-27 amplifies the development of PD-L1highSca-1+ ILCs and ILC210s. Adoptive transfer of PD-L1highSca-1+ ILCs suppressed oxazolone-induced CHS in an IL-10-dependent manner Taken together, our results demonstrate that ILC210s are critical for the control of CHS and suggest that ILC210s can be used as target cells for the treatment of CHS.

Funder

National Research Foundation of Korea

Publisher

Springer Science and Business Media LLC

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