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Updated: Sep 19, 2025

In Vitro Differentiation of Human CD4+FOXP3+ Induced Regulatory T Cells (iTregs) from Naïve CD4+ T Cells Using a TGF-β-containing Protocol
Published on: December 30, 2016
Thymically imprinted heterogeneity results in differential Treg induction and stability of effector identity
Nathan D Pennock1, Yamin Qian2, Kazumi Ishihara2
1Department of Radiation Medicine, Oregon Health & Science University, Portland, OR 97239, USA.
Abstract:
Thymic selection predisposes naive T cells to particular outcomes when challenged later with cognate antigen, whether the antigen is self or foreign. This suggests that there is an inherent heterogeneity of functioning among T cells within the naive population (both CD4 and CD8), and that each T cell, as part of its thymic development, is given a certain "programming" that will affect its eventual fate decisions. In this project, we looked at the primary effects of this thymic imprinting on the conversion of naive CD4 T cells into Tregs. Furthermore, using an induced-Treg-reporter system, we examine the impact of thymic imprinted heterogeneity on effector functionality and identity stability. We report that naive T cell differential responsivity to cytokines leads to the observed difference in Treg induction and that the Tregs induced from T cells of different self-affinities maintain a heterogeneity of effector function and identity.
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