Department of Mathematics & Computer Science, University of Catania, V.le A Doria 6, 95125 Catania, Italy.
Comput Math Methods Med. 2012;2012:850754. doi: 10.1155/2012/850754. Epub 2012 Jun 3.
We present a mathematical model developed to reproduce the immune response entitled with the combined administration of activated OT1 cytotoxic T lymphocytes (CTLs) and Anti-CD137 monoclonal antibodies. The treatment is directed against melanoma in B16 OVA mouse models exposed to a specific immunotherapy strategy. We model two compartments: the injection point compartment where the treatment is administered and the skin compartment where melanoma tumor cells proliferate. To model the migration of OT1 CTLs and antibodies from the injection to the skin compartment, we use delay differential equations (DDEs). The outcomes of the mathematical model are in good agreement with the in vivo results. Moreover, sensitivity analysis of the mathematical model underlines the key role of OT1 CTLs and suggests that a possible reduction of the number of injected antibodies should not affect substantially the treatment efficacy.
我们提出了一个数学模型,旨在重现联合给予激活的 OT1 细胞毒性 T 淋巴细胞(CTL)和抗 CD137 单克隆抗体的免疫反应。该治疗针对的是在接受特定免疫治疗策略的 B16OVA 小鼠模型中暴露的黑色素瘤。我们对两个隔室进行建模:注射部位隔室,其中给予治疗,以及皮肤隔室,其中黑色素瘤肿瘤细胞增殖。为了对 OT1 CTL 和抗体从注射部位到皮肤隔室的迁移进行建模,我们使用时滞微分方程(DDE)。数学模型的结果与体内结果非常吻合。此外,对数学模型的敏感性分析强调了 OT1 CTL 的关键作用,并表明减少注射的抗体数量不太可能会对治疗效果产生实质性影响。