Lai Nicholas, Farman Alexis, Byrne Helen M
Wolfson Centre for Mathematical Biology, Mathematical Institute, University of Oxford, Oxford, OX2 6GG, UK.
Department of Mathematics, University College London, London, WC1E 6BT, UK.
Bull Math Biol. 2025 Apr 2;87(5):61. doi: 10.1007/s11538-025-01433-1.
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.
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。