抗原表位筛选与免疫应答中的细胞协同作用

F. Castiglione, M. Bernaschi
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引用次数: 2

摘要

我们提出了系统生物学和免疫信息学技术的组合来模拟免疫反应。代表分子结合位点的氨基酸序列和基于生物信息学的T和B细胞表位预测成为基于代理的模拟器的组成部分。为了确定入侵抗原的免疫原性部分,我们采用现有的预测方法,并使用Miyazawa和Jernigan蛋白-蛋白电位测量方法来评估分子结合。用经典的免疫实验作为模型的基准。我们还通过淋巴细胞在慢性暴露于免疫原性分子的情况下出现一个或多个主导克隆来再现亲和成熟现象。这些结果表明,模拟器产生的动力学是稳定的,符合基本的免疫学知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epitope Screening and Cell Cooperation in the Immune Response
We present a combination of techniques of systems biology and immunoinformatics to simulate the immune response. Amino acid sequences representing molecular binding sites and bioinformatics based predictions of T and B cell epitopes become components of an agent-based simulator. To determine the immunogenic parts of the invading antigen, we resort to existing prediction methods together with a method, which uses Miyazawa and Jernigan protein–protein potential measurements, for assessing molecular binding. A classical immunization experiment is used as benchmark of the resulting model. We also reproduce the affinity maturation phenomena by the emergence of one or more dominating clones of lymphocytes in the situation of chronic exposure to the immunogenic molecule. These results show that the simulator produces a dynamics that is stable and consistent with basic immunological knowledge.
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