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辅助性T淋巴细胞/抗原呈递细胞相互作用的数学建模:抗原加工与呈递修饰方法分析

Mathematical modeling of helper T lymphocyte/antigen-presenting cell interactions: analysis of methods for modifying antigen processing and presentation.

作者信息

Agrawal N G, Linderman J J

机构信息

Department of Chemical Engineering, University of Michigan, Ann Arbor 48109, USA.

出版信息

J Theor Biol. 1996 Oct 21;182(4):487-504. doi: 10.1006/jtbi.1996.0190.

Abstract

Helper T lymphocytes (Th cells) are activated by contact with antigen-presenting cells (APCs) that have processed and presented the appropriate MHC-peptide complexes. Two experimental methods for modifying antigen processing and presentation include altering the properties of the antigen and altering the method of antigen uptake. Mathematical modeling was used to investigate the effects of these two methods on the Th cell response. Two mathematical models were used, one for relating the external antigen concentration to the number of MHC-peptide complexes to the number of bound T cell receptors (TCRs) on the Th cell. Large values of MHC/peptide affinity were predicted to compensate for small values of TCR/MHC-peptide affinity in particular parameter ranges. Similarly, large values of antigen receptor number were predicted to compensate for small values of antigen receptor affinity in particular parameter ranges. Results were shown to agree with a variety of experimental data. In addition, model predictions suggest that knowledge of MHC/peptide, TCR/MHC-peptide, and receptor/antigen affinities is not sufficient to accurately describe an experimental system; the kinetic rate constants can dramatically affect antigen processing and presentation, the Th-APC interaction, and the Th cell response. This theoretical approach is useful not only for interpreting experimental data but also for guiding future experiments aimed at manipulating the Th cell response.

摘要

辅助性T淋巴细胞(Th细胞)通过与已处理并呈递适当MHC-肽复合物的抗原呈递细胞(APC)接触而被激活。两种用于改变抗原处理和呈递的实验方法包括改变抗原的性质和改变抗原摄取的方法。使用数学建模来研究这两种方法对Th细胞反应的影响。使用了两个数学模型,一个用于将外部抗原浓度与MHC-肽复合物的数量以及Th细胞上结合的T细胞受体(TCR)的数量联系起来。预测在特定参数范围内,MHC/肽亲和力的高值可补偿TCR/MHC-肽亲和力的低值。同样,预测在特定参数范围内,抗原受体数量的高值可补偿抗原受体亲和力的低值。结果表明与各种实验数据相符。此外,模型预测表明,仅了解MHC/肽、TCR/MHC-肽和受体/抗原亲和力不足以准确描述实验系统;动力学速率常数可显著影响抗原处理和呈递、Th-APC相互作用以及Th细胞反应。这种理论方法不仅有助于解释实验数据,还可指导未来旨在操纵Th细胞反应的实验。

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