Department of Neurology, Martin-Luther-University, Halle (Saale), Germany.
Cell Immunol. 2010;264(1):93-6. doi: 10.1016/j.cellimm.2010.05.003. Epub 2010 May 11.
In the present investigation, T-cell subsets of the previously described superantigen-induced encephalitis [9] have been investigated in 16 Lewis rats in comparison with four controls. Three days after intracerebral injection of Staphylococcal Enterotoxin A (SEA) or saline, 1.5 x 10(7) ConA-activated splenocytes were loaded i.v. animals were sacrificed after 0.5, 3 or 5 days, followed by immunohistochemical investigation of CD3, CD4 and CD8. Pronounced perivascular cuffing was identified 0.5 days after splenocyte injection and declined thereafter. The majority of the perivascular round cells consisted of CD8+ T-cells (65%) and CD4+ T-cells (10%). Less than 20% of the perivascular round cells were CD3+. The reduced expression of CD3 relative to e.g. CD8 is presumably due to the previous superantigenic stimulus. The presented data may be of relevance for the pathogenesis of infectious or autoimmune encephalitis, e.g. in multiple sclerosis.
在本研究中,我们比较了 16 只 Lewis 大鼠和 4 只对照鼠,对先前描述的超抗原诱导性脑炎[9]中的 T 细胞亚群进行了研究。在 SEA 或生理盐水脑内注射 3 天后,静脉内负载 1.5 x 10(7)ConA 激活的脾细胞。在 0.5、3 或 5 天后处死动物,然后进行 CD3、CD4 和 CD8 的免疫组织化学研究。在脾细胞注射后 0.5 天即可识别出明显的血管周围袖口,此后逐渐减少。血管周围的圆形细胞主要由 CD8+T 细胞(65%)和 CD4+T 细胞(10%)组成。血管周围的圆形细胞中 CD3+细胞少于 20%。与 CD8 相比,CD3 的表达减少可能是由于先前的超抗原刺激。这些数据可能与感染性或自身免疫性脑炎的发病机制有关,例如多发性硬化症。