T helper (Th) 17 cells protect from infections and are pathogenic in autoimmunity. While human Th17 cell differentiation has been defined, the global and stepwise transcriptional changes accompanying this process remain uncharacterized. Herein, by performing transcriptome analysis of human Th17 cells, we uncovered three time-regulated modules: early, involving exclusively "signaling pathways" genes; late, characterized by response to infections; and persistent, involving effector immune functions. To assign them an inflammatory or regulatory potential, we compared Th17 cells differentiated in presence or absence of interleukin (IL)-1β, respectively. Most inflammatory genes belong to the persistent module, whereas regulatory genes are lately or persistently induced. Among inflammatory genes, we identified the effector molecules IL17A, IL17F, IL26, IL6, interferon (IFN)G, IFNK, LTA, IL1A, platelet-derived growth factor (PDGF) A and the transcriptional regulators homeodomain-only protein homeobox (HOPX) and sex-determining-region-Y-box (SOX)2, whose expression was independently validated. This study provides an integrative representation of the stepwise human Th17 differentiation program and offers new perspectives toward therapeutic targeting of Th17-related autoimmune diseases.

Capone, A., Naro, C., Bianco, M., De Bardi, M., Noël, F., Macchi, P., Battistini, L., Soumelis, V., Volpe, E., Sette, C., Systems analysis of human T helper17 cell differentiation uncovers distinct time-regulated transcriptional modules, <<ISCIENCE>>, 2021; (24): 1-14. [doi:10.1016/j.isci.2021.102492] [http://hdl.handle.net/10807/189521]

Systems analysis of human T helper17 cell differentiation uncovers distinct time-regulated transcriptional modules

Naro, Chiara
Secondo
;
Sette, Claudio
Ultimo
2021

Abstract

T helper (Th) 17 cells protect from infections and are pathogenic in autoimmunity. While human Th17 cell differentiation has been defined, the global and stepwise transcriptional changes accompanying this process remain uncharacterized. Herein, by performing transcriptome analysis of human Th17 cells, we uncovered three time-regulated modules: early, involving exclusively "signaling pathways" genes; late, characterized by response to infections; and persistent, involving effector immune functions. To assign them an inflammatory or regulatory potential, we compared Th17 cells differentiated in presence or absence of interleukin (IL)-1β, respectively. Most inflammatory genes belong to the persistent module, whereas regulatory genes are lately or persistently induced. Among inflammatory genes, we identified the effector molecules IL17A, IL17F, IL26, IL6, interferon (IFN)G, IFNK, LTA, IL1A, platelet-derived growth factor (PDGF) A and the transcriptional regulators homeodomain-only protein homeobox (HOPX) and sex-determining-region-Y-box (SOX)2, whose expression was independently validated. This study provides an integrative representation of the stepwise human Th17 differentiation program and offers new perspectives toward therapeutic targeting of Th17-related autoimmune diseases.
Inglese
Capone, A., Naro, C., Bianco, M., De Bardi, M., Noël, F., Macchi, P., Battistini, L., Soumelis, V., Volpe, E., Sette, C., Systems analysis of human T helper17 cell differentiation uncovers distinct time-regulated transcriptional modules, <<ISCIENCE>>, 2021; (24): 1-14. [doi:10.1016/j.isci.2021.102492] [http://hdl.handle.net/10807/189521]
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