作者
Pat Gulhati,Aislyn Schalck,Shan Jiang,Xiaoying Shang,Chang‐Jiun Wu,Pingping Hou,Sharia Hernández Ruiz,Luisa M. Solis,Edwin R. Parra,Haoqiang Ying,Jincheng Han,Prasenjit Dey,Haoyan Li,Pingna Deng,Emi Sei,Dean Y. Maeda,John A. Zebala,Denise J. Spring,Michael P. Kim,Huamin Wang,Anirban Maitra,Dirk F. Moore,Karen Clise-Dwyer,Y. Alan Wang,Nicholas Navin,Ronald A. DePinho
摘要
Pancreatic ductal adenocarcinoma (PDAC) is considered non-immunogenic, with trials showing its recalcitrance to PD1 and CTLA4 immune checkpoint therapies (ICTs). Here, we sought to systematically characterize the mechanisms underlying de novo ICT resistance and to identify effective therapeutic options for PDAC. We report that agonist 41BB and antagonist LAG3 ICT alone and in combination, increased survival and antitumor immunity, characterized by modulating T cell subsets with antitumor activity, increased T cell clonality and diversification, decreased immunosuppressive myeloid cells and increased antigen presentation/decreased immunosuppressive capability of myeloid cells. Translational analyses confirmed the expression of 41BB and LAG3 in human PDAC. Since single and dual ICTs were not curative, T cell-activating ICTs were combined with a CXCR1/2 inhibitor targeting immunosuppressive myeloid cells. Triple therapy resulted in durable complete responses. Given similar profiles in human PDAC and the availability of these agents for clinical testing, our findings provide a testable hypothesis for this lethal disease.