Abstract / Description of output
CD4+ T cells have long been grouped into distinct helper subsets on the basis of their cytokine-secretion profile. In recent years, several subsets of innate lymphoid cell have been described as key producers of these same Th-associated cytokines. However, the functional relationship between Th cells and innate lymphoid cells (ILCs) remains unclear. We show in this study that lineage-negative ST2+ICOS+CD45+ type 2 ILCs and CD4+ T cells can potently stimulate each other’s function via distinct mechanisms. CD4+ T cell provision of IL-2 stimulates type 2 cytokine production by type 2 ILCs. By contrast, type 2 ILCs modulate naive T cell activation in a cell contact–dependent manner, favoring Th2 while suppressing Th1 differentiation. Furthermore, a proportion of type 2 ILCs express MHC class II and can present peptide Ag in vitro. Importantly, cotransfer experiments show that type 2 ILCs also can boost CD4+ T cell responses to Ag in vivo.
Original language | English |
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Pages (from-to) | 2442-2448 |
Number of pages | 7 |
Journal | The Journal of Immunology |
Volume | 192 |
Issue number | 5 |
Early online date | 27 Jan 2014 |
DOIs | |
Publication status | Published - 1 Mar 2014 |
Keywords / Materials (for Non-textual outputs)
- Animals
- Antigens, Differentiation
- Cell Differentiation
- Cytokines
- Histocompatibility Antigens Class II
- Immunity, Innate
- Mice
- Mice, Inbred BALB C
- Mice, Knockout
- Th1 Cells
- Th2 Cells
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Ananda Mirchandani
- Deanery of Clinical Sciences - Senior Clinical Research Fellow in Respiratory Medicine
- Centre for Inflammation Research
Person: Academic: Research Active