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白细胞介素-2对免疫反应调节的作用。

The effects of interleukin-2 on immune response regulation.

作者信息

Waters Ryan S, Perry Justin S A, Han SunPil, Bielekova Bibiana, Gedeon Tomas

机构信息

Department of Mathematical Sciences, Montana State University, Bozeman, MT, MT.

Neuroimmunological Diseases Unit, National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health (NIH), Bethesda, MD.

出版信息

Math Med Biol. 2018 Mar 14;35(1):79-119. doi: 10.1093/imammb/dqw021.

Abstract

The immune system has many adaptive and dynamic components that are regulated to ensure appropriate, precise and rapid response to a foreign pathogen. A delayed or inadequate immune response can lead to prolonged disease, while an excessive or under-regulated response can lead to autoimmunity. The cytokine, interleukin-2 (IL-2) and its receptor IL-2R play an important role in maintaining this balance.The IL-2 receptor transduces pSTAT5 signal through both the intermediate and high affinity receptors, which differ from each other by the presence of CD25 chain in IL-2 receptor. We present experimental data on the kinetics of pSTAT5 signalling through both of the receptors and develop a model that captures this kinetics. We then use this model to parameterize key aspects of two additional models in which we propose and study two different mechanisms by which IL-2 receptor can transduce distinct signals leading to either an activated or a non-activated cell state. We speculate that this initial state differentiation, perhaps enhanced by downstream feedbacks, may eventually lead to differential cell fates.Our result shows that non-linear dynamical models can suggest resolution of a puzzling array of seemingly contradictory experimental results on IL-2 effect on proliferation and differentiation of T-cells.

摘要

免疫系统有许多适应性和动态性的组成部分,这些部分受到调节以确保对外来病原体做出适当、精确和快速的反应。免疫反应延迟或不足会导致疾病迁延不愈,而反应过度或调节不当则会导致自身免疫。细胞因子白细胞介素-2(IL-2)及其受体IL-2R在维持这种平衡中发挥着重要作用。IL-2受体通过中亲和性和高亲和性受体转导pSTAT5信号,这两种受体的区别在于IL-2受体中是否存在CD25链。我们展示了通过这两种受体的pSTAT5信号传导动力学的实验数据,并建立了一个捕捉这种动力学的模型。然后,我们使用这个模型对另外两个模型的关键方面进行参数化,在这两个模型中,我们提出并研究了IL-2受体转导导致细胞处于激活或未激活状态的不同信号的两种不同机制。我们推测,这种初始状态的分化,可能会因下游反馈而增强,最终可能导致不同的细胞命运。我们的结果表明,非线性动力学模型可以解释一系列关于IL-2对T细胞增殖和分化影响的看似矛盾的实验结果。

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