Morel P A, Oriss T B
Department of Medicine, University of Pittsburgh, PA, USA.
Crit Rev Immunol. 1998;18(4):275-303. doi: 10.1615/critrevimmunol.v18.i4.10.
Th1 and Th2 subsets have been characterized on the basis of the cytokines they secrete and the immune functions they mediate. Th1 cells secrete IL-2, IFN-gamma, and lymphotoxin and are important in the cell-mediated response; Th2 cells secrete IL-4, IL-5, IL-10, and IL-13 and are important in the control of macrophage function and in the stimulation of particular immunoglobulin isotypes. Cytokines secreted by Th1 and Th2 cells regulate the growth and differentiation of Th1 and Th2 cells in both positive and negative ways; this has been termed crossregulation. Much work has concentrated on the factors important in the differentiation of these Th subsets, and it has been established that Th cells become committed to a Th1 or Th2 phenotype within 48 hrs of antigenic stimulation. During the differentiation process irreversible changes in the expression and function of cytokine receptors occur that provide an explanation for the observed crossregulatory features of Th1 and Th2 cells. In this review we summarize the crossregulation between Th1 and Th2 cells in terms of the changes in cytokine receptor expression and function that occur during differentiation.
Th1和Th2亚群是根据它们分泌的细胞因子和介导的免疫功能来界定的。Th1细胞分泌白细胞介素-2(IL-2)、γ干扰素(IFN-γ)和淋巴毒素,在细胞介导的反应中起重要作用;Th2细胞分泌IL-4、IL-5、IL-10和IL-13,在控制巨噬细胞功能和刺激特定免疫球蛋白同种型方面起重要作用。Th1和Th2细胞分泌的细胞因子以正负两种方式调节Th1和Th2细胞的生长和分化;这被称为交叉调节。许多工作都集中在这些Th亚群分化过程中的重要因素上,并且已经确定Th细胞在抗原刺激后48小时内就会定向分化为Th1或Th2表型。在分化过程中,细胞因子受体的表达和功能会发生不可逆的变化,这为观察到的Th1和Th2细胞的交叉调节特性提供了解释。在这篇综述中,我们根据分化过程中细胞因子受体表达和功能的变化,总结了Th1和Th2细胞之间的交叉调节。