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Toward quantitative models of germinal center dynamics.

机译:建立生发中心动力学的定量模型。

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This dissertation uses modeling and simulation in order to better understand the immune response. Numerous in vivo and in vitro studies have elucidated the basic cellular mechanisms that underlie many aspects of immune response dynamics. However, in most cases it is not well understood how these mechanisms fit together. This is particularly true for the germinal center reaction (an important component of the immune response). Although many models of the germinal center have been proposed, most only attempt to explain the average-case, qualitative behavior of the system. This dissertation demonstrates that such a methodology can be misleading and presents a number of contributions toward the development of discrete/stochastic, quantitative models of the germinal center reaction.; The work presented in this dissertation is a fusion of computer science and theoretical immunology. Formulas for estimating response-specific model parameters, algorithms for developing discrete/stochastic simulations, and quantitative constraints are combined to provide a framework for asking precise questions about how well germinal center models can explain experimental observations. This framework is used to highlight significant weaknesses in well-known models of the germinal center reaction. To address these problems, new models are proposed and validated. All of these models are used to make specific predictions that can be tested by in vivo experiments to obtain further validation and drive the development of improved models.
机译:为了更好地理解免疫反应,本文采用建模和仿真的方法。大量的体内体外研究阐明了免疫反应动力学许多方面的基础细胞机制。但是,在大多数情况下,人们对这些机制如何配合还不太了解。对于生发中心反应(免疫反应的重要组成部分)尤其如此。尽管已提出了生发中心的许多模型,但大多数仅尝试解释系统的平均情况,定性行为。本文证明了这种方法可能会产生误导,并为生发中心反应的离散/随机,定量模型的发展做出了许多贡献。本文的工作是计算机科学与理论免疫学的融合。结合了用于估计特定于响应的模型参数的公式,用于开发离散/随机模拟的算法以及定量约束,从而提供了一个框架,用于询问有关生发中心模型如何很好地解释实验观察结果的精确问题。此框架用于突出显示生发中心反应模型中的重大缺陷。为了解决这些问题,提出并验证了新模型。所有这些模型都用于做出可以通过体内实验进行测试的特定预测,从而获得进一步的验证并推动改进模型的开发。

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