Kim Juyang, Kim Hye J, Choi Woon S, Nam Seok H, Cho Hong R, Kwon Byungsuk
The Immunomodulation Research Center, University of Ulsan, Ulsan 680-749, Korea.
Exp Mol Med. 2006 Oct 31;38(5):494-501. doi: 10.1038/emm.2006.58.
In a murine model of systemic lupus erythematosus (SLE)-like chronic graft-versus-host disease (cGVHD), donor CD8+ T cells rapidly fall into anergy to host cells, while donor CD4+ T cells hyperactivate B cells and break B-cell tolerance to self-Ags in the recipient mouse. The functional recovery of donor CD8+ T cells can result in the conversion of cGVHD to acute GVHD (aGVHD), indicating that donor CD8+ T-cell anergy is a restriction factor in the development of cGVHD. In this report, we present evidence that donor CD4+CD25+ regulatory T cells (Treg cells) are critical in maintaining the donor CD8+ T-cell anergy and thus suppressing the development of aGVHD in mice that are naturally prone to cGVHD. Our results provide a novel insight into the role of Treg cells in determining cGVHD versus aGVHD.
在系统性红斑狼疮(SLE)样慢性移植物抗宿主病(cGVHD)的小鼠模型中,供体CD8⁺ T细胞迅速对宿主细胞产生无反应性,而供体CD4⁺ T细胞过度激活B细胞并打破受体小鼠中B细胞对自身抗原的耐受性。供体CD8⁺ T细胞的功能恢复可导致cGVHD转化为急性移植物抗宿主病(aGVHD),这表明供体CD8⁺ T细胞无反应性是cGVHD发展中的一个限制因素。在本报告中,我们提供证据表明,供体CD4⁺CD25⁺调节性T细胞(Treg细胞)对于维持供体CD8⁺ T细胞无反应性并因此抑制天然易患cGVHD的小鼠中aGVHD的发展至关重要。我们的结果为Treg细胞在决定cGVHD与aGVHD中的作用提供了新的见解。