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Title: Regulation of PD-L1 expression is a novel facet of cyclic-AMP-mediated immunosuppression.

Authors: Sasi, Binu; Ethiraj, Purushoth; Myers, Jamie; Lin, An-Ping; Jiang, Shoulei; Qiu, Zhijun; Holder, Kenneth N; Aguiar, Ricardo C T

Published In Leukemia, (2021 07)

Abstract: Cyclic-AMP (cAMP) exerts suppressive effects in the innate and adaptive immune system. The PD-1/PD-L1 immune checkpoint downregulates T-cell activity. Here, we examined if these two immunosuppressive nodes intersect. Using normal and malignant lymphocytes from humans, and the phosphodiesterase 4b (Pde4b) knockout mouse, we found that cAMP induces PD-L1 transcription and protein expression. Mechanistically, we discovered that the cAMP effectors PKA and CREB induce the transcription/secretion of IL-10, IL-8, and IL-6, which initiate an autocrine loop that activates the JAK/STAT pathway and ultimately increase PD-L1 expression in the cell surface. This signaling axis is disarmed at two specific nodes in subsets of diffuse large B-cell lymphoma, which may help explain the variable PD-L1 expression in these tumors. In vivo, we found that despite its immunosuppressive attributes, the PDE4 inhibitor roflumilast did not decrease the clinical activity of checkpoint inhibitors, an important clinical observation given the approved use of these agents in multiple diseases. In summary, we discovered that PD-L1 induction is a part of the repertoire of immunosuppressive actions mediated by cAMP, defined a cytokine-mediated autocrine loop that executes this action and, reassuringly, showed that PDE4 inhibition does not antagonize immune checkpoint blockade in an in vivo syngeneic lymphoma model.

PubMed ID: 33299141 Exiting the NIEHS site

MeSH Terms: Aminopyridines/pharmacology; Animals; B7-H1 Antigen/genetics*; Benzamides/pharmacology; Cell Line, Tumor; Cyclic AMP/genetics*; Cyclic Nucleotide Phosphodiesterases, Type 4/genetics; Cyclopropanes/pharmacology; Gene Expression Regulation, Neoplastic/drug effects; Gene Expression Regulation, Neoplastic/genetics; Humans; Immune Tolerance/drug effects; Immune Tolerance/genetics*; Lymphocyte Activation/drug effects; Lymphocyte Activation/genetics; Lymphoma, Large B-Cell, Diffuse/drug therapy; Lymphoma, Large B-Cell, Diffuse/genetics; Mice; Mice, Knockout; Phosphodiesterase 4 Inhibitors/pharmacology; Signal Transduction/drug effects; Signal Transduction/genetics

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