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

  • 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*
  • *Corresponding author for this work
  • Konkuk University
  • Dong-A University
  • Jeju National University
  • Seoul National University
  • Duksung Women's University

Research output: Contribution to journalJournal articlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)616-629
Number of pages14
JournalExperimental and Molecular Medicine
Volume56
Issue number3
DOIs
StatePublished - 2024.03

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Biological Sciences

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