論文

国際誌
2022年9月

Circadian rhythm affects the magnitude of contact hypersensitivity response in mice.

Allergy
  • Toshiya Miyake
  • Gyohei Egawa
  • Zachary Chow
  • Ryota Asahina
  • Masayuki Otsuka
  • Saeko Nakajima
  • Takashi Nomura
  • Rintaro Shibuya
  • Yoshihiro Ishida
  • Satoshi Nakamizo
  • Teruasa Murata
  • Akihiko Kitoh
  • Kenji Kabashima
  • 全て表示

77
9
開始ページ
2748
終了ページ
2759
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1111/all.15314

BACKGROUND: The circadian rhythm controls multiple biological processes, including immune responses; however, its impact on cutaneous adaptive immune response remains unclear. METHODS: We used a well-established cutaneous type IV allergy model, contact hypersensitivity (CHS). We induced CHS using dinitrofluorobenzene (DNFB). Mice were sensitized and elicited with DNFB in the daytime or at night. RESULTS: In mice, a nocturnally active animal, we found that ear swelling increased when mice were sensitized at night compared with in the daytime. In addition, cell proliferation and cytokine production in the draining lymph nodes (LNs) were promoted when sensitized at night. We hypothesized that these differences were due to the oscillation of leukocyte distribution in the body through the circadian production of adrenergic hormones. Administration of a β2-adrenergic receptor (β2AR) agonist salbutamol in the daytime decreased the number of immune cells in blood and increased the number of immune cells in LNs. In contrast, a β2AR antagonist ICI18551 administration at night increased the number of immune cells in blood and decreased the number of immune cells in LNs. Accordingly, the severity of CHS response was exacerbated by salbutamol administration in the daytime and attenuated by ICI18551 administration at night. CONCLUSION: Our study demonstrated that the magnitude of adaptive CHS response depends on the circadian rhythm and this knowledge may improve the management of allergic contact dermatitis (ACD) in humans.

リンク情報
DOI
https://doi.org/10.1111/all.15314
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/35426135
ID情報
  • DOI : 10.1111/all.15314
  • PubMed ID : 35426135

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