中心公差
周边公差
生物
免疫耐受
克隆缺失
免疫系统
免疫学
T细胞
否定选择
调节性T细胞
细胞生物学
白细胞介素2受体
T细胞受体
基因
生物化学
基因组
作者
Thea Magrone,Emilio Jirillo
出处
期刊:Endocrine, metabolic & immune disorders
[Bentham Science Publishers]
日期:2019-06-03
卷期号:19 (5): 580-593
被引量:3
标识
DOI:10.2174/1871530319666181211161721
摘要
Background: T cell tolerance both at thymic and peripheral levels is a mechanism of protection finalized to eradicate autoreactive T cell clones and/or to maintain immune homeostasis, especially, postnatally. Central tolerance occurs in the thymic medulla via a mechanism of negative selection which leads to the eradication of autoreactive T cell clones. Mechanisms of Action: Such a tolerogenic event relies on Fas-mediated apoptosis of autoreactive T cell clones operated by thymic dendritic cells (DCs), on the one hand. On the other hand, activated thymic T regulatory (Treg) cells in cooperation with medullary thymic epithelial cells and DCs suppress autoreactive T cell clones. Peripherally, different types of Treg cells exert the so-called peripheral tolerance towards autoreactive T cell clones which may have escaped from negative selection mechanisms. At the same time, peripheral Treg cells activated by tolerogenic DC have antiinflammatory activities, especially in the intestine towards food and microbial antigens. Drug Targeting: Various natural and dietary products, such as vitamins (A, C, D), lactobacilli and polyphenols will be described for their tolerogenic capacity to attenuate the inflammatory pathway, as observed in preclinical and clinical studies.
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