| Literature DB >> 26287681 |
Jonathan M Coquet1, Martijn J Schuijs2, Mark J Smyth3, Kim Deswarte2, Rudi Beyaert4, Harald Braun4, Louis Boon5, Gunilla B Karlsson Hedestam6, Steven L Nutt7, Hamida Hammad8, Bart N Lambrecht9.
Abstract
Asthma is a T helper 2 (Th2)-cell-mediated disease; however, recent findings implicate Th17 and innate lymphoid cells also in regulating airway inflammation. Herein, we have demonstrated profound interleukin-21 (IL-21) production after house dust mite (HDM)-driven asthma by using T cell receptor (TCR) transgenic mice reactive to Dermatophagoides pteronyssinus 1 and an IL-21GFP reporter mouse. IL-21-producing cells in the mediastinal lymph node (mLN) bore characteristics of T follicular helper (Tfh) cells, whereas IL-21(+) cells in the lung did not express CXCR5 (a chemokine receptor expressed by Tfh cells) and were distinct from effector Th2 or Th17 cells. Il21r(-/-) mice developed reduced type 2 responses and the IL-21 receptor (IL-21R) enhanced Th2 cell function in a cell-intrinsic manner. Finally, administration of recombinant IL-21 and IL-25 synergistically promoted airway eosinophilia primarily via effects on CD4(+) lymphocytes. This highlights an important Th2-cell-amplifying function of IL-21-producing CD4(+) T cells in allergic airway inflammation.Entities:
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Year: 2015 PMID: 26287681 DOI: 10.1016/j.immuni.2015.07.015
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745