期刊
CLINICAL CANCER RESEARCH
卷 27, 期 23, 页码 6287-6297出版社
AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-18-0900
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资金
- NCI [1R37CA237384-01A1]
- CPRIT [RP200173]
- V Foundation Translational Award
- Andrew Sabin Family Fellowship
- Philantropic Moonshot Programs (MDACC)
- NIH [R01 CA236118, CA236949]
- DOD PRCRP [CA181486]
- Neuroendocrine Tumor Research Foundation-AACR Grant [18-6033-MAZU]
- Andrew Sabin Family Foundation
- CPRIT Scholar in Cancer Research [RR160078]
- CDMRP [1102294, CA181486] Funding Source: Federal RePORTER
Pancreatic cancer shows limited efficacy to immunotherapy due to unique factors such as suppressive elements in the tumor microenvironment, barriers imposed by stroma components, T cell exhaustion, possibly wrong immune targets, and microbial factors. Various strategies to overcome these barriers are discussed in the article.
Immunotherapy has dramatically changed the cancer treatment landscape during the past decade, but very limited efficacy has been reported against pancreatic cancer. Several factors unique to pancreatic cancer may explain the resistance: the well-recognized suppressive elements in the tumor microenvironment, the functional and structural barrier imposed by the stroma components, T cell exhaustion, the choice of perhaps the wrong immune targets, and microbial factors including gut dysbiosis and the unexpected presence of tumor microbes. Furthermore, we discuss various strategies to overcome these barriers.
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