Analysis of groundwater ion abnormality and its cause of centralized drinking water sources in Jieshou City, China

Groundwater provides drinking water to city and rural residents; which is also one of the chief water sources for commercial and agricultural activities in Jieshou City. We collected and analyzed the samples of 18 underground water source wells in Jieshou. We investigated whether the water was of acceptable quality and had characteristics that exceeded the standard. This study was conducted to determine the chemical characteristics of groundwater and abnormally high super-standard ions found in groundwater. The hydrogeological conditions of the study area were analyzed through data collection; through sample collection and sample testing, the characteristics and types of water chemistry were analyzed by means of mathematical statistics analysis and the Piper chart. The genesis of water chemistry was discussed using the Gibbs chart and correlation analysis; the proportional coefficient of ion molar concentration was used to judge the source, origin, and forming process of groundwater chemical composition. The results show that the groundwater is classified as marginally alkaline water, with a composition of Na-HCO3. The cations are mainly Na+, and the anions are mainly HCO3−. According to the Ⅲ water standard of groundwater quality standard and comparing the content of each ion, Na+ and F− are the primary abnormal super-standard ions, and ions and compounds are the main occurrence states. The concentrations of Na+ and F− exceed the standard for class Ⅲ water. There was a positive correlation between the abnormal Na+ and F−, and the concentration of F− increased with the increase in monitoring depth. The causes of abnormal ions were mainly determined by the lithology of the aquifer in the study area, and most of them are fluorine-containing rocks, which are transferred into groundwater through leaching or hydration. The enrichment of Na+ and F− is influenced by the local primary geological setting, hydrochemical type, hydrogeological conditions, pH and artificial activities, and the primary geological setting is the main influencing factor

31st Annual Meeting and Associated Programs of the Society for Immunotherapy of Cancer (SITC 2016) : part two

Background The immunological escape of tumors represents one of the main ob- stacles to the treatment of malignancies. The blockade of PD-1 or CTLA-4 receptors represented a milestone in the history of immunotherapy. However, immune checkpoint inhibitors seem to be effective in specific cohorts of patients. It has been proposed that their efficacy relies on the presence of an immunological response. Thus, we hypothesized that disruption of the PD-L1/PD-1 axis would synergize with our oncolytic vaccine platform PeptiCRAd. Methods We used murine B16OVA in vivo tumor models and flow cytometry analysis to investigate the immunological background. Results First, we found that high-burden B16OVA tumors were refractory to combination immunotherapy. However, with a more aggressive schedule, tumors with a lower burden were more susceptible to the combination of PeptiCRAd and PD-L1 blockade. The therapy signifi- cantly increased the median survival of mice (Fig. 7). Interestingly, the reduced growth of contralaterally injected B16F10 cells sug- gested the presence of a long lasting immunological memory also against non-targeted antigens. Concerning the functional state of tumor infiltrating lymphocytes (TILs), we found that all the immune therapies would enhance the percentage of activated (PD-1pos TIM- 3neg) T lymphocytes and reduce the amount of exhausted (PD-1pos TIM-3pos) cells compared to placebo. As expected, we found that PeptiCRAd monotherapy could increase the number of antigen spe- cific CD8+ T cells compared to other treatments. However, only the combination with PD-L1 blockade could significantly increase the ra- tio between activated and exhausted pentamer positive cells (p= 0.0058), suggesting that by disrupting the PD-1/PD-L1 axis we could decrease the amount of dysfunctional antigen specific T cells. We ob- served that the anatomical location deeply influenced the state of CD4+ and CD8+ T lymphocytes. In fact, TIM-3 expression was in- creased by 2 fold on TILs compared to splenic and lymphoid T cells. In the CD8+ compartment, the expression of PD-1 on the surface seemed to be restricted to the tumor micro-environment, while CD4 + T cells had a high expression of PD-1 also in lymphoid organs. Interestingly, we found that the levels of PD-1 were significantly higher on CD8+ T cells than on CD4+ T cells into the tumor micro- environment (p < 0.0001). Conclusions In conclusion, we demonstrated that the efficacy of immune check- point inhibitors might be strongly enhanced by their combination with cancer vaccines. PeptiCRAd was able to increase the number of antigen-specific T cells and PD-L1 blockade prevented their exhaus- tion, resulting in long-lasting immunological memory and increased median survival