免疫系统
免疫学
背景(考古学)
自身免疫性疾病
白细胞介素17
T细胞
调节性T细胞
免疫耐受
生物
医学
白细胞介素2受体
抗体
古生物学
作者
Yeshuang Yuan,Antonios G.A. Kolios,Yudong Liu,Bo Zhang,Hao Li,George C. Tsokos,Xuan Zhang
标识
DOI:10.1016/j.molmed.2022.04.010
摘要
Autoimmune diseases are characterized by dysregulation and aberrant activation of cells in the immune system. Therefore, restoration of the immune balance represents a promising therapeutic target in autoimmune diseases. Interleukin-2 (IL-2) can promote the expansion and differentiation of different immune cell subsets dose-dependently. At high doses, IL-2 can promote the differentiation and expansion of effector and memory T cells, whereas at low doses, IL-2 can promote the differentiation, survival, and function of regulatory T (Treg) cells, a CD4+ T cell subset that is essential for the maintenance of immune homeostasis and immune tolerance. Therefore, IL-2 exerts immunostimulatory and immunosuppressive effects in autoimmune diseases. The immunoregulatory role of low-dose IL-2 has sparked excitement for the therapeutic exploration of modulating the IL-2-Treg axis in the context of autoimmune diseases. In this review, we discuss recent advances in the therapeutic potential of IL-2 or IL-2-derived molecules in the treatment of autoimmune diseases.
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