An artificial t cell immune system for predicting MHC-II binding peptides

C. Henneges, S. Huster, A. Zell
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引用次数: 1

Abstract

One key principle of natural immune systems is the extracellular presentation of peptides bound to MHC-II complexes on the cell surface to represent the internal state. The prediction of those peptides that are presented became a current research topic in machine learning, as they may be used as potential vaccines for immunization. In addition the biological immune system (IS) is a learning system in its own right. In this work, we design an artificial immune system (AIS) that is based on observations of the natural immune system to predict MHC-II binding peptides. Our strategy simulates the mutable receptors of T lymphocytes as well as their selection during life time.We model the receptor specificity and binding mode as well as the lymphocyte's influence during an inflammatory response. Finally, our implementation uses the pathogen specificity of T cells to model the prediction problem.
预测MHC-II结合肽的人工t细胞免疫系统
天然免疫系统的一个关键原理是细胞外呈现与细胞表面MHC-II复合物结合的肽,以代表内部状态。这些肽的预测成为当前机器学习的一个研究课题,因为它们可能被用作免疫接种的潜在疫苗。此外,生物免疫系统(IS)本身就是一个学习系统。在这项工作中,我们设计了一个人工免疫系统(AIS),该系统基于对自然免疫系统的观察来预测MHC-II结合肽。我们的策略模拟了T淋巴细胞的可变受体以及它们在生命周期中的选择。我们模拟了受体特异性和结合模式,以及淋巴细胞在炎症反应中的影响。最后,我们的实现利用T细胞的病原体特异性来建模预测问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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