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首页> 外文期刊>Infection and immunity >Proliferative responses and gamma interferon and tumor necrosis factor production by lymphocytes isolated from tracheobroncheal lymph nodes and spleen of mice aerosol infected with Bordetella pertussis.
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Proliferative responses and gamma interferon and tumor necrosis factor production by lymphocytes isolated from tracheobroncheal lymph nodes and spleen of mice aerosol infected with Bordetella pertussis.

机译:百日咳博德特氏菌感染小鼠气管支气管淋巴结和脾脏分离的淋巴细胞产生的增殖反应以及γ干扰素和肿瘤坏死因子的产生。

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A group of mice was aerosol infected with live, virulent Bordetella pertussis bacteria. During a period of 7 weeks following the infection, with intervals of 1 week, lymphocytes were isolated from the tracheobroncheal lymph nodes (TBL) and the spleens (SPL) of the infected mice. The in vitro proliferative responses as well as the gamma interferon and tumor necrosis factor production levels of the isolated lymphocytes in response to stimulation with whole killed B. pertussis bacteria were measured as parameters for cell-mediated immunity (CMI). The course of the infection was monitored by counting of CFU in the lungs of the mice. Moreover, antibody responses in serum against a range of B. pertussis antigens were assessed. The results showed that a vigorous proliferative response of the TBL and SPL to stimulation with whole killed B. pertussis bacteria was induced by the infection. The proliferative response of the TBL was significantly higher than the response of the SPL. The proliferative responses were maximal 3 to 4 weeks after the infection and were paralleled by in vitro gamma interferon and tumor necrosis factor production upon specific stimulation. The development of the CMI was observed simultaneously with the clearance of the infection from the lungs. Antibody responses became measurable in the sera only after the infection was cleared. A specific CMI against pertussis toxin, the filamentous hemagglutinin, the 69-kDa outer membrane protein, and the agglutinogens 2 and 3, antigens which are under consideration for inclusion in future acellular pertussis vaccines, was successfully demonstrated in mice 3 weeks after the infection.
机译:一组小鼠被活的,剧毒的百日咳博德特氏菌气溶胶感染。在感染后的7周内,以1周为间隔,从感染小鼠的气管支气管淋巴结(TBL)和脾脏(SPL)中分离出淋巴细胞。测量了被完全杀死的百日咳博德特氏菌刺激后的离体淋巴细胞的体外增殖反应以及γ干扰素和肿瘤坏死因子的产生水平,作为细胞介导的免疫(CMI)的参数。通过计数小鼠肺中的CFU来监测感染过程。此外,评估了血清中针对百日咳博德特氏菌抗原的抗体反应。结果表明,感染引起了TBL和SPL对被完全杀死的百日咳博德特氏菌的刺激的强烈增殖反应。 TBL的增殖反应显着高于SPL的反应。感染后3至4周,增殖反应最大,并在特定刺激下与体外γ干扰素和肿瘤坏死因子产生平行。在清除肺部感染的同时观察到CMI的发展。仅在清除感染后,抗体反应才能在血清中测量。在感染后三周,已成功在小鼠中证明了一种针对百日咳毒素,丝状血凝素,69 kDa外膜蛋白以及凝集素原2和3的特异性CMI,这些抗原正在考虑纳入未来的脱细胞百日咳疫苗中。

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