PD-1 regulates KLRG1+ group 2 innate lymphoid cells

نویسندگان

  • Samuel Taylor
  • Yuefeng Huang
  • Grace Mallett
  • Chaido Stathopoulou
  • Tania C Felizardo
  • Ming-An Sun
  • Evelyn L Martin
  • Nathaniel Zhu
  • Emma L Woodward
  • Martina S Elias
  • Jonathan Scott
  • Nick J Reynolds
  • William E Paul
  • Daniel H Fowler
  • Shoba Amarnath
چکیده

Group 2 innate lymphoid cells (ILC-2s) regulate immune responses to pathogens and maintain tissue homeostasis in response to cytokines. Positive regulation of ILC-2s through ICOS has been recently elucidated. We demonstrate here that PD-1 is an important negative regulator of KLRG1+ ILC-2 function in both mice and humans. Increase in KLRG1+ ILC-2 cell numbers was attributed to an intrinsic defect in PD-1 signaling, which resulted in enhanced STAT5 activation. During Nippostrongylus brasiliensis infection, a significant expansion of KLRG1+ ILC-2 subsets occurred in Pdcd1-/- mice and, upon adoptive transfer, Pdcd1-/- KLRG1+ ILC-2s significantly reduced worm burden. Furthermore, blocking PD-1 with an antibody increased KLRG1+ ILC-2 cell number and reduced disease burden. Therefore, PD-1 is required for maintaining the number, and hence function, of KLRG1+ ILC-2s.

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منابع مشابه

Immune checkpoints on innate lymphoid cells

In this issue of JEM, Taylor et al. (https ://doi .org /10 .1084 /jem .20161653) describe PD-1 as a critical negative regulator of group 2 innate lymphoid cells (ILC-2s). PD-1 intrinsically controls proliferation and cytokine production of both mouse and human ILC-2s. PD-1 signaling inhibits STAT5 phosphorylation and the removal of this brake by knocking down PD-1 expression or by using anti–PD...

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Immune checkpoints on innate lymphoid cells

In this issue of JEM, Taylor et al. (https ://doi .org /10 .1084 /jem .20161653) describe PD-1 as a critical negative regulator of group 2 innate lymphoid cells (ILC-2s). PD-1 intrinsically controls proliferation and cytokine production of both mouse and human ILC-2s. PD-1 signaling inhibits STAT5 phosphorylation and the removal of this brake by knocking down PD-1 expression or by using anti–PD...

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عنوان ژورنال:

دوره 214  شماره 

صفحات  -

تاریخ انتشار 2017