Subcutaneous Injections of the Mannose-Sensitive Hemagglutination Pilus Strain of Pseudomonas aeruginosa Stimulate Host Immunity, Reduce Bladder Cancer Size and Improve Tumor Survival in Mice

Cell Biochem Biophys. 2015 Sep;73(1):245-52. doi: 10.1007/s12013-015-0611-y.

Abstract

We wished to evaluate the effects of Pseudomonas aeruginosa (mannose-sensitive hemagglutination pilus strain, PA-MSHA) as an immunostimulating and anti-tumor agent for treatment of bladder cancer. Immunostimulating effects were assessed by the in vitro proliferation assay of murine splenic lymphocytes. Anti-tumor effects were studied in a subcutaneous tumor model established in female C57BL/6 mice using the MB49 bladder cell line. These mice received subcutaneous injections of normal saline (control group) or PA-MSHA (high, medium, or low dose, respectively, 1.6-2.0 × 10(9), 3.2- .0 × 10(8), 6.4-8.0 × 10(7) CFU/ml) twice a week for 3 weeks. Mice survival, tumor volume, vascular endothelial growth factor (VEGF) expression, microvessel density (MVD), serum levels of TNF-α and IFN-γ, and blood CD4(+) /CD8(+) counts were the study outcomes. We observed that PA-MSHA promoted the growth of splenic lymphocytes in vitro. In the murine tumor model, PA-MSHA prolonged mice survival and reduced tumor growth. Furthermore, VEGF and MVD were also diminished by PA-MSHA. Mice that received high and medium dose of PA-MSHA had significantly higher serum levels of IFN-γ and TNF-α (days 21 and 28), and higher levels of CD4(+) /CD8(+) cells (days 21 and 28). In conclusion, PA-MSHA exerts beneficial effects on increasing proliferation of murine splenic lymphocytes in vitro and inhibits the growth of bladder tumor in a murine model. Therefore, PA-MSHA may be useful an immunostimulating and anti-tumor agent for bladder cancer therapy.

Keywords: Bladder tumor; Cytokines; Mice; Microvessel density; Pseudomonas aeruginosa; Vascular endothelial growth factor.

MeSH terms

  • Animals
  • CD4-CD8 Ratio
  • Cell Line, Tumor
  • Cell Proliferation
  • Cells, Cultured
  • Female
  • Fimbriae Proteins / immunology
  • Fimbriae Proteins / therapeutic use*
  • Immunotherapy*
  • Interferon-gamma / blood
  • Lymphocytes / immunology*
  • Lymphocytes / physiology
  • Mice
  • Mice, Inbred C57BL
  • Neovascularization, Pathologic / therapy
  • Pseudomonas aeruginosa / immunology*
  • Spleen / cytology
  • Tumor Necrosis Factor-alpha / blood
  • Urinary Bladder Neoplasms / therapy*
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Tumor Necrosis Factor-alpha
  • Vascular Endothelial Growth Factor A
  • mannosesensitive haemagglutinin, Pseudomonas aeruginosa
  • Fimbriae Proteins
  • Interferon-gamma