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Thymus-derived regulatory T cells are positively selected on natural self-antigen through cognate interactions of high functional avidity

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Item Type:Article
Title:Thymus-derived regulatory T cells are positively selected on natural self-antigen through cognate interactions of high functional avidity
Creators Name:Kieback, E., Hilgenberg, E., Stervbo, U., Lampropoulou, V., Shen, P., Bunse, M., Jaimes, Y., Boudinot, P., Radbruch, A., Klemm, U., Kühl, A.A., Liblau, R., Hoevelmeyer, N., Anderton, S.M., Uckert, W. and Fillatreau, S.
Abstract:Regulatory T (Treg) cells expressing Foxp3 transcripton factor are essential for immune homeostasis. They arise in the thymus as a separate lineage from conventional CD4(+)Foxp3(-) T (Tconv) cells. Here, we show that the thymic development of Treg cells depends on the expression of their endogenous cognate self-antigen. The formation of these cells was impaired in mice lacking this self-antigen, while Tconv cell development was not negatively affected. Thymus-derived Treg cells were selected by self-antigens in a specific manner, while autoreactive Tconv cells were produced through degenerate recognition of distinct antigens. These distinct modes of development were associated with the expression of T cell receptor of higher functional avidity for self-antigen by Treg cells than Tconv cells, a difference subsequently essential for the control of autoimmunity. Our study documents how self-antigens define the repertoire of thymus-derived Treg cells to subsequently endow this cell type with the capacity to undermine autoimmune attack.
Keywords:Autoantigens, CTLA-4 Antigen, Cultured Cells, Antigen-Mediated Clonal Selection, Experimental Autoimmune Encephalomyelitis, Forkhead Transcription Factors, Inbred C57BL Mice, Knockout Mice, Multiple Sclerosis, Myelin-Oligodendrocyte Glycoprotein, Peptide Fragments, T-Cell Antigen Receptors, T-Cell Antigen Receptor Specificity, T-Lymphocyte Subsets, Regulatory T-Lymphocytes, Thymus Gland, Animals, Mice
Source:Immunity
ISSN:1074-7613
Publisher:Cell Press / Elsevier
Volume:44
Number:5
Page Range:1114-1126
Date:17 May 2016
Official Publication:https://doi.org/10.1016/j.immuni.2016.04.018
PubMed:View item in PubMed

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