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T细胞耗竭动态对肿瘤-免疫相互作用及肿瘤生长的影响

The Impact of T-cell Exhaustion Dynamics on Tumour-Immune Interactions and Tumour Growth.

作者信息

Lai Nicholas, Farman Alexis, Byrne Helen M

机构信息

Wolfson Centre for Mathematical Biology, Mathematical Institute, University of Oxford, Oxford, OX2 6GG, UK.

Department of Mathematics, University College London, London, WC1E 6BT, UK.

出版信息

Bull Math Biol. 2025 Apr 2;87(5):61. doi: 10.1007/s11538-025-01433-1.

Abstract

Tumours evade immune surveillance through a number of different immunosuppressive mechanisms. One such mechanism causes cytotoxic T-cells, a major driving force of the immune system, to differentiate to a state of 'exhaustion', rendering them less effective at killing tumour cells. We present a structured mathematical model that focuses on T-cell exhaustion and its effect on tumour growth. We compartmentalise cytotoxic T-cells into discrete subgroups based on their exhaustion level, which affects their ability to kill tumour cells. We show that the model reduces to a simpler system of ordinary differential equations (ODEs) that describes the time evolution of the total number of T-cells, their mean exhaustion level and the total number of tumour cells. Numerical simulations of the model equations reveal how the exhaustion distribution of T-cells changes over time and how it influences the tumour's growth dynamics. Complementary bifurcation analysis shows how altering key parameters significantly reduces the tumour burden, highlighting exhaustion as a promising target for immunotherapy. Finally, we derive a continuum approximation of the discrete ODE model, which admits analytical solutions that provide complementary insight into T-cell exhaustion dynamics and their effect on tumour growth.

摘要

肿瘤通过多种不同的免疫抑制机制逃避免疫监视。其中一种机制会使作为免疫系统主要驱动力的细胞毒性T细胞分化为“耗竭”状态,使其在杀伤肿瘤细胞方面的效果降低。我们提出了一个结构化的数学模型,该模型聚焦于T细胞耗竭及其对肿瘤生长的影响。我们根据细胞毒性T细胞的耗竭水平将其划分为不同的离散亚群,而耗竭水平会影响它们杀伤肿瘤细胞的能力。我们表明,该模型可简化为一个更简单的常微分方程(ODE)系统,该系统描述了T细胞总数、其平均耗竭水平和肿瘤细胞总数随时间的演变。对模型方程的数值模拟揭示了T细胞的耗竭分布如何随时间变化以及它如何影响肿瘤的生长动态。互补的分岔分析表明,改变关键参数如何显著减轻肿瘤负担,突出了耗竭作为免疫治疗的一个有前景的靶点。最后,我们推导了离散ODE模型的连续近似,该近似允许有解析解,从而为T细胞耗竭动态及其对肿瘤生长的影响提供了互补的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0165/11965189/91a73a05e23e/11538_2025_1433_Fig1_HTML.jpg

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