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内源性和外源性白细胞介素-12增强经都柏林沙门氏菌口服攻击的小鼠的保护性免疫反应。

Endogenous and exogenous interleukin-12 augment the protective immune response in mice orally challenged with Salmonella dublin.

作者信息

Kincy-Cain T, Clements J D, Bost K L

机构信息

Department of Microbiology and Immunology, Tulane University Medical Center, New Orleans, Louisiana 70112-2699, USA.

出版信息

Infect Immun. 1996 Apr;64(4):1437-40. doi: 10.1128/iai.64.4.1437-1440.1996.

Abstract

Following oral challenge with Salmonella dublin, we observed significant increases in interleukin-12 (IL-12) protein expression in the mesenteric lymph nodes. The importance of this endogenous cytokine production in the immune response against S. dublin was demonstrated by in vivo depletion of IL-12 with an anti-IL-12 monoclonal antibody prior to oral S. dublin challenge. Mice pretreated with anti-IL-12 antibody had increased salmonellosis and reduced survival times compared with mice receiving control antibody. Furthermore, administration of exogenous murine recombinant IL-12 dramatically increased survival times of mice challenged orally with S. dublin. Together, these results demonstrate that endogenous and exogenous IL-12 significantly augment the mucosal immune response against the intracellular pathogen S. dublin.

摘要

用都柏林沙门氏菌进行口服激发后,我们观察到肠系膜淋巴结中白细胞介素-12(IL-12)蛋白表达显著增加。在口服都柏林沙门氏菌激发前,用抗IL-12单克隆抗体在体内清除IL-12,证明了这种内源性细胞因子产生在针对都柏林沙门氏菌的免疫反应中的重要性。与接受对照抗体的小鼠相比,用抗IL-12抗体预处理的小鼠沙门氏菌病增加且存活时间缩短。此外,给予外源性小鼠重组IL-12显著延长了经口服都柏林沙门氏菌激发的小鼠的存活时间。这些结果共同表明,内源性和外源性IL-12显著增强了针对细胞内病原体都柏林沙门氏菌的黏膜免疫反应。

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