The differentiation of helper T cell subsets is influenced by a diversity of microRNAs. In the Proceedings of the National Academy of Sciences USA, Wilson and colleagues use a comprehensive transcriptomics approach to identify microRNA signatures associated with the TH1, TH2, TH17 and induced regulatory T cell subsets in vitro and in vivo. TH2 cells generated in vivo have a miRNA profile clearly distinguishable from that of other subsets and, unexpectedly, also show very little overlap with their TH2 counterparts generated in vitro. In particular, the microRNAs miR-155 and miR-146a are dynamically regulated in TH2 cells generated in vivo, with the former promoting and the latter regulating effector function in a cell-intrinsic manner. miR-155 regulates expression of the S1P1 receptor for the bioactive lipid S1P and may therefore exert its effects in part by controlling migration to sites of tissue inflammation. Targeting miR-155 may therefore alleviate type 2 pathologies such as allergy.

PNAS (14 July 2014) doi:10.1073/pnas.1406322111