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Mycobacterium indicus pranii (MIP) mediated host protective intracellular mechanisms against tuberculosis infection: Involvement of TLR-4 mediated signaling

机译:分枝杆菌(MIP)介导的宿主保护细胞内抗结核感染细胞内机制:TLR-4介导的信号传导的参与

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Mycobacterium tuberculosis infection inflicts the disease Tuberculosis (TB), which is fatal if left untreated. During M. tuberculosis infection, the pathogen modulates TLR-4 receptor down-stream signaling, indicating the possible involvement of TLR-4 in the regulation of the host immune response. Mycobacterium indicus pranii (MIP) possesses immuno-modulatory properties which induces the pro-inflammatory responses via induction of TLR-4-mediated signaling. Here, we observed the immunomodulatory properties of MIP against tuberculosis infection. We have studied the detailed signaling mechanisms employed by MIP in order to restore-the host immune response against the in vitro tuberculosis infection. We observed that in infected macrophages MIP treatment significantly increased the TLR-4 expression as well as activation of its downstream signaling, facilitating the activation of P38 MAP kinase. MIP treatment was able to activate NF-kappa B via involvement of TLR-4 signaling leading to the enhanced pro inflammatory cytokine and NO generation in the infected macrophages and generation of protective immune response. Therefore, we may suggest that, TLR4 may represent a novel therapeutic target for the activation of the innate immune response during Tuberculosis infection. (C) 2016 Published by Elsevier Ltd.
机译:结核分枝杆菌感染造成疾病结核病(TB),如果没有治疗,这是致命的。在结核病感染期间,病原体调节TLR-4受体下流信号传导,表明TLR-4在宿主免疫应答的调节中可能涉及。 Cocobacterium Quanium(MIP)具有免疫调节性质,其通过诱导TLR-4介导的信号传导诱导促炎反应。在这里,我们观察到MIP对结核感染的免疫调节性质。我们研究了MIP采用的详细信号传导机制,以恢复对体外结核感染的宿主免疫应答。我们观察到,在感染的巨噬细胞MIP处理中,TLR-4表达显着增加了其下游信号的激活,促进了P38 MAP激酶的激活。 MIP处理能够通过TLR-4信号传导的参与激活NF-Kappa B,导致增强的促炎细胞因子,并且在感染的巨噬细胞中没有发电以及保护免疫反应的产生。因此,我们可能表明,TLR4可以代表在结核病感染期间激活先天免疫应答的新型治疗靶标。 (c)2016由elestvier有限公司出版

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