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Pneumocystis carinii infection in young non-immunosuppressed rabbits. Kinetics of infection and of the primary specific immune response.

机译:在未免疫抑制的幼兔中卡氏肺孢子虫感染。感染动力学和主要的特异性免疫反应。

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The aim of this study was to determine the kinetics, the dissemination of the infection and the immunological response to Pneumocystis carinii primary infection in a non-immunosuppressed rabbit model. For this purpose, we developed a nested PCR that amplified a portion of the mitochondrial large-subunit rRNA gene of rabbit-derived P. carinii. The PCR detected P. carinii DNA in lung and bronchoalveolar lavage fluids from 14- to 45-day-old rabbits but not in their serum. No P. carinii DNA was detected in extrapulmonary organs from 28-day-old rabbits with P. carinii pneumonia. ELISA and immunoblotting analysis showed that 5-day-old pups had elevated specific IgG. The IgG concentration sharply decreased, reaching a trough on day 21, and from then onwards progressively increased as the infection cleared. Conversely, the specific IgM concentration increased during the infection and peaked on day 28. IgG mainly recognized a 50-kDa subunit of P. carinii organisms; IgM recognized first a 45-kDa subunit on day 21, whereas from day 28 onwards it also recognized the 50-kDa subunit. A P. carinii-specific splenocyte proliferative response was observed on day 45. These findings suggest that P. carinii primary infection is a time-limited and a lung-limited event and contribute new information on the relationship between the kinetics of primary P. carinii infection and the immunological response in a model that mimics the primary infections in humans.
机译:这项研究的目的是在非免疫抑制的兔模型中确定动力学,感染的传播和对卡氏肺孢子虫原发感染的免疫反应。为此,我们开发了一种巢式PCR,可扩增兔衍生的卡氏疟原虫的线粒体大亚基rRNA基因的一部分。 PCR检测到14至45天大的兔子的肺和支气管肺泡灌洗液中的卡氏疟原虫DNA,但血清中却没有。在28日龄患有卡氏假单胞菌肺炎的兔子的肺外器官中未检测到卡氏假单胞菌DNA。 ELISA和免疫印迹分析表明,5天大的幼犬的特异性IgG升高。 IgG浓度急剧下降,在第21天达到谷底,此后随着感染清除而逐渐增加。相反,特异性IgM浓度在感染过程中增加,并在第28天达到峰值。IgG主要识别卡氏疟原虫生物体的50 kDa亚基。 IgM在第21天首先识别出一个45 kDa的亚基,而从第28天起,它也识别出了50 kDa的亚基。在第45天观察到了卡氏疟原虫特异的脾细胞增殖反应。这些发现表明卡氏疟原虫原发性感染是有时间限制和肺部受限的事件,为原发卡氏疟原虫动力学之间的关系提供了新信息。模拟人类原发感染的模型中的感染和免疫反应。

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