Several CAF-derived factors have been shown to recruit macrophages into tumours and polarise them towards an M2 tumour promoting phenotype, including CXCL12 and MCP-1 (monocyte chemotactic protein 1) [93, 94], with M2 macrophages having suppressive effect on T-cells mediated by increased expression of arginase I, interleukin-10 and TGF-β [92]. This evidence concerns the gene IL10 and neoplasm.