生物
免疫系统
炎症
FOXP3型
免疫学
细胞生物学
机制(生物学)
转录因子
调节性T细胞
细胞分化
T细胞
获得性免疫系统
白细胞介素2受体
遗传学
基因
哲学
认识论
作者
Steven Z. Josefowicz,Li‐Fan Lu,Alexander Y. Rudensky
标识
DOI:10.1146/annurev.immunol.25.022106.141623
摘要
The immune system has evolved to mount an effective defense against pathogens and to minimize deleterious immune-mediated inflammation caused by commensal microorganisms, immune responses against self and environmental antigens, and metabolic inflammatory disorders. Regulatory T (Treg) cell-mediated suppression serves as a vital mechanism of negative regulation of immune-mediated inflammation and features prominently in autoimmune and autoinflammatory disorders, allergy, acute and chronic infections, cancer, and metabolic inflammation. The discovery that Foxp3 is the transcription factor that specifies the Treg cell lineage facilitated recent progress in understanding the biology of regulatory T cells. In this review, we discuss cellular and molecular mechanisms in the differentiation and function of these cells.
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