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Eosinophil recruitment is dynamically regulated by interplay among lung dendritic cell subsets after allergen challenge.

Shuying YiJing ZhaiRui NiuGuangming ZhuMeixiang WangJianguo LiuHua HuangYaping WangXiuli JingLi KangWengang SongYufang ShiHua Tang
Published in: Nature communications (2018)
Eosinophil infiltration, a hallmark of allergic asthma, is essential for type 2 immune responses. How the initial eosinophil recruitment is regulated by lung dendritic cell (DC) subsets during the memory stage after allergen challenge is unclear. Here, we show that the initial eosinophil infiltration is dependent on lung cDC1s, which require nitric oxide (NO) produced by inducible NO synthase from lung CD24-CD11b+ DC2s for inducing CCL17 and CCL22 to attract eosinophils. During late phase responses after allergen challenge, lung CD24+ cDC2s inhibit eosinophil recruitment through secretion of TGF-β1, which impairs the expression of CCL17 and CCL22. Our data suggest that different lung antigen-presenting cells modulate lung cDC1-mediated eosinophil recruitment dynamically, through secreting distinct soluble factors during the memory stage of chronic asthma after allergen challenge in the mouse.
Keyphrases
  • dendritic cells
  • allergic rhinitis
  • nitric oxide
  • immune response
  • regulatory t cells
  • liver fibrosis
  • poor prognosis
  • cell death
  • oxidative stress
  • cystic fibrosis
  • toll like receptor
  • pi k akt
  • cell cycle arrest