CD1dhiPD-L1hiCD27+ Regulatory Natural Killer Subset Suppresses Atopic Dermatitis

Effector and regulatory functions of various leukocytes in allergic diseases have been well reported. Although the role of conventional natural killer (NK) cells has been established, information on its regulatory phenotype and function are very limited. Therefore, the objective of this study was to...

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Published inFrontiers in immunology Vol. 12; p. 752888
Main Authors Min, Keun Young, Koo, Jimo, Noh, Geunwoong, Lee, Dajeong, Jo, Min Geun, Lee, Ji Eon, Kang, Minseong, Hyun, Seung Yeun, Choi, Wahn Soo, Kim, Hyuk Soon
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 05.01.2022
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Summary:Effector and regulatory functions of various leukocytes in allergic diseases have been well reported. Although the role of conventional natural killer (NK) cells has been established, information on its regulatory phenotype and function are very limited. Therefore, the objective of this study was to investigate the phenotype and inhibitory functions of transforming growth factor (TGF)-β-producing regulatory NK (NKreg) subset in mice with MC903-induced atopic dermatitis (AD). Interestingly, the population of TGF-β-producing NK cells in peripheral blood monocytes (PBMCs) was decreased in AD patients than in healthy subjects. The number of TGF-β + NK subsets was decreased in the spleen or cervical lymph node (cLN), but increased in ear tissues of mice with AD induced by MC903 than those of normal mice. We further observed that TGF-β + NK subsets were largely included in CD1d hi PD-L1 hi CD27 + NK cell subset. We also found that numbers of ILC2s and T H 2 cells were significantly decreased by adoptive transfer of CD1d hi PD-L1 hi CD27 + NK subsets. Notably, the ratio of splenic Treg per T H 2 was increased by the adoptive transfer of CD1d hi PD-L1 hi CD27 + NK cells in mice. Taken together, our findings demonstrate that the TGF-β-producing CD1d hi PD-L1 hi CD27 + NK subset has a previously unrecognized role in suppressing T H 2 immunity and ILC2 activation in AD mice, suggesting that the function of TGF-β-producing NK subset is closely associated with the severity of AD in humans.
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Reviewed by: Chang Ook Park, Yonsei University College of Medicine, South Korea; Aimee Beaulieu, The State University of New Jersey, United States
These authors have contributed equally to this work
This article was submitted to NK and Innate Lymphoid Cell Biology, a section of the journal Frontiers in Immunology
Edited by: Teresa Bellon, University Hospital La Paz Research Institute (IdiPAZ), Spain
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2021.752888