Saxena Amit, Bauer Jan, Scheikl Tanja, Zappulla Jacques, Audebert Marc, Desbois Sabine, Waisman Ari, Lassmann Hans, Liblau Roland S, Mars Lennart T
Institut National de la Santé et de la Recherche Médicale, Unité 563, Toulouse, France.
J Immunol. 2008 Aug 1;181(3):1617-21. doi: 10.4049/jimmunol.181.3.1617.
CD8 T cells are emerging as important players in multiple sclerosis (MS) pathogenesis, although their direct contribution to tissue damage is still debated. To assess whether autoreactive CD8 T cells can contribute to the pronounced loss of oligodendrocytes observed in MS plaques, we generated mice in which the model Ag influenza hemagglutinin is selectively expressed in oligodendrocytes. Transfer of preactivated hemagglutinin-specific CD8 T cells led to inflammatory lesions in the optic nerve, spinal cord, and brain. These lesions, associating CD8 T cell infiltration with focal loss of oligodendrocytes, demyelination, and microglia activation, were very reminiscent of active MS lesions. Thus, our study demonstrates the potential of CD8 T cells to induce oligodendrocyte lysis in vivo as a likely consequence of direct Ag-recognition. These results provide new insights with regard to CNS tissue damage mediated by CD8 T cells and for understanding the role of CD8 T cells in MS.
CD8 T细胞正在成为多发性硬化症(MS)发病机制中的重要参与者,尽管它们对组织损伤的直接作用仍存在争议。为了评估自身反应性CD8 T细胞是否会导致MS斑块中明显的少突胶质细胞丢失,我们构建了在少突胶质细胞中选择性表达模型抗原流感血凝素的小鼠。预激活的血凝素特异性CD8 T细胞的转移导致视神经、脊髓和大脑出现炎性病变。这些病变伴有CD8 T细胞浸润以及少突胶质细胞局灶性丢失、脱髓鞘和小胶质细胞激活,与活动性MS病变非常相似。因此,我们的研究证明了CD8 T细胞在体内诱导少突胶质细胞裂解的可能性,这可能是直接抗原识别的结果。这些结果为CD8 T细胞介导的中枢神经系统组织损伤以及理解CD8 T细胞在MS中的作用提供了新的见解。