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从经百日咳博德特氏菌气溶胶感染的小鼠的气管支气管淋巴结和脾脏分离出的淋巴细胞的增殖反应、γ干扰素和肿瘤坏死因子的产生。

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.

作者信息

Petersen J W, Ibsen P H, Hasløv K, Heron I

机构信息

Bacterial Vaccine Department Statens Seruminstitut, Copenhagen, Denmark.

出版信息

Infect Immun. 1992 Nov;60(11):4563-70. doi: 10.1128/iai.60.11.4563-4570.1992.

Abstract

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.

摘要

一组小鼠通过气溶胶感染了活的、有毒力的百日咳博德特氏菌。在感染后的7周内,每隔1周从小鼠的气管支气管淋巴结(TBL)和脾脏(SPL)中分离淋巴细胞。测量分离出的淋巴细胞在全灭活百日咳博德特氏菌刺激下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,作为细胞介导免疫(CMI)的参数。通过计算小鼠肺部的CFU来监测感染过程。此外,评估血清中针对一系列百日咳博德特氏菌抗原的抗体反应。结果表明,感染诱导了TBL和SPL对全灭活百日咳博德特氏菌刺激的强烈增殖反应。TBL的增殖反应明显高于SPL的反应。增殖反应在感染后3至4周达到最大值,并且在特异性刺激下体外γ干扰素和肿瘤坏死因子的产生与之平行。观察到CMI的发展与肺部感染的清除同时发生。只有在感染清除后,血清中的抗体反应才变得可测量。在感染后3周,在小鼠中成功证明了针对百日咳毒素、丝状血凝素、69 kDa外膜蛋白以及凝集原2和3的特异性CMI,这些抗原正在考虑纳入未来的无细胞百日咳疫苗中。

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