Targeting T cell checkpoints and myeloid suppressor cells is effective in pancreatic cancer
- PMID: 36639509
- DOI: 10.1038/s43018-022-00501-y
Targeting T cell checkpoints and myeloid suppressor cells is effective in pancreatic cancer
Comment on
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Targeting T cell checkpoints 41BB and LAG3 and myeloid cell CXCR1/CXCR2 results in antitumor immunity and durable response in pancreatic cancer.Nat Cancer. 2023 Jan;4(1):62-80. doi: 10.1038/s43018-022-00500-z. Epub 2022 Dec 30. Nat Cancer. 2023. PMID: 36585453 Free PMC article.
References
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- Bear, A. S., Vonderheide, R. H. & O’Hara, M. H. Challenges and opportunities for pancreatic cancer immunotherapy. Cancer Cell 38, 788–802 (2020). A review article that describes strategies that may be rationally combined to overcome immune resistance in PDAC. - DOI
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- O’Reilly, E. M. et al. Durvalumab with or without tremelimumab for patients with metastatic pancreatic ductal adenocarcinoma. JAMA Oncol. 5, 1431–1438 (2019). This paper reports the lack of clinical efficacy of anti-PD1 and anti-CTLA4 immunotherapy in PDAC. - DOI
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- Steele, C. W. et al. CXCR2 inhibition profoundly suppresses metastases and augments immunotherapy in pancreatic ductal adenocarcinoma. Cancer Cell 29, 832–845 (2016). This paper provides the pre-clinical rationale for targeting CXCR2 on myeloid cells in combination with immunotherapy in PDAC. - DOI
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- Van Der Leun, A. M., Thommen, D. S. & Schumacher, T. N. CD8+ T cell states in human cancer: insights from single cell analysis. Nat. Rev. Cancer 20, 218–232 (2020). A review article that describes the relationship between various T cell states and therapeutic response to ICT. - DOI
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