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Publication : Interleukin-2-Dependent Allergen-Specific Tissue-Resident Memory Cells Drive Asthma.

First Author  Hondowicz BD Year  2016
Journal  Immunity Volume  44
Issue  1 Pages  155-166
PubMed ID  26750312 Mgi Jnum  J:257988
Mgi Id  MGI:6112143 Doi  10.1016/j.immuni.2015.11.004
Citation  Hondowicz BD, et al. (2016) Interleukin-2-Dependent Allergen-Specific Tissue-Resident Memory Cells Drive Asthma. Immunity 44(1):155-166
abstractText  Exposure to inhaled allergens generates T helper 2 (Th2) CD4(+) T cells that contribute to episodes of inflammation associated with asthma. Little is known about allergen-specific Th2 memory cells and their contribution to airway inflammation. We generated reagents to understand how endogenous CD4(+) T cells specific for a house dust mite (HDM) allergen form and function. After allergen exposure, HDM-specific memory cells persisted as central memory cells in the lymphoid organs and tissue-resident memory cells in the lung. Experimental blockade of lymphocyte migration demonstrated that lung-resident cells were sufficient to induce airway hyper-responsiveness, which depended upon CD4(+) T cells. Investigation into the differentiation of pathogenic Trm cells revealed that interleukin-2 (IL-2) signaling was required for residency and directed a program of tissue homing migrational cues. These studies thus identify IL-2-dependent resident Th2 memory cells as drivers of lung allergic responses.
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