Chang Xing, Zheng Pan, Liu Yang
Division of Immunotherapy, Department of Surgery, Comprehensive Cancer Center and Program of Molecular Mechanism of Diseases, University of Michigan, Ann Arbor, MI 48109, USA.
Clin Immunol. 2009 Jan;130(1):61-73. doi: 10.1016/j.clim.2008.08.014. Epub 2008 Oct 1.
How regulatory T cells (Treg) control autoreactive T cells has not been analyzed in animals with a normal T cell repertoire. Using endogenous viral superantigens (VSAg) as the primary self antigens and mice with the Scurfy mutation of FoxP3, we show here that the Treg defect causes preferential accumulation of autoreactive T cells. Interestingly, in the Scurfy mice, the proliferation of VSAg-reactive T cells was no more vigorous than that of non-VSAg-reactive T cells, which indicated that the preferential accumulation is not due to preferential proliferation. In contrast, VSAg-reactive T cells disappears in WT host despite their preferential proliferation. Importantly, when adoptively transferred into the newborn Scurfy mice, the Treg selectively kill autoreactive T cells without affecting their proliferation. The selective elimination is due to increased susceptibility of autoreactive T cells to Treg-mediated killing.
在具有正常T细胞库的动物中,调节性T细胞(Treg)如何控制自身反应性T细胞尚未得到分析。我们以内源性病毒超抗原(VSAg)作为主要自身抗原,并利用携带FoxP3基因Scurfy突变的小鼠,在此表明Treg缺陷会导致自身反应性T细胞优先积累。有趣的是,在Scurfy小鼠中,VSAg反应性T细胞的增殖并不比非VSAg反应性T细胞更活跃,这表明优先积累并非由于优先增殖。相反,尽管VSAg反应性T细胞优先增殖,但它们在野生型宿主中会消失。重要的是,当将Treg过继转移到新生Scurfy小鼠中时,Treg会选择性地杀死自身反应性T细胞,而不影响其增殖。这种选择性清除是由于自身反应性T细胞对Treg介导的杀伤作用的敏感性增加。