Kyewski Bruno, Derbinski Jens
Tumour Immunology Programme, Division of Developmental Immunology, German Cancer Research Centre, Im Neuenheimer Feld 280, D-69120, Heidelberg, Germany.
Nat Rev Immunol. 2004 Sep;4(9):688-98. doi: 10.1038/nri1436.
The thymus has been viewed as the main site of tolerance induction to self-antigens that are specifically expressed by thymic cells and abundant blood-borne self-antigens, whereas tolerance to tissue-restricted self-antigens has been ascribed to extrathymic (peripheral) tolerance mechanisms. However, the phenomenon of promiscuous expression of tissue-restricted self-antigens by medullary thymic epithelial cells has led to a reassessment of the role of central T-cell tolerance in preventing organ-specific autoimmunity. Recent evidence indicates that both genetic and epigenetic mechanisms account for this unorthodox mode of gene expression. As we discuss here, these new insights have implications for our understanding of self-tolerance in humans, its breakdown in autoimmune diseases and the significance of this tolerance mode in vertebrate evolution.
胸腺一直被视为对胸腺细胞特异性表达的自身抗原以及丰富的血源性自身抗原进行耐受诱导的主要场所,而对组织限制性自身抗原的耐受则归因于胸腺外(外周)耐受机制。然而,髓质胸腺上皮细胞对组织限制性自身抗原的杂乱表达现象,促使人们重新评估中枢T细胞耐受在预防器官特异性自身免疫中的作用。最近的证据表明,遗传和表观遗传机制都能解释这种非传统的基因表达模式。正如我们在此所讨论的,这些新见解对我们理解人类的自身耐受、其在自身免疫性疾病中的破坏以及这种耐受模式在脊椎动物进化中的意义都有影响。