Copyright
©The Author(s) 2016.
World J Gastroenterol. Jul 28, 2016; 22(28): 6373-6384
Published online Jul 28, 2016. doi: 10.3748/wjg.v22.i28.6373
Published online Jul 28, 2016. doi: 10.3748/wjg.v22.i28.6373
Figure 2 Two different tumour microenvironments of different molecular subgroups of gastric cancer.
A: Example of a strong immunogenic tumour with increased antigen presentation and immune checkpoints expression, more TILs and other effector immune cells infiltration into the tumour; B: Example of a weak anti-tumour immune response with less antigen expression, less TILs and other effector immune cell infiltration into tumour and increased numbers of immunosuppressive cells; C: Schematic diagram representing poor defences from a conspicuous tumour with vigorous immune response; D: Schematic diagram representing good defences from a less conspicuous tumour with minimal immune response. MDSC: Myeloid-derived suppressor cell; TAM: Tumour associate macrophages; Treg: T regulatory cell; Th17: T helper cell-17; ECM: Extracellular matrix; MHC: Major histocompatibility complex; TCR: T-cell receptor.
- Citation: Wang M, Busuttil RA, Pattison S, Neeson PJ, Boussioutas A. Immunological battlefield in gastric cancer and role of immunotherapies. World J Gastroenterol 2016; 22(28): 6373-6384
- URL: https://www.wjgnet.com/1007-9327/full/v22/i28/6373.htm
- DOI: https://dx.doi.org/10.3748/wjg.v22.i28.6373