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在白细胞介素-4或γ干扰素存在的情况下对CD4+细胞进行初次刺激,会改变再次刺激时产生细胞因子的细胞频率。

Primary stimulation of CD4+ cells in the presence of IL-4 or IFN-gamma alters the frequencies of cytokine-producing cells at restimulation.

作者信息

Cardell S, Sander B, Möller G

机构信息

Department of Immunology, Arrhenius Laboratories for Natural Sciences, Stockholm University, Sweden.

出版信息

Scand J Immunol. 1992 Dec;36(6):769-77. doi: 10.1111/j.1365-3083.1992.tb03138.x.

DOI:10.1111/j.1365-3083.1992.tb03138.x
PMID:1361075
Abstract

The induction of specific effector functions in naive T cells may be directed by accessory signals during activation. These could be elicited through binding to cell surface molecules or through factors secreted by antigen-presenting cells or other simultaneously activated cells. We have investigated the influence of CD8+ cells and of exogenously added cytokines (interleukin (IL)-2, IL-4 and interferon (IFN)-gamma) on the cytokine production in splenic CD4+ T cells. IL-2, IL-4, IL-5 and IFN-gamma production in CD4+ cells was measured at the single cell level during primary mitogen stimulation in vitro in the presence or absence of factors or CD8+ cells. On day 5 the cells were restimulated with mitogen alone and analysed to evaluate the short-term development of cytokine-producing cells in such cultures. Preactivation in the presence of either exogenous IL-4 or IFN-gamma led to an increased production of IL-4 and IFN-gamma respectively at restimulation, and the effects of both IL-4 and IFN-gamma were augmented by IL-2. After preactivation in the presence of IL-2 and IL-4, every third CD4+ cell could be induced to produce IL-4. Exogenous IL-4 or IFN-gamma further decreased each other's production. Depletion of CD8+ cells before activation resulted in a slight increase of IL-4-producing cells, indicating that simultaneous activation of CD8+ cells will influence lymphokine production in CD4+ cells. The results suggest that the pattern of lymphokines induced in naive cells may be influenced by factors secreted by preactivated CD4+ and CD8+ cells, and that naive cells are preferentially 'recruited' to produce similar cytokines.

摘要

在初始T细胞中,特定效应功能的诱导可能在激活过程中由辅助信号引导。这些信号可以通过与细胞表面分子结合或通过抗原呈递细胞或其他同时被激活的细胞分泌的因子引发。我们研究了CD8 +细胞和外源性添加的细胞因子(白细胞介素(IL)-2、IL-4和干扰素(IFN)-γ)对脾CD4 + T细胞中细胞因子产生的影响。在体外原代有丝分裂原刺激期间,在存在或不存在因子或CD8 +细胞的情况下,在单细胞水平上测量CD4 +细胞中IL-2、IL-4、IL-5和IFN-γ的产生。在第5天,用单独的有丝分裂原再次刺激细胞,并进行分析以评估此类培养物中产生细胞因子的细胞的短期发育情况。在存在外源性IL-4或IFN-γ的情况下进行预激活分别导致再次刺激时IL-4和IFN-γ的产生增加,并且IL-2增强了IL-4和IFN-γ的作用。在存在IL-2和IL-4的情况下进行预激活后,每三个CD4 +细胞中就有一个可以被诱导产生IL-4。外源性IL-4或IFN-γ进一步降低了彼此的产生。激活前耗尽CD8 +细胞导致产生IL-4的细胞略有增加,这表明CD8 +细胞的同时激活会影响CD4 +细胞中淋巴因子的产生。结果表明,初始细胞中诱导的淋巴因子模式可能受预激活的CD4 +和CD8 +细胞分泌的因子影响,并且初始细胞优先被“招募”以产生相似的细胞因子。

相似文献

1
Primary stimulation of CD4+ cells in the presence of IL-4 or IFN-gamma alters the frequencies of cytokine-producing cells at restimulation.在白细胞介素-4或γ干扰素存在的情况下对CD4+细胞进行初次刺激,会改变再次刺激时产生细胞因子的细胞频率。
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Qualitative shift of lymphokine production in response to stimulation, as a consequence of preactivation in vivo or in vitro.由于体内或体外预激活,淋巴细胞因子产生对刺激的反应发生定性转变。
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引用本文的文献

1
Induction of interleukin 4 (IL-4) expression in T helper (Th) cells is not dependent on IL-4 from non-Th cells.辅助性T细胞(Th)中白细胞介素4(IL-4)表达的诱导不依赖于非Th细胞产生的IL-4。
J Exp Med. 1994 Apr 1;179(4):1349-53. doi: 10.1084/jem.179.4.1349.
2
IgE antibody production is associated with suppressed interferon-gamma levels in mesenteric lymph nodes of rats infected with the nematode Nippostrongylus brasiliensis.在感染巴西日圆线虫的大鼠肠系膜淋巴结中,IgE抗体产生与干扰素-γ水平受抑制有关。
Immunology. 1994 Jul;82(3):427-32.