Memory-type ST2⁺CD4⁺ T cells participate in the steroid-resistant pathology of eosinophilic pneumonia.

ABSTRACT: The lung develops an unique epithelial barrier system to protect host from continuous invasion of various harmful particles. Interleukin (IL-)33 released from epithelial cells in the lung drives the type 2 immune response by activating ST2- expressed immune cells in various allergic diseases. However, the involvement of memory-type ST2⁺CD4⁺ T cells in such lung inflammation remains unclear. Here we demonstrated that intratracheal administration of IL-33 resulted in the substantial increase of numbers of tissue-resident memory-type ST2⁺CD4⁺ T cells in the lung. Following enhanced production of IL-5 and IL-13, eosinophilic lung inflammation sequentially developed. IL-33-mediated eosinophilic lung inflammation was not fully developed in T cell-deficient Foxn1 ^nu mice and NSG mice. Dexamethasone treatment showed limited effects on both the cell number and function of memory-type ST2⁺CD4⁺ T cells. Thus our study provides novel insight into the pathogenesis of eosinophilic lung disease, showing that memory-type ST2⁺CD4⁺ T cells are involved in IL-33-induced eosinophilic inflammation and elicited steroid-resistance.

SUBMITTER: Mato N 

PROVIDER: S-EPMC5533714 | biostudies-literature | 2017 Jul

REPOSITORIES: biostudies-literature