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• W2003936617 abstract "Thymectomy at day 3 after birth leads to autoimmune disease in some genetic backgrounds. Disease is thought to be caused by the lack/paucity of regulatory T cells. We show that 3-day-old mice already contain a significant compartment of Foxp3 -expressing CD25 + CD4 + splenocytes. Whereas, in adult spleen, the subsets of regulatory T cells (CD25 + and/or CD103 + ) express high amounts of Foxp3 mRNA, in 3-day-old mice, both thymic and splenic CD25 + CD4 + T cell subsets express lower amounts of Foxp3 mRNA, and CD103 + cells are barely detected. In adult day 3-thymectomized mice, the CD25 + CD4 + T cell subset is overrepresented (most of the cells being CD103 + ) and expresses high amounts of Foxp3 mRNA, independent of the development of autoimmune gastritis. These cells control inflammatory bowel disease and the homeostatic expansion of lymphocytes. This study demonstrates that the peripheral immune system of newborn mice is endowed of a remarkable regulatory potential, which develops considerably in the absence of thymic supply." @default.
• W2003936617 created "2016-06-24" @default.
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• W2003936617 date "2004-09-27" @default.
• W2003936617 modified "2023-10-14" @default.
• W2003936617 title "Regulatory potential and control of<i>Foxp3</i>expression in newborn CD4⁺T cells" @default.
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• W2003936617 doi "https://doi.org/10.1073/pnas.0403303101" @default.
• W2003936617 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/521951" @default.
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