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Mycobacterium leprae alters classical activation of human monocytes in vitro

机译:麻风分枝杆菌在体外改变人类单核细胞的经典激活

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BackgroundMacrophages play a central role in the pathogenesis of leprosy, caused by Mycobacterium leprae. The polarized clinical presentations in leprosy are associated with differential immune activation. In tuberculoid leprosy, macrophages show a classical activation phenotype (M1), while macrophages in lepromatous disease display characteristics of alternative activation (M2). Bacille Calmette-Guérin (BCG) vaccination, which protects against leprosy, can promote sustained changes in monocyte response to unrelated pathogens and may preferentially direct monocytes towards an M1 protective phenotype. We previously reported that M. leprae can dampen the response of naïve human monocytes to a strong inducer of pro-inflammatory cytokines, such as BCG. Here, we investigated the ability of the pathogen to alter the direction of macrophage polarization and the impact of BCG vaccination on the monocyte response to M. leprae.
机译:背景巨噬细胞在麻风分枝杆菌引起的麻风病发病机理中起着核心作用。麻风病的极化临床表现与差异免疫激活有关。在结核性麻风病中,巨噬细胞显示出经典的激活表型(M1),而在麻风病中巨噬细胞则显示出替代激活(M2)的特征。 BacilleCalmette-Guérin(BCG)疫苗可预防麻风病,可促进单核细胞对无关病原体的持续变化,并可优先引导单核细胞趋向于M1保护表型。我们以前曾报道过,麻风分枝杆菌可以抑制幼稚的人类单核细胞对促炎性细胞因子(如BCG)的强诱导剂的反应。在这里,我们调查了病原体改变巨噬细胞极化方向的能力以及卡介苗接种对麻风单胞菌的单核细胞反应的影响。

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