Aire regulates negative selection of organ-specific T cells
By A. Liston, S. Lesage, Judith Wilson, L. Peltonen, C. Goodnow. Nature Immunology, 2003
831 citations recorded by the source corpus.
Subfields: Endocrinology, Diabetes and Metabolism, Genetics, Immunology
View Paper: https://www.semanticscholar.org/paper/85ea3a315dd7c609ab45141896627096932b910e
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In Endocrinology, Diabetes and Metabolism
In Genetics
In Immunology
Citations in the corpus
- Type 1 diabetes: etiology, immunology, and therapeutic strategies. (2011, background): “This reduced expression allows autoreactive T cells to escape into the periphery, because it interferes with thymic deletion (16, 246).”
- Selection of Foxp3+ regulatory T cells specific for self antigen expressed and presented by Aire+ medullary thymic epithelial cells (2007, background): “Evidence suggests that tissue-specific antigens expressed in mTECs contribute to central tolerance in an essential way by inducing recessive tolerance (such as clonal deletion of autoreactive thymocytes”
- Immunity to fungal infections (2011, background): “CMC, although encompassing various clinical entities, has been associated with autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy — a condition in which the mutated gene has been shown to be involved in the ontogeny of CD25 + T Reg cell”
- Central tolerance: learning self-control in the thymus (2005, background): “and that mutations in the gene encoding AIRE underlie a specific human autoimmune disease, APECE”
- The cellular mechanism of Aire control of T cell tolerance. (2005, methodology): “cells were the same in Aire-positive and -negative hen egg lysozyme (HEL)-specific TCR tg mice ( Liston et al., 2003 ).”
- Cellular and genetic mechanisms of self tolerance and autoimmunity (2005, background): “and a marked failure to delete organ-specific TCRs in the thymus because tissue-specific genes are not switched on in rare medullary thymic epithelial cell”
- Foxp3+CD25+CD4+ natural regulatory T cells in dominant self‐tolerance and autoimmune disease (2006, background): “in the medullary epithelial cells, whereas the number and in vitro assessed suppressive activity of natural Tregs are reportedly intact (116, 117).”