Cardell S, Sander B, Möller G
Department of Immunology, Arrhenius Laboratories for Natural Sciences, Stockholm University, Sweden.
Scand J Immunol. 1992 Dec;36(6):769-77. doi: 10.1111/j.1365-3083.1992.tb03138.x.
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.
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。