Wolf Andrea J, Desvignes Ludovic, Linas Beth, Banaiee Niaz, Tamura Toshiki, Takatsu Kiyoshi, Ernst Joel D
Division of Infectious Diseases, Department of Medicine, New York University School of Medicine, New York, NY 10016, USA.
J Exp Med. 2008 Jan 21;205(1):105-15. doi: 10.1084/jem.20071367. Epub 2007 Dec 24.
The onset of the adaptive immune response to Mycobacterium tuberculosis is delayed compared with that of other infections or immunization, and allows the bacterial population in the lungs to expand markedly during the preimmune phase of infection. We used adoptive transfer of M. tuberculosis Ag85B-specific CD4(+) T cells to determine that the delayed adaptive response is caused by a delay in initial activation of CD4(+) T cells, which occurs earliest in the local lung-draining mediastinal lymph node. We also found that initial activation of Ag85B-specific T cells depends on production of antigen by bacteria in the lymph node, despite the presence of 100-fold more bacteria in the lungs. Although dendritic cells have been found to transport M. tuberculosis from the lungs to the local lymph node, airway administration of LPS did not accelerate transport of bacteria to the lymph node and did not accelerate activation of Ag85B-specific T cells. These results indicate that delayed initial activation of CD4(+) T cells in tuberculosis is caused by the presence of the bacteria in a compartment that cannot be mobilized from the lungs to the lymph node, where initial T cell activation occurs.
与其他感染或免疫接种相比,对结核分枝杆菌的适应性免疫反应的启动有所延迟,这使得肺部的细菌群体在感染的免疫前期能够显著扩增。我们通过过继转移结核分枝杆菌Ag85B特异性CD4(+) T细胞来确定,延迟的适应性反应是由CD4(+) T细胞的初始激活延迟所导致的,这种初始激活最早发生在局部引流肺的纵隔淋巴结中。我们还发现,Ag85B特异性T细胞的初始激活依赖于淋巴结中细菌产生的抗原,尽管肺部的细菌数量比淋巴结中的多100倍。虽然已发现树突状细胞可将结核分枝杆菌从肺部转运至局部淋巴结,但经气道给予脂多糖并未加速细菌向淋巴结的转运,也未加速Ag85B特异性T细胞的激活。这些结果表明,结核病中CD4(+) T细胞初始激活延迟是由于细菌存在于一个无法从肺部转运至发生初始T细胞激活的淋巴结的隔室中。