©The Author(s) 2016.
World J Gastroenterol. Sep 7, 2016; 22(33): 7440-7452
Published online Sep 7, 2016. doi: 10.3748/wjg.v22.i33.7440
Published online Sep 7, 2016. doi: 10.3748/wjg.v22.i33.7440
Table 1 Rationales of each combination therapy
| Treatments | Rationales | Concerns |
| Checkpoint inhibitor plus cytotoxic agents | Enhance cellular immunity | Efficacy may be influenced by timing when cytotoxic agents add |
| Augment dendritic cell maturation | Severe myelosupression may interrupt immune checkpoint therapy | |
| Reduce MDSC and Tregs | ||
| Decreases CAF | ||
| Combination with checkpoint inhibitors | Activate tumor immunity by different mannar | ir AE will increase |
| Provide synergy efficacy even in immune resistant tumor | ||
| Checkpoint inhibitor plus T cells stimulate agents | Activate tumor immunity by different mannar | Severe AE including cytokine storm may occur |
| Deactive Tregs | ||
| Checkpoint inhibitor plus cancer vaccine | Increase the presentation of taas | |
| Enhance PD-L1 expression | ||
| Radiotherapy | Enhance cross priming of ctls | Optimal schedule and dose are not established |
| Enhanse abscopal effect |
- Citation: Kimbara S, Kondo S. Immune checkpoint and inflammation as therapeutic targets in pancreatic carcinoma. World J Gastroenterol 2016; 22(33): 7440-7452
- URL: https://www.wjgnet.com/1007-9327/full/v22/i33/7440.htm
- DOI: https://dx.doi.org/10.3748/wjg.v22.i33.7440