Department of Bioengineering, University of Louisville, KY, USA.
Department of Bioengineering, University of Louisville, KY, USA; James Graham Brown Cancer Center, University of Louisville, KY, USA; Department of Pharmacology & Toxicology, University of Louisville, KY, USA.
J Theor Biol. 2019 May 21;469:47-60. doi: 10.1016/j.jtbi.2019.03.002. Epub 2019 Mar 2.
The anti-tumor activity of the immune system is increasingly recognized as critical for the mounting of a prolonged and effective response to cancer growth and invasion, and for preventing recurrence following resection or treatment. As the knowledge of tumor-immune cell interactions has advanced, experimental investigation has been complemented by mathematical modeling with the goal to quantify and predict these interactions. This succinct review offers an overview of recent tumor-immune continuum modeling approaches, highlighting spatial models. The focus is on work published in the past decade, incorporating one or more immune cell types and evaluating immune cell effects on tumor progression. Due to their relevance to cancer, the following immune cells and their combinations are described: macrophages, Cytotoxic T Lymphocytes, Natural Killer cells, dendritic cells, T regulatory cells, and CD4+ T helper cells. Although important insight has been gained from a mathematical modeling perspective, the development of models incorporating patient-specific data remains an important goal yet to be realized for potential clinical benefit.
免疫系统的抗肿瘤活性正日益被认为对于肿瘤生长和侵袭的长期有效反应的产生以及切除或治疗后的复发预防至关重要。随着对肿瘤-免疫细胞相互作用的认识不断提高,实验研究得到了数学建模的补充,其目的是对这些相互作用进行量化和预测。这篇简洁的综述概述了最近的肿瘤-免疫连续体建模方法,重点介绍了空间模型。重点是过去十年发表的工作,其中纳入了一种或多种免疫细胞类型,并评估了免疫细胞对肿瘤进展的影响。由于与癌症的相关性,以下免疫细胞及其组合进行了描述:巨噬细胞、细胞毒性 T 淋巴细胞、自然杀伤细胞、树突状细胞、调节性 T 细胞和 CD4+辅助性 T 细胞。尽管从数学建模的角度已经获得了重要的见解,但对于潜在的临床益处,开发纳入患者特定数据的模型仍然是一个尚未实现的重要目标。