Hall Bruce M
Immune Tolerance Laboratory, Department of Medicine, University of New South Wales, Sydney, Australia; and Renal Unit, Liverpool Hospital, Sydney, Australia
Clin J Am Soc Nephrol. 2015 Nov 6;10(11):2050-64. doi: 10.2215/CJN.06620714. Epub 2015 Apr 15.
Traditionally, T cells were CD4+ helper or CD8+ cytotoxic T cells, and with antibodies, they were the soldiers of immunity. Now, many functionally distinct subsets of activated CD4+ and CD8+ T cells have been described, each with distinct cytokine and transcription factor expression. For CD4+ T cells, these include Th1 cells expressing the transcription factor T-bet and cytokines IL-2, IFN-γ, and TNF-β; Th2 cells expressing GATA-3 and the cytokines IL-4, IL-5, and IL-13; and Th17 cells expressing RORγt and cytokines IL-17A, IL-17F, IL-21, and IL-22. The cytokines produced determine the immune inflammation that they mediate. T cells of the effector lineage can be naïve T cells, recently activated T cells, or memory T cells that can be distinguished by cell surface markers. T regulatory cells or spies were characterized as CD8+ T cells expressing I-J in the 1970s. In the 1980s, suppressor cells fell into disrepute when the gene for I-J was not present in the mouse MHC I region. At that time, a CD4+ T cell expressing CD25, the IL-2 receptor-α, was identified to transfer transplant tolerance. This was the same phenotype of activated CD4+ CD25+ T cells that mediated rejection. Thus, the cells that could induce tolerance and undermine rejection had similar badges and uniforms as the cells effecting rejection. Later, FOXP3, a transcription factor that confers suppressor function, was described and distinguishes T regulatory cells from effector T cells. Many subtypes of T regulatory cells can be characterized by different expressions of cytokines and receptors for cytokines or chemokines. In intense immune inflammation, T regulatory cells express cytokines characteristic of effector cells; for example, Th1-like T regulatory cells express T-bet, and IFN-γ-like Th1 cells and effector T cells can change sides by converting to T regulatory cells. Effector T cells and T regulatory cells use similar molecules to be activated and mediate their function, and thus, it can be very difficult to distinguish soldiers from spies.
传统上,T细胞是CD4+辅助性T细胞或CD8+细胞毒性T细胞,借助抗体,它们是免疫的战士。如今,已描述了许多功能不同的活化CD4+和CD8+ T细胞亚群,每个亚群都有独特的细胞因子和转录因子表达。对于CD4+ T细胞,这些包括表达转录因子T-bet以及细胞因子IL-2、IFN-γ和TNF-β的Th1细胞;表达GATA-3以及细胞因子IL-4、IL-5和IL-13的Th2细胞;以及表达RORγt和细胞因子IL-17A、IL-17F、IL-21和IL-22的Th17细胞。所产生的细胞因子决定了它们介导的免疫炎症。效应谱系的T细胞可以是初始T细胞、最近活化的T细胞或记忆T细胞,它们可通过细胞表面标志物加以区分。T调节细胞或“间谍”在20世纪70年代被表征为表达I-J的CD8+ T细胞。在20世纪80年代,当I-J基因不在小鼠MHC I区域时,抑制细胞声名扫地。当时,一种表达CD25(IL-2受体-α)的CD4+ T细胞被确定可传递移植耐受性。这与介导排斥反应的活化CD4+ CD25+ T细胞具有相同的表型。因此,能够诱导耐受性并破坏排斥反应的细胞与引发排斥反应的细胞具有相似的标志和特征。后来,一种赋予抑制功能的转录因子FOXP3被描述出来,它将T调节细胞与效应T细胞区分开来。许多T调节细胞亚群可通过细胞因子以及细胞因子或趋化因子受体的不同表达来表征。在强烈的免疫炎症中,T调节细胞表达效应细胞特有的细胞因子;例如,Th1样T调节细胞表达T-bet,而IFN-γ样Th1细胞和效应T细胞可通过转化为T调节细胞而改变立场。效应T细胞和T调节细胞使用相似的分子被激活并介导其功能,因此,区分战士和间谍可能非常困难。