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Mast cell-mediated hypersensitivity to fluoroquinolone is MRGPRX2 dependent

  • Rui Liu
  • , Shiling Hu
  • , Yongjing Zhang
  • , Delu Che
  • , Jiao Cao
  • , Jue Wang
  • , Tingting Zhao
  • , Qianqian Jia
  • , Nan Wang
  • , Tao Zhang

Research output: Contribution to journalArticlepeer-review

54 Scopus citations

Abstract

Fluoroquinolones trigger anaphylaxis during clinical applications, affecting the safety of their administration. Mast cells are immune cells that act as sentinels during host defenses, mediating hypersensitivity and anaphylactic reactions. Mas-related G protein-coupled receptor X2 (MRGPRX2) is a mast cell-specific receptor that mediates cell degranulation in anaphylactic reactions. In this study, the mechanism underpinning the anaphylactic reactions caused by fluoroquinolones was investigated. Hypersensitivity was assessed through hindpaw swelling, tissue fluid leakage assays, in vivo and body temperature measurements assay in vivo, and cell calcium mobilization assays, and mast cell degranulation assays in vitro. Mast cell-deficient W-sash c-kit mutant Kit W-sh/W-sh mice and MrgprB2 (the orthologous receptor of MRGPRX2 in mice) knockout mice exhibited reduced fluoroquinolone-induced anaphylactic effects. Fluoroquinolones activated mast cells in a dose-dependent manner and reduced degranulation was observed following MRGPRX2 silencing. These results reveal that fluoroquinolone-induced anaphylactic reactions are mediated by mast cells through MRGPRX2.

Original languageEnglish
Pages (from-to)417-427
Number of pages11
JournalInternational Immunopharmacology
Volume70
DOIs
StatePublished - May 2019

Keywords

  • Anaphylaxis
  • Degranulation
  • Fluoroquinolones
  • MRGPRX2
  • Mast cell

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