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首页> 外文期刊>The journal of immunology >The Effect of the Amount of Mycobacterial Adjuvants on the Immune Response of Strain 2, Strain 13 and Hartley Strain Guinea Pigs to DNP-PLL and DNP-GL
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The Effect of the Amount of Mycobacterial Adjuvants on the Immune Response of Strain 2, Strain 13 and Hartley Strain Guinea Pigs to DNP-PLL and DNP-GL

机译:分枝杆菌佐剂的量对菌株2、13,Hartley豚鼠对DNP-PLL和DNP-GL免疫反应的影响

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The effect of the concentration of mycobacterial adjuvants on the immune response of strain 2, strain 13 and Hartley guinea pigs to DNP-PLL and DNP-GL was investigated. The ability to respond to these antigens in guinea pigs is controlled by a dominant autosomal gene. A small number of non-responder strain 13 animals or Hartley non-responder animals produced low serum levels of anti-DNP antibodies following prolonged immunization with DNP-PLL and 0.5 mg/ml Mycobacterium butyricum . These antibodies were detected by a modified Farr technique using high specific activity 3H DNP-EACA. However, none of the non-responder guinea pigs similarly immunized with DNP-GL produced detectable antibodies. When the amount of mycobacteria in the adjuvant was increased to 10 mg/ml Mycobacterium tuberculosis , all non-responder animals immunized with DNP-PLL produced measurable concentrations of anti-DNP antibodies late in immunization, but these levels were much lower than those observed in genetic responder animals. Furthermore, strain 13 guinea pigs immunized with DNP-GL and large amounts of mycobacteria failed to produce detectable concentrations of anti-DNP antibodies. All non-responder guinea pigs lacking the PLL gene, immunized with these antigens in adjuvants containing either low or high amounts of mycobacteria, failed to show delayed sensitivity to these antigens. In addition, lymph node cells from these immunized animals were not stimulated in vitro by DNP-PLL. The experimental data suggest that in non-responder guinea pigs the positively charged DNP-PLL molecule behaves as a hapten and that mycobacterial antigens, when present in large amounts, act as an immunologic carrier or “Schlepper” molecule.
机译:研究了分枝杆菌佐剂的浓度对菌株2,菌株13和Hartley豚鼠对DNP-PLL和DNP-GL的免疫反应的影响。豚鼠对这些抗原的反应能力由显性常染色体基因控制。长期用DNP-PLL和0.5 mg / ml丁酸分枝杆菌免疫后,少数无反应的13株动物或Hartley无反应的动物产生了低水平的抗DNP抗体。通过使用高比活性3H DNP-EACA的改良Farr技术检测这些抗体。但是,没有任何一种类似的用DNP-GL免疫的无反应性豚鼠不能产生可检测的抗体。当佐剂中的分枝杆菌数量增加到10 mg / ml结核分枝杆菌时,所有用DNP-PLL免疫的无反应动物在免疫后期都会产生可测量浓度的抗DNP抗体,但这些水平远低于基因反应动物。此外,用DNP-GL和大量分枝杆菌免疫的13只豚鼠不能产生可检测浓度的抗DNP抗体。所有缺少PLL基因的无反应豚鼠,在含有低或大量分枝杆菌的佐剂中用这些抗原免疫后,均未表现出对这些抗原的敏感性延迟。另外,来自这些免疫动物的淋巴结细胞没有被DNP-PLL体外刺激。实验数据表明,在无反应的豚鼠中,带正电荷的DNP-PLL分子表现为半抗原,而分枝杆菌抗原大量存在时则充当免疫载体或“ Schlepper”分子。

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