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Updated: May 19, 2026

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
You, me and Foxp3: immune regulation for two
Andy Tsun1, Yang Yang Li, Bin Li
1Key Laboratory of Molecular Virology & Immunology, Unit of Molecular Immunology, Institut Pasteur of Shanghai, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 411 Hefei Road (South), Shanghai, 200025, China.
Abstract:
Forkhead Box P3 (Foxp3) is a lineage-specific transcription factor that controls the differentiation of CD4(+) regulatory T cells. The expression of Foxp3 in regulatory T cells is crucial for the upregulation of immunosuppressive effector molecules, whereby Foxp3 disruption leads to the breakdown of immune tolerance and the development of autoimmune disease. The present study reveals how CD11b(+) F4/80(+) macrophages also express Foxp3; it is not solely restricted to T cells in the immune system. The expression of Foxp3 in CD11b(+) F4/80(+) macrophages endows them with immunosuppressive ability. Foxp3(+) macrophages were subjected to global gene expression and proteomic analyses to reveal their unique profile, demonstrating how the mode by which Foxp3(+) macrophages exert their function involves the upregulation of immunoregulatory pathways. This finding indicates that Foxp3 is more widely expressed in the immune cells than previously thought.
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