Semi mature blood dendritic cells exist in patients with ductal pancreatic adenocarcinoma owing to inflammatory factors released from the tumor

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Abstract

Background: Much evidence exists regarding the fact that blood DCs, both myeloid DCs (MDCs) and plasmacytoid DCs (PDCs), are negatively affected in different types of cancer, with both reduced numbers and impaired functionality. Functional impairment of DCs in patients with pancreatic ductal adenocarcinoma (PDAC), may contribute to the poor clinical outcome. The aim of this study was to examine the effects PDAC had on blood DCs and elucidate the underlying mechanism responsible for the DC impairment. Methodology/Principal Findings: We examined the systemic influence PDAC exerted on blood DCs by ex vivo measuring numerous activation and maturation markers expressed on these cells. Furthermore, the effect patient plasma and the inflammatory factors CXCL8 and PGE2 had on purified MDCs and PDCs from healthy donors was assessed and compared to the DCs existing in PDAC patients. We found a partial maturation of the blood MDCs and PDCs in PDAC patients with significantly enhanced expression of CD83, CD40, B7H3, PDL-1, CCR6, and CCR7 and decreased expression of ICOSL, and DCIR. These changes lead to impairment in their immunostimulatory function. Furthermore, chronic pancreatitis gave rise to DCs with similar semi-mature phenotype as seen in PDAC. Low expression of ICOSL was associated with poor prognosis. We found that the mechanism underlying this semi-maturation of DCs was inflammatory factors existing in the PDAC patients' plasma. Of note, PGE2, which is elevated PDAC patient plasma, was one contributing factor to the changes seen in MDCs and PDCs phenotype. Conclusion/Significance: Our findings point to a role for the systemic inflammation in transforming blood MDCs and PDCs into semi-mature cells in PDAC patients and we show a correlation between maturation status and clinical outcome. Thus, means to preserve a functional blood DC compartment in PDAC patients by diminishing the inflammation could facilitate their ability to control the disease and improve survival. © 2010 Tjomsland et al.

Figures

  • Figure 1. Decreased levels of MDCs and PDCs in patients with PDAC. PBMCs isolated from individuals with pancreatic duct adenocarcinoma (PDAC) (1 week pre and 12 weeks post surgery) and healthy age matched volunteers were analyzed for DC levels by flow cytometry. The PBMCs were stained with Linage cocktail, HLA DR, CD11c, and CD123 direct conjugated mabs to distinguish all DC subsets from the rest of the cells. The DC levels were calculated from the total amount of PBMCs and compared between the different groups using nonparametric Wilcoxon signed rank test used for paired data and Mann– Whitney test for calculation of p values. Statistically significant differences between individuals with PDAC and healthy controls are indicated as; * = p,0.05, ** = p,0.005, *** = p,0.001. doi:10.1371/journal.pone.0013441.g001
  • Figure 2. Increased levels of activation markers CD83 and CD40 on blood DCs in patients with PDAC. Blood MDCs (HLA DR+CD11c+Lin2) and PDCs (HLA DR+CD123+Lin2) were detected in PBMCs obtained from PDAC patients pre (1 week) and post (12 weeks) surgery and healthy age matched individuals. Both DC subsets were investigated for the expression of the maturation marker CD83 (A), co-stimulatory molecule CD40 (B), and HLA DR (C). Mean fluorescence intensity (MFI) and percentage (%) of positive MDCs and PDCs and compared between the different groups using nonparametric Wilcoxon signed rank test used for paired data and Mann–Whitney test for calculation of p values. Statistically significant differences between individuals with PDAC and healthy controls are indicated as; * = p,0.05, ** = p,0.005, *** = p,0.001. doi:10.1371/journal.pone.0013441.g002
  • Figure 3. The C type lectin DCIR was down regulated on MDCs and PDCs in PDAC patients. Dendritic cell subsets, MDCs (HLA DR+CD11c+Lin2) and PDCs (HLA DR+CD123+Lin2), were distinguished form PBMCs obtained from PDAC patients pre (1 week) and post (12 weeks) surgery and age matched control individuals by flow cytometry. Changes in DC phenotype were detected using direct conjugated antibody for dendritic cell immunoreceptor (DCIR). Mean fluorescence intensity (MFI) values from the patients included in the different groups were compared using nonparametric Wilcoxon signed rank test, used for paired data and Mann–Whitney test for calculation of p values. Statistically significant differences between individuals with PDAC and healthy controls are indicated as; * = p,0.05, ** = p,0.005, *** = p,0.001. doi:10.1371/journal.pone.0013441.g003
  • Figure 4. Increased B7 family expression profile on MDCs and PDCs in patients with PDAC. Blood MDCs (HLA DR+CD11c+Lin2) and PDCs (HLA DR+CD123+Lin2) were detected in PBMCs obtained from PDAC patients pre (1 week) and post (12 weeks) surgery and healthy age matched individuals. Both DC subsets were investigated for the expression of co-stimulatory molecules from B7 family using direct conjugated antibodies against PDL-1 (A), ICOSL (B) and B7H3 (C) and analyzed using 8 color flow cytometry. Mean fluorescence intensity (MFI) values or present positive MDCs and PDCs were compared between the different groups using nonparametric Wilcoxon signed rank test used for paired data and Mann– Whitney test for calculation of p values. Statistically significant differences between individuals with PDAC and healthy controls are indicated as; * = p,0.05, ** = p,0.005, *** = p,0.001. doi:10.1371/journal.pone.0013441.g004
  • Figure 5. Chemokine receptor expression profile on MDC and PDCs in patients with PDAC. Blood MDCs (HLA DR+CD11c+Lin2) and PDCs (HLA DR+CD123+Lin2) from PDAC patients pre (one week) and post (12 weeks) surgery were compared to age matched controls. The DC subsets from each group were stained using direct conjugated antibodies against CCR2 (A), CCR5 (B), CCR6 (C), and CCR7 (D) and detected by multi-color flow cytometry. Mean fluorescence intensity (MFI) values or the amount positive MDCs and PDCs in percentage were compared between the different groups using nonparametric Wilcoxon signed rank test used for paired data and Mann–Whitney test for calculation of p values. Statistically significant differences between individuals with PDAC and healthy controls are indicated as; * = p,0.05, ** = p,0.005, *** = p,0.001. doi:10.1371/journal.pone.0013441.g005
  • Figure 6. Blood DCs from chronic pancreatitis patients exhibited a similar semi-mature phenotype seen in PDAC patients. Dendritic cell subsets, MDCs (HLA DR+CD11c+Lin2) and PDCs (HLA DR+CD123+Lin2), were distinguished form PBMCs obtained from chronic pancreatitis (CP) patients (N = 5) and age matched control individuals by flow cytometry. Changes in DC phenotype were detected using direct conjugated antibody for CD40, CD83, CCR2, CCR6, CCR5, CCR7, PDL-1, ICOSL, DCIR, and B7H3. Mean fluorescence intensity (MFI) values from the patients included in the different groups were compared using nonparametric Wilcoxon signed rank test, used for paired data and Mann–Whitney test for calculation of p values. Statistically significant differences between individuals with CP and healthy controls are indicated as; * = p,0.05, ** = p,0.005, *** = p,0.001. doi:10.1371/journal.pone.0013441.g006
  • Figure 7. MDC and PDC in PDAC patients have impaired immunostimulatory function. A–B) Immunostimulatory capacity of blood DC tested by mixed leukocyte reaction (MLR). MDCs (A) and PDCs (B) purified from PDAC patients (N = 6) or healthy controls (N = 6) were cocultured with allogeneic T cells for 5 days and T cell proliferation assessed by 3H-Thymine incorporation. Comparison of stimulatory capacity was assessed by dividing the counts per minute (CPM) of patients with the mean CPM of controls and the CPM of the controls with the mean CPM of the patients for each plate analyzed. Statistical significance was determined by Mann–Whitney test for calculation of p values. * = p,0.05, ** = p,0.005. doi:10.1371/journal.pone.0013441.g007
  • Figure 8. Low expression levels of ICOSL and CCR2 correlated to poor prognosis in PDAC patients. Median fluorescence intensity (MFI) levels for ICOSL on MDCs and PDCs pre surgery were correlated to patient survival time. (A) The patients were divided into two groups, one group consisting of patients surviving more than two years (N = 11) and the second group of patients surviving less than two years (N = 13). Comparison of the survival between the PDAC patient group with the lowest (scattered line) (N = 12) and highest (N = 12) mean fluorescence intensity (MFI) levels of ICOSL for (B) MDCs (#641MFI and .641MFI), (C) PDCs (#598MFI and .598MFI) and MFI levels of CCR2 for (D) PDCs (#601.5MFI and .601.5MFI) pre surgery. Long-rank (Mantel-Cox) test was used for calculation of p values. * = p,0.05, ** = p,0.005. doi:10.1371/journal.pone.0013441.g008

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Tjomsland, V., Spångeus, A., Sandström, P., Borch, K., Messmer, D., & Larsson, M. (2010). Semi mature blood dendritic cells exist in patients with ductal pancreatic adenocarcinoma owing to inflammatory factors released from the tumor. PLoS ONE, 5(10). https://doi.org/10.1371/journal.pone.0013441

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