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本文引用的文献

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The cellular source of interleukin-6 during Listeria infection.李斯特菌感染期间白细胞介素-6的细胞来源。
Infect Immun. 1993 Jun;61(6):2626-31. doi: 10.1128/iai.61.6.2626-2631.1993.
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Effector mechanisms involved in cytokine-mediated bacteriostasis of Mycobacterium avium infections in murine macrophages.细胞因子介导的鼠巨噬细胞中鸟分枝杆菌感染抑菌作用的效应机制。
Immunology. 1993 Nov;80(3):352-9.
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Detection of in vivo expression of interleukin-10 using a semi-quantitative polymerase chain reaction method in Schistosoma mansoni infected mice.采用半定量聚合酶链反应法检测曼氏血吸虫感染小鼠体内白细胞介素-10的表达
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Accessory signals in murine cytolytic T cell responses. Dual requirement for IL-1 and IL-6.小鼠细胞毒性T细胞反应中的辅助信号。白细胞介素-1和白细胞介素-6的双重需求。
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Tumor necrosis factor-alpha and interleukin 6 synergistically induce T cell growth.
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Recombinant tumour necrosis factor-alpha decreases whereas recombinant interleukin-6 increases growth of a virulent strain of Mycobacterium avium in human macrophages.重组肿瘤坏死因子-α可降低而重组白细胞介素-6可增加人巨噬细胞中鸟分枝杆菌强毒株的生长。
Immunology. 1990 Sep;71(1):139-41.
8
Stimulation of antibacterial macrophage activities by B-cell stimulatory factor 2 (interleukin-6).B细胞刺激因子2(白细胞介素-6)对巨噬细胞抗菌活性的刺激作用。
Infect Immun. 1990 Jan;58(1):269-71. doi: 10.1128/iai.58.1.269-271.1990.
9
Mycobacterium avium-intracellulare induces interleukin-6 from human monocytes and large granular lymphocytes.鸟分枝杆菌-胞内分枝杆菌可诱导人单核细胞和大颗粒淋巴细胞产生白细胞介素-6。
Blood. 1991 May 15;77(10):2218-24.
10
Role of interleukin 6 for differential responsiveness of naive and memory CD4+ T cells in CD2-mediated activation.白细胞介素6在CD2介导的激活中对初始和记忆性CD4+ T细胞差异反应性的作用。
J Exp Med. 1990 Nov 1;172(5):1419-24. doi: 10.1084/jem.172.5.1419.

白细胞介素-6在小鼠分枝杆菌感染期间诱导保护性T细胞中的作用。

Role of interleukin-6 in the induction of protective T cells during mycobacterial infections in mice.

作者信息

Appelberg R, Castro A G, Pedrosa J, Minóprio P

机构信息

Centro de Citologia Experimental, University of Porto, Portugal.

出版信息

Immunology. 1994 Jul;82(3):361-4.

PMID:7959868
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1414867/
Abstract

Interleukin-6 (IL-6) has been shown to regulate numerous functions of the immune system including the differentiation of T-cell subpopulations. Here we examined the involvement of this cytokine in the in vivo generation of a population of T cells able to protect mice against mycobacterial infections. BALB/c mice were infected intravenously with Mycobacterium avium 2447 and anti-IL-6 monoclonal antibodies were administered intraperitoneally throughout the course of the infection. Control mice were able to control the mycobacterial proliferation 1 month after inoculation, whereas mice whose IL-6 had been blocked showed progressive bacterial growth. To distinguish a role for IL-6 associated to the induction or expression of immunity mediated by T cells, we immunized mice with M. bovis bacillus Calmette-Guérin (BCG) Pasteur and challenged them 2 months later with M. avium. One group of mice received anti-IL-6 during the BCG vaccination and another during the M. avium challenge. When M. avium proliferation was assessed at day 30 of the challenge, it was found that the administration of anti-IL-6 during vaccination reduced the protection afforded by BCG compared to administration of the isotype control antibody. No difference in bacterial proliferation was observed at day 30 of challenge when antibodies were administered during M. avium challenge. Our results show that protective T cells arise during M. avium infections in mice after differentiating in the presence of IL-6.

摘要

白细胞介素-6(IL-6)已被证明可调节免疫系统的多种功能,包括T细胞亚群的分化。在此,我们研究了这种细胞因子在能够保护小鼠抵抗分枝杆菌感染的T细胞群体的体内生成过程中的作用。将BALB/c小鼠静脉注射鸟分枝杆菌2447,并在整个感染过程中腹腔注射抗IL-6单克隆抗体。对照小鼠在接种后1个月能够控制分枝杆菌的增殖,而IL-6被阻断的小鼠则出现细菌的进行性生长。为了区分IL-6在由T细胞介导的免疫诱导或表达中的作用,我们用卡介苗(BCG)巴斯德株免疫小鼠,并在2个月后用鸟分枝杆菌攻击它们。一组小鼠在BCG疫苗接种期间接受抗IL-6,另一组在鸟分枝杆菌攻击期间接受抗IL-6。当在攻击第30天评估鸟分枝杆菌的增殖时,发现与同型对照抗体相比,疫苗接种期间给予抗IL-6降低了BCG提供的保护作用。当在鸟分枝杆菌攻击期间给予抗体时,在攻击第30天未观察到细菌增殖的差异。我们的结果表明,保护性T细胞在小鼠感染鸟分枝杆菌期间,在IL-6存在的情况下分化后产生。