Bhatt Kamlesh, Hickman Somia Perdow, Salgame Padmini
Department of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, PA 19140, USA.
J Immunol. 2004 Mar 1;172(5):2748-51. doi: 10.4049/jimmunol.172.5.2748.
In this study, we report a new approach that allows dissection of distinct pathways regulating induction of early adaptive immunity in response to Mycobacterium tuberculosis (Mtb). We used traceable murine dendritic cells (DCs) and macrophage populations to chart their migratory pattern in response to Mtb, and found that only DCs receiving inflammatory stimuli from Mtb up-regulated their expression of CCR7 and migrated specifically to the draining lymph nodes (LNs). Furthermore, these Mtb-modulated DCs initiated a Th1 response only in the draining LNs. Taken together, these results demonstrate that Mtb-induced modulation of DCs is critical for their migration to regional LNs and ensuing T cell priming.
在本研究中,我们报告了一种新方法,该方法能够剖析在应对结核分枝杆菌(Mtb)时调节早期适应性免疫诱导的不同途径。我们使用可追踪的小鼠树突状细胞(DCs)和巨噬细胞群体来描绘它们对Mtb的迁移模式,发现只有从Mtb接收炎症刺激的DCs上调其CCR7的表达并特异性迁移至引流淋巴结(LNs)。此外,这些受Mtb调节的DCs仅在引流LNs中引发Th1反应。综上所述,这些结果表明Mtb诱导的DCs调节对于其向局部LNs的迁移以及随后的T细胞启动至关重要。