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巨噬细胞和淋巴细胞在抵抗嗜肺军团菌感染中的不同作用。

Differing macrophage and lymphocyte roles in resistance to Legionella pneumophila infection.

作者信息

Yamamoto Y, Klein T W, Newton C, Friedman H

机构信息

Department of Medical Microbiology and Immunology, University of South Florida College of Medicine, Tampa 33612.

出版信息

J Immunol. 1992 Jan 15;148(2):584-9.

PMID:1729375
Abstract

Similar to guinea pig macrophages and human monocytes, macrophages from the peritoneal cavity of thioglycolate pretreated A/J mice are permissive for growth of Legionella pneumophila. In contrast, macrophages from BDF1 mice are not permissive for L. pneumophila. Lymphocytes from A/J and BDF1 mice proliferated in response to Legionella Ag but guinea pig lymphocytes did not. Also, splenocyte cultures from A/J mice treated with either Con A or Legionella vaccine produced supernatants which induced A/J macrophages to restrict Legionella growth, but guinea pig splenocyte culture supernatants obtained after stimulation with L. pneumophila vaccine did not induce Legionella growth restriction activity by guinea pig macrophages. Murine rIFN-gamma but not rIFN-alpha markedly inhibited growth of Legionella in A/J mouse macrophages and monoclonal anti-IFN-gamma antibody neutralized the anti-Legionella activity of culture supernatants from A/J mouse splenocytes responding to Legionella Ag. From these data, IFN-gamma appears to be an important factor in anti-Legionella activity of Ag-activated mouse splenocyte culture supernatants. Cyclosporin A, when given to either A/J or BDF1 mice, reduced the proliferation responses of splenocytes to T cell mitogens and also decreased the IFN production of A/J spleen cells to Legionella Ag. In addition, drug treatment decreased the resistance of A/J mice to Legionella infection as shown by an increase in the number of viable bacteria in the liver. However, injection of drug treated mice with lymphokine-rich splenocyte culture supernatant reconstituted the resistance of these animals. These results suggest an important role for lymphocyte activation and lymphokine production in the resistance of A/J mice to Legionella infection. The greater resistance of BDF1 mice, however, may result from nonpermissive macrophages and responsive lymphocytes. In the case of guinea pigs, susceptibility to Legionella infections may result from both the permissive nature of the macrophages and the relatively unresponsive nature of the lymphocytes in these animals.

摘要

与豚鼠巨噬细胞和人类单核细胞相似,硫乙醇酸盐预处理的A/J小鼠腹腔巨噬细胞可允许嗜肺军团菌生长。相比之下,BDF1小鼠的巨噬细胞不允许嗜肺军团菌生长。A/J和BDF1小鼠的淋巴细胞对军团菌抗原产生增殖反应,但豚鼠淋巴细胞则无此反应。此外,用刀豆蛋白A或军团菌疫苗处理的A/J小鼠脾细胞培养物产生的上清液可诱导A/J巨噬细胞限制军团菌生长,但用嗜肺军团菌疫苗刺激后获得的豚鼠脾细胞培养上清液不能诱导豚鼠巨噬细胞产生军团菌生长限制活性。小鼠重组干扰素-γ而非重组干扰素-α可显著抑制嗜肺军团菌在A/J小鼠巨噬细胞中的生长,单克隆抗干扰素-γ抗体可中和A/J小鼠脾细胞对军团菌抗原反应的培养上清液的抗军团菌活性。根据这些数据,干扰素-γ似乎是抗原激活的小鼠脾细胞培养上清液抗军团菌活性的重要因素。当给A/J或BDF1小鼠注射环孢素A时,可降低脾细胞对T细胞有丝分裂原的增殖反应,并减少A/J脾细胞对军团菌抗原的干扰素产生。此外,药物处理降低了A/J小鼠对军团菌感染的抵抗力,表现为肝脏中活菌数量增加。然而,给药物处理的小鼠注射富含淋巴因子的脾细胞培养上清液可恢复这些动物的抵抗力。这些结果表明淋巴细胞激活和淋巴因子产生在A/J小鼠抵抗军团菌感染中起重要作用。然而,BDF1小鼠更强的抵抗力可能源于不允许生长的巨噬细胞和有反应的淋巴细胞。就豚鼠而言,对军团菌感染的易感性可能源于这些动物巨噬细胞的允许生长特性和淋巴细胞相对无反应的特性。

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