Frontiers in Immunology (Feb 2021)

Natural Killer-Like B Cells Secreting Interleukin-18 Induces a Proinflammatory Response in Periodontitis

  • Ye Zhang,
  • Ye Zhang,
  • Ye Zhang,
  • Ye Zhang,
  • Wei Kuang,
  • Danfeng Li,
  • Danfeng Li,
  • Danfeng Li,
  • Yu Li,
  • Yi Feng,
  • Yi Feng,
  • Yi Feng,
  • Xinwei Lyu,
  • Xinwei Lyu,
  • Xinwei Lyu,
  • Gao-Bo Huang,
  • Jian-Qi Lian,
  • Xiao-Fei Yang,
  • Cheng Hu,
  • Cheng Hu,
  • Cheng Hu,
  • Yajuan Xie,
  • Yajuan Xie,
  • Yajuan Xie,
  • Song Xue,
  • Jiali Tan,
  • Jiali Tan,
  • Jiali Tan

DOI
https://doi.org/10.3389/fimmu.2021.641562
Journal volume & issue
Vol. 12

Abstract

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Natural killer-like B (NKB) cells, which are newly identified immune subsets, reveal a critical immunoregulatory property in the eradication of microbial infection via the secretion of interleukin (IL)-18. For the first time, this study investigated the role of NKB cells in secreting IL-18 in the pathogenesis of periodontitis. In this study, NKB cells' percentage and IL-18 concentration in peripheral blood and periodontium in periodontitis patients was measured using flow cytometry and ELISA. The role of IL-18 in regulating periodontal inflammation was examined in a Porphyromonas gingivalis (P. gingivalis)-induced periodontitis murine model. Peripheral and periodontal-infiltrating CD3−CD19+NKp46+ NKB cells, which were the main source of IL-18, were elevated and correlated with attachment loss in periodontitis patients. In vitro IL-18 stimulation promoted proinflammatory cytokine production in periodontal ligament cells. P. gingivalis infection induced elevation of IL-18 receptor in periodontium in a periodontitis murine model. IL-18 neutralization not only suppressed P. gingivalis-induced alveolar bone resorption, but also inhibited recruitment of antigen-non-specific inflammatory cells into the periodontium, probably via dampening expressions of cytokines, chemokines, and matrix metalloproteinases. NKB cells secreting IL-18 appeared to be an important mediator in the inflammatory response following intraoral P. gingivalis infection. These findings might be relevant to the development of immunotherapies for periodontitis.

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