<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE320nnn/GSE320556/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE320556</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>TGF-beta promotes human T follicular helper cell stemness properties at the expense of effector function</name><description>Follicular helper T (TFH) cells are essential for germinal center reactions and the maintenance of long-lived humoral immunity. Transforming growth factor-β (TGF-β) is a multifunctional cytokine implicated in immune regulation, T-cell differentiation, and the maintenance of cellular stemness. Prior studies have shown that TGF-β promotes stemness across a wide range of cell types and facilitates the differentiation of naïve CD4⁺ T cells into various T helper cell subsets. However, its precise effects on TFH effector function and stem-like properties remain poorly understood. Here, the dual regulatory roles of TGF-β1 in modulating TFH effector functions and stem-like properties were investigated. We found that TGF-β1 treatment in vitro promoted human naïve CD4+ T cells differentiation into CXCR3⁺ TFH, but significantly attenuated their effector molecule expression and TFH-mediated memory B-cell differentiation and antibody production, whereas it enhanced the expression of stemness-associated molecules in TFH cells both differentiated in vitro from naïve CD4+ T cells and isolated from blood. Notably, TGF-β1 promoted proliferation and reduced apoptosis of naïve-derived TFH cells in vitro, but suppressed proliferation and increased early apoptosis in blood-derived mature TFH cells. Collectively, these findings indicate that TGF-β1 tunes the balance between TFH effector function and stem-like properties, and show differential regulations of the early phase of TFH differentiation and mature TFH cells, which may have implications for TFH-driven immune pathology and disease.</description><dates><publication>2026/04/15</publication></dates><accession>GSE320556</accession><cross_references><GSM>GSM9545671</GSM><GSM>GSM9545672</GSM><GSM>GSM9545680</GSM><GSM>GSM9545670</GSM><GSM>GSM9545675</GSM><GSM>GSM9545676</GSM><GSM>GSM9545673</GSM><GSM>GSM9545674</GSM><GSM>GSM9545679</GSM><GSM>GSM9545669</GSM><GSM>GSM9545677</GSM><GSM>GSM9545678</GSM><GPL>16791</GPL><GSE>320556</GSE><taxon>Homo sapiens</taxon><PMID>[41958642]</PMID></cross_references></HashMap>