Memory regulatory T cells reside in human skin. This model provides a rationale for inflammation IL-4 and IL-6 induced downregulation of Foxp3 in Treg cells and IL-2 dependent counteraction of this process. Crumb R. Moreover, depletion of Treg cells prior to or after onset of experimental autoimmune encephalomyelitis EAE worsens the disease and prevents recovery 10 — It is an intriguing concept to exploit Treg cells for therapeutic interventions—either enhancing their function in autoimmunity or dampening their effect in cancer.
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Pauli. Thomas Korn1,2,3* and Andreas Muschaweckh1,2 . The majority of human peripheral blood CD4+CD25highFoxp3+ regulatory T cells bear functional Huehn J, Polansky JK, Hamann A.
Epigenetic control of FOXP3. Sanchez Rodriguez R, Pauli ML, Neuhaus IM, Yu SS, Arron ST, Harris HW, et al.
While Treg cells are recruited to sites of inflammation in order to resolve inflammation and re-establish appropriate organ function, it is increasingly recognized that a series of inflammatory but also non-inflammatory perturbations of organ function lead to the constitution of relatively long lived populations of Treg cells in NLTs.
Cell Metab. Sci Transl Med.
TK conceptualized and wrote the review. Control of tissue-localized immune responses by human regulatory T cells.
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Rather, more tailored strategies to either selectively expand subsets of Treg cells or to instruct them to adopt appropriate organ-specific features might have to be developed.
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Nat Rev Genet. The transcription factors Blimp-1 and IRF4 jointly control the differentiation and function of effector regulatory T cells. Eur J Immunol.
Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases. Cell Metab. Here, direct transactivators of Foxp3 as well as transcriptional inhibitors of effector T cell programs have been described Table 1. Regulatory T cells are key cerebroprotective immunomodulators in acute experimental stroke.
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|Extrathymically generated regulatory T cells control mucosal TH2 inflammation.
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Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains CD The use, distribution or reproduction in other forums is permitted, provided the original author s and the copyright owner s are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. Treg cells in secondary lymphoid tissues are indispensable for maintaining immune tolerance because elimination of Treg cells either in newborn individuals or in adults results in multiorgan autoimmunity within a couple of weeks 23.
Interestingly, Treg cell numbers remain elevated in the post-EAE central nervous system for a prolonged period of time, raising the question of whether these cells might also play a significant role in promoting tissue repair in the recovering central nervous system.