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Dynamics of Immunological Models

机译:免疫模型动力学

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We analyse the effect of the regulatory T cells (Tregs) in the local control of the immune responses by T cells. We obtain an explicit formula for the level of antigenic stimulation of T cells as a function of the concentration of T cells and the parameters of the model. The relation between the concentration of the T cells and the antigenic stimulation of T cells is an hysteresis, that is unfold for some parameter values. We study the appearance of autoimmunity from cross-reactivity between a pathogen and a self antigen or from bystander proliferation. We also study an asymmetry in the death rates. With this asymmetry we show that the antigenic stimulation of the Tregs is able to control locally the population size of Tregs. Other effects of this asymmetry are a faster immune response and an improvement in the simulations of the bystander proliferation. The rate of variation of the levels of antigenic stimulation determines if the outcome is an immune response or if Tregs are able to maintain control due to the presence of a transcritical bifurcation for some tuning between the antigenic stimuli of T cells and Tregs. This behavior is explained by the presence of a transcritical bifurcation.
机译:我们分析了调节性T细胞(Tregs)在由T细胞对免疫反应的局部控制中的作用。我们获得了针对T细胞的抗原刺激水平作为T细胞浓度和模型参数的函数的明确公式。 T细胞的浓度与T细胞的抗原刺激之间的关系是一个滞后现象,对于某些参数值而言,这是展开的。我们研究了由病原体和自身抗原之间的交叉反应或旁观者增殖引起的自身免疫的出现。我们还研究了死亡率的不对称性。通过这种不对称,我们表明抗原调节性Treg能够刺激局部调节Tregs的大小。这种不对称的其他影响是更快的免疫反应和旁观者扩散模拟的改善。抗原刺激水平的变化率决定结果是免疫应答还是由于跨临界分叉的存在,Treg是否能够维持控制,从而在T细胞和Treg的抗原刺激之间进行某种调节。通过跨临界分叉的存在来解释此行为。

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