The re-polarisation of M2 and M1 macrophages and its role on cancer outcomes

被引:60
作者
den Breems, Nicoline Y. [1 ,2 ,3 ]
Eftimie, Raluca [2 ]
机构
[1] Lincoln Univ, C fACS, Lincoln 7476, New Zealand
[2] Univ Dundee, Div Math, Dundee DD1 4HN, Scotland
[3] Univ Dundee, Div Canc Res, Dundee DD1 9SY, Scotland
基金
英国工程与自然科学研究理事会;
关键词
Cancer modelling; M1 and M2 macrophages; Th1 and Th2 immune cells; TUMOR-ASSOCIATED MACROPHAGES; MATHEMATICAL-MODEL; T-CELLS; SURVIVAL; IMMUNOTHERAPY; PROGRESSION; CD4(+); GROWTH; ANGIOGENESIS; ACTIVATION;
D O I
10.1016/j.jtbi.2015.10.034
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The anti-tumour and pro-tumour roles of Th1/Th2 immune cells and M1/M2 macrophages have been documented by numerous experimental studies. However, it is still unknown how these immune cells interact with each other to control tumour dynamics. Here, we use a mathematical model for the interactions between mouse melanoma cells, Th2/Th1 cells and M2/M1 macrophages, to investigate the unknown role of the re-polarisation between M1 and M2 macrophages on tumour growth. The results show that tumour growth is associated with a type-II immune response described by large numbers of Th2 and M2 cells. Moreover, we show that (i) the ratio k of the transition rates k(12) (for the re-polarisation M1 -> M2) and k(21) (for the re-polarisation M2 -> M1) is important in reducing tumour population, and (ii) the particular values of these transition rates control the delay in tumour growth and the final tumour size. We also perform a sensitivity analysis to investigate the effect of various model parameters on changes in the tumour cell population, and confirm that the ratio k alone and the ratio of M2 and M1 macrophage populations at earlier times (e.g., day 7) cannot always predict the final tumour size. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:23 / 39
页数:17
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