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Fig. 1 | Journal of Experimental & Clinical Cancer Research

Fig. 1

From: Tumor immune microenvironment-based therapies in pancreatic ductal adenocarcinoma: time to update the concept

Fig. 1

Interactions between PDAC cells and lymphocytes in TIME. Tumor cells inhibit the normal function of CD8+ effector T cells by upregulating the expression of multiple checkpoint ligands. Tumor cells also inhibited the activation of NK cells, CD4+ T cells, and B cells. By releasing a variety of immunosuppressive factors, tumor cells promote the activation of Tregs and Bregs. All these make the microenvironment present a state of immune exhaustion. Red arrows represent tumor-promoting processes. Pink circles represent possible treatment strategies. TIGIT: T cell immunoreceptor with Ig and ITIM domains; C-FOXP3: cancer Forkhead box protein 3; APC: antigen presenting cell; BTK: Bruton's tyrosine kinase; Breg: regulatory B cell

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