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Saturday, June 26, 2021 12:07:25 PM
https://jhoonline.biomedcentral.com/articles/10.1186/s13045-018-0582-8
In summary, we have identified that VIP signaling is a novel and targetable immune checkpoint pathway in PDAC, which when inhibited in combination with checkpoint inhibitors, significantly improves treatment response in mouse PDAC models. As the VIP sequence is conserved across different species including mouse and human, and since we have observed VIPR antagonists stimulate proliferation of human T cells, there is an increased potential for clinical translation of VIPR antagonists in the treatment of human PDAC.
https://cancerres.aacrjournals.org/content/80/16_Supplement/5571
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