Smith Sherry S, Barnum Scott R
Department of Microbiology, University of Alabama at Birmingham, 845 19th St. S., BBRB/842, Birmingham, AL 35294, USA.
J Leukoc Biol. 2008 Jan;83(1):71-9. doi: 10.1189/jlb.0407263. Epub 2007 Oct 10.
The expression of beta 2-integrins on gammadelta T cells in naïve mice or those with experimental autoimmune encephalomyelitis (EAE) remains poorly characterized. We compared beta 2-integrin expression and cytokine production between gammadelta and alphabeta T cells over the acute course of EAE. We observed that unlike in alphabeta T cells, beta 2-integrin expression on gammadelta T cells increased significantly from baseline, peaked at Day 10, and remained unchanged in the draining lymph nodes or declined in the spleen and CNS by Day 15. In addition, IFN-gamma- and TNF-alpha-producing gammadelta T cells infiltrated the CNS rapidly and produced significantly more of these cytokines than alphabeta T cells throughout the course of EAE. These results suggest unique roles for beta 2-integrins in the trafficking of gammadelta versus alphabeta T cells during EAE and that gammadelta T cells infiltrate the CNS rapidly, producing cytokines, which modulate acute disease.
在未接触过抗原的小鼠或患有实验性自身免疫性脑脊髓炎(EAE)的小鼠中,γδ T细胞上β2整合素的表达情况仍未得到充分表征。我们比较了EAE急性期γδ T细胞和αβ T细胞之间β2整合素的表达及细胞因子产生情况。我们观察到,与αβ T细胞不同,γδ T细胞上β2整合素的表达从基线水平显著增加,在第10天达到峰值,在引流淋巴结中保持不变,而在脾脏和中枢神经系统中到第15天时下降。此外,产生IFN-γ和TNF-α的γδ T细胞迅速浸润中枢神经系统,并且在EAE整个病程中产生的这些细胞因子明显多于αβ T细胞。这些结果表明,在EAE期间,β2整合素在γδ T细胞与αβ T细胞的迁移中发挥独特作用,并且γδ T细胞迅速浸润中枢神经系统,产生调节急性疾病的细胞因子。