免疫学
免疫系统
炎症
生物
先天性淋巴细胞
调节性B细胞
过敏性炎症
免疫耐受
调节性T细胞
微生物群
FOXP3型
免疫
T细胞
白细胞介素10
白细胞介素2受体
遗传学
作者
Min-Jhen Jheng,Hirohito Kita
摘要
<b><i>Background:</i></b> Epithelial barriers, such as the lungs and skin, face the challenge of providing the tissues’ physiological function and maintaining tolerance to the commensal microbiome and innocuous environmental factors while defending the host against infectious microbes. Asthma and allergic diseases can result from maladaptive immune responses, resulting in exaggerated and persistent type 2 immunity and tissue inflammation. <b><i>Summary:</i></b> Among the diverse populations of tissue immune cells, CD4<sup>+</sup> regulatory T cells (Treg cells) are central to controlling immune responses and inflammation and restoring tissue homeostasis. Humans and mice that are deficient in Treg cells experience extensive inflammation in their mucosal organs and skin. During past decades, major progress has been made toward understanding the immunobiology of Treg cells and the molecular and cellular mechanisms that control their differentiation and function. It is now clear that Treg cells are not a single cell type and that they demonstrate diversity and plasticity depending on their differentiation stages and tissue environment. They could also take on a proinflammatory phenotype in certain conditions. <b><i>Key Messages:</i></b> Treg cells perform distinct functions, including the induction of immune tolerance, suppression of inflammation, and promotion of tissue repair. Subsets of Treg cells in mucosal tissues are regulated by their differentiation stage and tissue inflammatory milieu. Treg cell dysfunction likely plays roles in persistent immune responses and tissue inflammation in asthma and allergic diseases.
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