体内清除CD11c+细胞会延迟CD4+ T细胞对结核分枝杆菌的反应,并加重感染结果。
In vivo depletion of CD11c+ cells delays the CD4+ T cell response to Mycobacterium tuberculosis and exacerbates the outcome of infection.
作者信息
Tian Tian, Woodworth Joshua, Sköld Markus, Behar Samuel M
机构信息
Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
出版信息
J Immunol. 2005 Sep 1;175(5):3268-72. doi: 10.4049/jimmunol.175.5.3268.
Although dendritic cells (DC) are potent APC that prime T cells against many pathogens, there is no direct evidence that DC are required for immunity to Mycobacterium tuberculosis (Mtb) infection. The requirement for DC to prime the CD4+ T cell response following Mtb infection was investigated using pCD11c-diptheria toxin receptor/GFP transgenic mice, in which DC can be transiently ablated in vivo. We show a critical role for DC in initiation of the CD4+ T cell response to the mycobacterial Ag early secretory Ag of tuberculosis 6. The delay in initiating the Ag-specific T cell response led to impaired control of Mtb replication. Interestingly, DC were not required for the secondary CD4+ T cell response following Mtb infection in peptide-vaccinated mice. Thus, this study shows that DC are essential for the initiation of the adaptive T cell response to the human pathogen Mtb.
尽管树突状细胞(DC)是强大的抗原呈递细胞,可启动T细胞对抗多种病原体,但尚无直接证据表明DC是抵抗结核分枝杆菌(Mtb)感染所必需的。使用pCD11c - 白喉毒素受体/绿色荧光蛋白转基因小鼠研究了Mtb感染后DC启动CD4 + T细胞应答的必要性,在这种小鼠中,DC可在体内被短暂清除。我们发现DC在启动针对结核分枝杆菌Ag早期分泌Ag 6的CD4 + T细胞应答中起关键作用。启动Ag特异性T细胞应答的延迟导致对Mtb复制的控制受损。有趣的是,在肽疫苗接种的小鼠中,Mtb感染后的二次CD4 + T细胞应答并不需要DC。因此,本研究表明DC对于启动针对人类病原体Mtb的适应性T细胞应答至关重要。