首页> 外文期刊>Immunology and Cell Biology >Vaccination of brushtail possums, Trichosurus vulpecula, with Bacille Calmette-Guerin induces T lymphocytes that reduce Mycobacterium bovis replication in alveolar macrophages via a contact-dependentitric oxide-independent mechanism.
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Vaccination of brushtail possums, Trichosurus vulpecula, with Bacille Calmette-Guerin induces T lymphocytes that reduce Mycobacterium bovis replication in alveolar macrophages via a contact-dependentitric oxide-independent mechanism.

机译:用芽孢杆菌(Bacille Calmette-Guerin)接种猪尾负鼠Trichosurus vulpecula诱导T淋巴细胞,该T淋巴细胞通过接触依赖性/一氧化氮非依赖性机制减少了肺泡巨噬细胞中牛分枝杆菌的复制。

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The permissiveness of alveolar macrophages from brushtail possums for the replication of Mycobacterium bovis was examined. Mycobacterium bovis replication was indirectly measured by assessing bacterial metabolism via the incorporation of [3-H]-uracil by bacilli released from lysed macrophages previously infected with mycobacteria. Alveolar macrophages allowed substantial replication of virulent M. bovis, in contrast to Bacille Calmette-Guerin (BCG) Pasteur, which replicated poorly. The addition of crude lymphokines enhanced the metabolic activity of phagocytosed M. bovis in possum macrophages. Possum lymphokines enhanced the ability of possum macrophages to generate reactive oxygen intermediates, measured by the reduction of nitroblue tetrazolium, which is indicative of an activation process. Similarly, the addition of recombinant possum TNF-alpha enhanced the permissiveness of alveolar macrophages for M. bovis. In contrast to mouse peritoneal macrophages, possum alveolar macrophages did not release significant levels of nitric oxide (NO) after stimulation with M. bovis and/or lymphokines. However, the uptake of virulent M. bovis by possum macrophages was associated with an enhanced ability of cells to release TNF-alpha, whereas very low levels of TNF-alpha were released after infection with BCG. The addition of a selective inhibitor of inducible NO synthase had no impact on the replication of M. bovis or BCG in possum macrophages in the presence or absence of lymphokines. Co-culturing infected possum alveolar macrophages with autologous blood mononuclear cells from BCG-vaccinated possums led to a significant decrease in the metabolic activity of intracellular M. bovis. This effect was contact dependent and NO independent and was mediated by a population of CD3+ cells. In addition, adding scavengers of reactive oxygen intermediates did not abrogate this phenomenon.
机译:检查了牛尾负鼠肺泡巨噬细胞对牛分枝杆菌复制的允许性。牛分枝杆菌的复制是通过评估细菌的代谢而间接测量的,该细菌的代谢是由先前感染过分枝杆菌的裂解巨噬细胞释放的细菌掺入[3-H]-尿嘧啶来进行的。与Bacille Calmette-Guerin(BCG)巴斯德菌复制能力差的情况相比,肺泡巨噬细胞可大量复制有毒的牛分枝杆菌。粗淋巴因子的添加增强了负鼠巨噬细胞中吞噬的牛分枝杆菌的代谢活性。负鼠淋巴因子增强了负鼠巨噬细胞产生活性氧中间体的能力,这是通过还原硝基蓝四唑鎓来衡量的,这表明了活化过程。同样,重组负鼠TNF-α的添加增强了肺泡巨噬细胞对牛分枝杆菌的容忍度。与小鼠腹膜巨噬细胞相反,负鼠肺泡巨噬细胞和/或淋巴因子刺激后负鼠肺泡巨噬细胞未释放明显水平的一氧化氮(NO)。然而,负鼠巨噬细胞对有毒牛分枝杆菌的吸收与细胞释放TNF-α的能力增强有关,而卡介苗感染后却释放出极低水平的TNF-α。在存在或不存在淋巴因子的情况下,添加诱导型NO合酶的选择性抑制剂对负鼠巨噬细胞中牛分枝杆菌或BCG的复制没有影响。将感染的负鼠肺泡巨噬细胞与BCG接种负鼠的自体血液单核细胞共培养会导致细胞内牛分枝杆菌的代谢活性显着下降。这种作用是接触依赖性和NO依赖性的,并由一群CD3 +细胞介导。另外,添加活性氧中间体的清除剂不能消除该现象。

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