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

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作者
Keun Young Min
Do-Kyun Kim
Min Geun Jo
min Yeong Choi
Dajeong Lee
Jeong Won Park
Young-Jun Park
Yeonseok Chung
Young Mi Kim
Yeong-Min Park
Hyuk Soon Kim
Wahn Soo Choi
机构
[1] Konkuk University,Department of Immunology, School of Medicine
[2] Jeonbuk National University,Korea Zoonosis Research Institute
[3] The Graduate School of Dong-A University,Department of Biomedical Sciences, College of Natural Science and Department of Health Sciences
[4] Jeju National University,College of Pharmacy
[5] Seoul National University,Research Institute of Pharmaceutical Sciences, College of Pharmacy
[6] Duksung Women’s University,Department of Preventive Pharmacy, College of Pharmacy
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摘要
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 (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.
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页码:616 / 629
页数:13
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