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Phosphodiesterase-5 inhibition collaborates with vaccine-based immunotherapy to reprogram myeloid cells in pancreatic ductal adenocarcinoma
Nicole E. Gross, Zhehao Zhang, Jacob T. Mitchell, Soren Charmsaz, Alexei G. Hernandez, Erin M. Coyne, Sarah M. Shin, Diana Carolina Vargas Carvajal, Dimitrios N. Sidiropoulos, Yeonju Cho, Guanglan Mo, Xuan Yuan, Courtney Cannon, Jayalaxmi Suresh Babu, Melissa R. Lyman, Todd Armstrong, Luciane T. Kagohara, Katherine M. Bever, Dung T. Le, Elizabeth M. Jaffee, Elana J. Fertig, Won Jin Ho
Nicole E. Gross, Zhehao Zhang, Jacob T. Mitchell, Soren Charmsaz, Alexei G. Hernandez, Erin M. Coyne, Sarah M. Shin, Diana Carolina Vargas Carvajal, Dimitrios N. Sidiropoulos, Yeonju Cho, Guanglan Mo, Xuan Yuan, Courtney Cannon, Jayalaxmi Suresh Babu, Melissa R. Lyman, Todd Armstrong, Luciane T. Kagohara, Katherine M. Bever, Dung T. Le, Elizabeth M. Jaffee, Elana J. Fertig, Won Jin Ho
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Research Article Immunology Oncology

Phosphodiesterase-5 inhibition collaborates with vaccine-based immunotherapy to reprogram myeloid cells in pancreatic ductal adenocarcinoma

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Abstract

Pancreatic ductal adenocarcinoma (PDAC) is highly lethal and resistant to immunotherapy. Although immune recognition can be enhanced with immunomodulatory agents including checkpoint inhibitors and vaccines, few patients experience clinical efficacy because the tumor immune microenvironment (TiME) is dominated by immunosuppressive myeloid cells that impose T cell inhibition. Inhibition of phosphodiesterase-5 (PDE5) was reported to downregulate metabolic regulators arginase and inducible NOS in immunosuppressive myeloid cells and enhance immunity against immune-sensitive tumors, including head and neck cancers. We show for the first time to our knowledge that combining a PDE5 inhibitor, tadalafil, with a mesothelin-specific vaccine, anti–programmed cell death protein 1, and anti–cytotoxic T lymphocyte–associated protein 4 yields antitumor efficacy even against immune-resistant PDAC. To determine immunologic advantages conferred by tadalafil, we profiled the TiME using mass cytometry and single-cell RNA-sequencing analysis with Domino to infer intercellular signaling. Our analyses demonstrated that tadalafil reprograms myeloid cells to be less immunosuppressive. Moreover, tadalafil synergized with the vaccine, enhancing T cell activation including mesothelin-specific T cells. Tadalafil treatment was also associated with myeloid/T cell signaling axes important for antitumor responses (e.g., Cxcr3, Il12). Our study shows that PDE5 inhibition combined with vaccine-based immunotherapy promotes pro-inflammatory states of myeloid cells, activation of T cells, and enhanced myeloid/T cell crosstalk to yield antitumor efficacy against immune-resistant PDAC.

Authors

Nicole E. Gross, Zhehao Zhang, Jacob T. Mitchell, Soren Charmsaz, Alexei G. Hernandez, Erin M. Coyne, Sarah M. Shin, Diana Carolina Vargas Carvajal, Dimitrios N. Sidiropoulos, Yeonju Cho, Guanglan Mo, Xuan Yuan, Courtney Cannon, Jayalaxmi Suresh Babu, Melissa R. Lyman, Todd Armstrong, Luciane T. Kagohara, Katherine M. Bever, Dung T. Le, Elizabeth M. Jaffee, Elana J. Fertig, Won Jin Ho

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Figure 3

Myeloid and cytotoxic T cell–focused CyTOF profiling of KPCY 6419c5 tumors from mice treated with vaccine and a 7-day delay in tadalafil treatment.

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Myeloid and cytotoxic T cell–focused CyTOF profiling of KPCY 6419c5 tumo...
(A) Mice were injected with KPCY 6419c5 cells subcutaneously in the right hind limb on day 0, then vaccinated with mesothelin expressing listeria vaccine or control vaccine on day 3. Starting on day 10, mice were treated intravenously with tadalafil or PBS 3 times until tumor harvest on day 17. Harvested tumors were dissociated into single cells, which underwent CyTOF staining or CD45+ enrichment for scRNA-Seq. (B) Clustering heatmap showing macrophage subsets based on relative staining intensities of canonical subtyping markers. Mac, macrophage. (C and D) Boxplots showing abundances of selected clusters calculated as a percentage of all CD45+ cells (n = 3). VEH, vehicle; TAD, tadalafil; MLIST, mesothelin listeria; MLIST_TAD, mesothelin listeria + tadalafil. (E) Clustering heatmap showing CD8+ T cell subsets based on relative staining intensities of canonical subtyping markers. Klick_Tc, Klickmer+ cytotoxic T cell; Tc_Ex, exhausted cytotoxic T cell; Tc_CM, central memory cytotoxic T cell; Tc_KLRG1, KLRG1+ cytotoxic T cell. (F and G) Boxplots showing abundances of Klickmer+ CD8+ T cells calculated as a percentage of all CD45+ cells (n = 7, 8, for vaccine no and yes groups, respectively) (n = 3 for MLIST & MLIST_TAD). (H) Violin plots of MMIs of ICOS, T-bet, PD-1, and LAG3 in selected CD8+ T cell clusters. For FDR-adjusted P values: *P ≤ 0.05, **P ≤ 0.001, ***P ≤ 0.001, for unadjusted P values: #P ≤ 0.05, ##P ≤ 0.001 by 2-tailed Student’s t test for C, D, F, and G and Wilcoxon’s test for H.

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