Vankayalapati R, Wizel B, Weis S E, Samten B, Girard W M, Barnes P F
Center for Pulmonary and Infectious Disease Control, University of Texas Health Center, Tyler, TX 75708-3154, USA.
J Infect Dis. 2000 Jul;182(1):234-9. doi: 10.1086/315656. Epub 2000 Jun 29.
To investigate the role of interleukin (IL)-18 in human tuberculosis, IL-18 production was evaluated in blood and at the site of disease in patients with tuberculosis. Mycobacterium tuberculosis-stimulated peripheral blood mononuclear cells (PBMC) from tuberculosis patients secreted less IL-18 and interferon-gamma (IFN-gamma) than did PBMC from healthy persons reactive to tuberculin. M. tuberculosis-induced IFN-gamma production was inhibited by anti-IL-18 and enhanced by recombinant IL-18. Alveolar macrophages secreted IL-18 in response to M. tuberculosis, and IL-18 and IFN-gamma concentrations were higher in pleural fluid of patients with tuberculosis than in pleural fluid of patients with nontuberculous diseases. These findings demonstrate that IL-18 production by PBMC correlates with IFN-gamma production and effective immunity to tuberculosis, suggesting that IL-18 contributes to a protective type 1 cytokine response in persons with mycobacterial infection.
为研究白细胞介素(IL)-18在人类结核病中的作用,对结核病患者血液及病灶部位的IL-18生成情况进行了评估。结核分枝杆菌刺激的结核病患者外周血单个核细胞(PBMC)分泌的IL-18和干扰素-γ(IFN-γ)比结核菌素反应阳性健康人的PBMC分泌的少。抗IL-18可抑制结核分枝杆菌诱导的IFN-γ生成,而重组IL-18则可增强该生成。肺泡巨噬细胞对结核分枝杆菌产生反应分泌IL-18,结核病患者胸腔积液中的IL-18和IFN-γ浓度高于非结核性疾病患者的胸腔积液。这些发现表明,PBMC产生的IL-18与IFN-γ生成及对结核病的有效免疫相关,提示IL-18有助于分枝杆菌感染患者产生保护性1型细胞因子反应。