Hsu Nai-Jen, Francisco Ngiambudulu M, Keeton Roanne, Allie Nasiema, Quesniaux Valérie F J, Ryffel Bernhard, Jacobs Muazzam
Division of Immunology, Department of Pathology, Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town , Cape Town , South Africa.
CNRS UMR7355, Experimental and Molecular Immunology and Neurogenetics , Orleans , France.
Front Immunol. 2017 Feb 23;8:180. doi: 10.3389/fimmu.2017.00180. eCollection 2017.
Tuberculosis of the central nervous system (CNS-TB) is a devastating complication of tuberculosis, and tumor necrosis factor (TNF) is crucial for innate immunity and controlling the infection. TNF is produced by many cell types upon activation, in particularly the myeloid and T cells during neuroinflammation. Here we used mice with TNF ablation targeted to myeloid and T cell (MT-TNF) to assess the contribution of myeloid and T cell-derived TNF in immune responses during CNS-TB. These mice exhibited impaired innate immunity and high susceptibility to cerebral infection, a similar phenotype to complete TNF-deficient mice. Further, MT-TNF mice were not able to control T cell responses and cytokine/chemokine production. Thus, our data suggested that collective TNF production by both myeloid and T cells are required to provide overall protective immunity against CNS-TB infection.
中枢神经系统结核病(CNS-TB)是结核病的一种毁灭性并发症,肿瘤坏死因子(TNF)对于先天免疫和控制感染至关重要。TNF在激活后由多种细胞类型产生,特别是在神经炎症期间由髓系细胞和T细胞产生。在这里,我们使用了髓系和T细胞靶向TNF缺失的小鼠(MT-TNF)来评估髓系和T细胞来源的TNF在CNS-TB免疫反应中的作用。这些小鼠表现出先天免疫受损和对脑感染的高度易感性,这与完全缺乏TNF的小鼠的表型相似。此外,MT-TNF小鼠无法控制T细胞反应以及细胞因子/趋化因子的产生。因此,我们的数据表明,髓系细胞和T细胞共同产生TNF对于提供针对CNS-TB感染的全面保护性免疫是必需的。