Evaluation of hGM-CSF/hTNFα surface-modified prostate cancer therapeutic vaccine in the huPBL-SCID chimeric mouse model
Journal of Hematology & Oncology volume 8, Article number: 76 (2015)
To validate its efficacy in the context of the human immune system, a novel therapeutic vaccine of hGM-CSF/hTNFα surface-modified PC-3 cells against human prostate cancer was evaluated in the human peripheral blood lymphocytes-severe combined immunodeficiency (huPBL-SCID) chimeric mouse model. The hGM-CSF or/and hTNFα modified vaccines inhibited prostate cancer growth effectively so as to prolong the mouse survival significantly. The splenocytes from the hGM-CSF/hTNFα vaccine-inoculated mice showed the strongest tumor-specific cytotoxicity against PC-3 cells and the highest production of IFNɤ. These features indicated that type 1 protective immune response was induced efficiently against human prostate cancer and further enhanced through synergetic adjuvant effects of hGM-CSF and hTNFα.
Prostate cancer is currently the second leading cause of cancer-related death in elderly men and likely develops into androgen-independent at advanced stages, which is refractory to conventional treatments. Cancer vaccine is a rational option for the treatment of androgen-independent prostate cancer . Cancer immunotherapy is getting more and more important, remarkably evidenced by recent checkpoint blockade or chimeric antigen receptor-engineered T cell-based clinical trials with the impressive efficacy in different types of metastatic cancers [2, 3].
Through simultaneous immobilization of streptavidin-tagged bioactive GM-CSF and TNFα on the biotinylated surface of cancer cells, we previously showed that the resultant cancer vaccines could induce a strong anti-tumor T cell immunity [4–7]. In the current study, human peripheral blood lymphocytes-severe combined immunodeficiency (huPBL-SCID) model was utilized to mimic the human immune system for evaluating the efficacy of these therapeutic vaccines. The materials and methods used in this study are detailed in Additional file 1.
We demonstrated that SA-hGM-CSF or/and SA-hTNFα could be efficiently immobilized on the biotinylated surface of ethanol-fixed PC-3 cells (Additional file 2) and SA-hGM-CSF or/and SA-hTNFα immobilized on the PC-3 cells still retained their bioactivity (Additional file 3).
The PC-3 cells inoculated subcutaneously in nonobese diabetic/severe combined immunodeficiency (NOD/SCID) mice were found to maintain their original tumorigenicity so as to spread into the blood (Additional file 4). There was no phenomenon of immune leakage  in NOD/SCID mice used in this study. The activity of natural killer (NK) cells in the NOD/SCID mice was dramatically reduced by injection of anti-asialo-GM1 antibody (Additional file 5).
Flow cytometry detected human CD4+, CD8+, and CD45+ cells in peripheral blood and human CD45+ cells in spleen of huPBL-SCID mice. IHC staining revealed many human CD4+ and CD8+ lymphocytes present in spleen and fewer human CD4+ and CD8+ lymphocytes in liver tissue 8 weeks after transfer of huPBL. The results indicated that human T lymphocytes were successfully engrafted and homed in appropriate lymphoid organs of huPBL-SCID mice (Additional files 6 and 7).
We tested therapeutic effects of different PC-3 cell vaccines modified with hGM-CSF and/or hTNFα on human prostate cancer in the huPBL-SCID mouse model. Compared with other cancer vaccines, the hGM-CSF/hTNFα doubly modified cancer vaccine significantly inhibited prostate cancer growth in terms of tumor weight (Fig. 1a) and size (Fig. 1b) and effectively prolonged the mice survival (Fig. 1c).
There were more human leukocytes and CD4+ or CD8+ lymphocytes residing in the lymph nodes in the hGM-CSF/hTNFα doubly modified group than in other groups 8 weeks after vaccination (Additional file 8). Similarly, more human CD4+ or CD8+ T lymphocytes were found to infiltrate into the tumor tissues in the hGM-CSF/hTNFα doubly modified group than in other groups (Fig. 2a, b), indicating that the hGM-CSF/hTNFα doubly modified PC-3 cell vaccine could enhance its anti-tumor immunity by increasing the infiltration of human T lymphocytes into the tumors.
We finally analyzed the tumor-specific cytotoxicity of cytotoxic T lymphocytes (CTL) in the spleen and revealed that the GM-CSF/TNFα doubly modified vaccine did establish a stronger tumor-specific T cell immunity than other PC-3 cell vaccines (Fig. 2c). The supernatant from in vitro splenocyte culture in the GM-CSF/TNFα doubly modified group had the highest production of PC-3-specific IFNγ (Fig. 2d). Both results indicated that type 1 protective immunity was induced against the human prostate cancer.
Therefore, our current study provided a solid foundation for potential clinical application of this novel hGM-CSF/hTNFα surface-modified prostate cancer therapeutic vaccine. This unique approach can be easily adopted to generate a personalized whole cancer cell vaccine from individual autologous cancer cells, thereby potentially overcoming cancer antigen heterogeneity [9–11].
human granulocyte-macrophage colony-stimulating factor
human tumor necrosis factor α
human peripheral blood lymphocytes
nonobese diabetic/severe combined immunodeficiency
prostate-specific membrane antigen
enzyme-linked immunosorbent assay
human leukocyte antigen
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This work was supported partly by Chinese National 863 plan (2012AA02A407), The Scientific Research Fund of Ministry of Public Health (201231029), Zhejiang Provincial Major Research Program (2010C13007), Key Science and Technology Innovation Team of Zhejiang Province, the Natural Science Foundation of Zhejiang Province (Y2110580, LY12C07001, LY13H100003, LZ14H260001), Zhejiang Provincial Program for the Cultivation of High-level Innovative Health Talents, Science and Technology Innovation Program for College/University Students in Zhejiang Province (2012R413039, 2012R413041).
The authors declare that they have no competing interests.
SL carried out the vaccine preparation and animal studies, participated in the bioactive assays and immunologic reconstitution, established the tumor models, and drafted the manuscript. ZH carried out tumor-specific cytotoxicity assay and histological and immunohistochemical analysis and participated in establishment of the tumor models. YG participated in the bioactive assays and immunologic reconstitution and helped to draft the manuscript. YC carried out the ELISA. WR participated in the NOD/SCID mouse preparation. LW participated in the design of the study. FY performed the statistical analysis. HG carried out cell culture. LH participated in the animal studies. TZ designed animal studies and participated in the manuscript preparation. JJ participated in the study design and helped to draft the manuscript. JG conceived of the study, participated in its design and coordination, and helped to draft the manuscript. All authors read and approved the final manuscript.
Shouhua Lai, Zhiyong Huang and Yunting Guo contributed equally to this work.
Materials and methods.
Flow cytometric analysis of the modification efficiency of streptavidin (SA)-tagged hGM-CSF and/or hTNFα on the surface of ethanol-fixed and biotinylated PC-3 prostate cancer cell vaccine. Ethanol-fixed PC-3 cells were biotinylated and then incubated with SA-hGM-CSF, SA-hTNFα, or both as described before. The presence of hGM-CSF or/and hTNFα was assessed with allophycocyanin (APC)-labeled anti-hGM-CSF (1:400) or/and fluorescein isothiocyanate (FITC)-labeled anti-hTNFα (1:100) monoclonal antibodies for flow cytometric analysis. Ethanol-fixed PC-3 cells were used as control.
Bioactive assays of hGM-CSF and hTNFα immobilized on the surface of ethanol-fixed PC-3 prostate cancer cell vaccine. Membrane fractions were prepared from the hGM-CSF/hTNFα doubly modified PC-3 cancer cell vaccine as described in materials and methods. (A) Bioactive assay of hGM-CSF immobilized on the surface of ethanol-fixed PC-3 cell vaccine. The proliferative activity of membrane-conjugated hGM-CSF was assessed on TF-1 cells with SA-hGM-CSF/SA-hTNFα un-modified PC-3 cell vaccine as negative control. (B) Bioactive assay of hTNF-α immobilized on the surface of ethanol-fixed PC-3 cell vaccine. The cytotoxic activity of membrane-conjugated hTNFα was assessed on L929 cells with hGM-CSF/hTNFα un-modified PC-3 cell vaccine as negative control. Data were shown as the mean ± SEM of triplicates.
Flow cytometric analysis of tumor tissue and peripheral blood from NOD/SCID mice with anti-hPSMA and anti-HLA. Tumor tissues and peripheral blood were isolated on the 30th and 60th day to prepare single cell suspensions. The presence of PSMA and HLA (human leukocyte antigen) was assessed with APC-labeled anti-hPSMA (1:100) and FITC-labeled anti-hHLA (1:200) monoclonal antibodies, respectively, for flow cytometric analysis. The LNCaP prostate cancer cells were used as a positive control because they could secrete PSA and express PSMA. (A) The single cell suspension from tumor tissue on day 30 with APC-labeled anti-hPSMA. (B) The LNCaP prostate cancer cells. (C) The single cell suspension from tumor tissue on day 30 with FITC-labeled anti-hHLA. (D) The blood from PC-3 inoculated NOD/SCID mice on day 30 with FITC-labeled anti-hHLA. (E) The white cells from PC-3 inoculated NOD/SCID mice on day 60 with FITC-labeled anti-hHLA.
Screen for the immune “leakage” phenomenon of NOD/SCID mice and detection of the levels of NK cells before and after injection of NK cell inhibitor GM1. (A) Concentration of IgG in peripheral blood serum of NOD/SCID mice. The immune “leakage” phenomenon was screened by the levels of IgG through ELISA kit (Beyotime) in 25 NOD/SCID mice with standard and blank controls (data from the controls not shown). The concentration of IgG lower than 10 μg/ml was defined as no immune leakage. (B) The changes of CD122 levels in peripheral blood of NOD/SCID mice before and after injection of NK cell inhibitor anti-asialo-GM1 antibody. CD122 was assessed with FITC-labeled anti-CD122 (1:200) monoclonal antibody for flow cytometric analysis. Left: CD122 level before injection of NK cell inhibitor anti-asialo-GM1 antibody; middle: CD122 level after injection of NK cell inhibitor anti-asialo-GM1 antibody; right: comparison of CD122 levels before and after injection of NK cell inhibitor anti-asialo-GM1 antibody.
Flow cytometric analysis of human lymphocytes in the peripheral blood and spleen tissue of huPBL-SCID mice after huPBL transplantation. (A) The presence of CD45+, CD8+, or CD4+ cells was assessed respectively with phycoerythrin (PE)-labeled anti-hCD45, PE-Cy7-labeled anti-hCD8, and PE-Cy7-labeled anti-hCD4 monoclonal antibodies for flow cytometric analyses. (B) Flow cytometric analysis of human CD45+ cells in the spleen tissue of huPBL-SCID mice 8 weeks after huPBL transplantation. Spleen was isolated from huPBL-SCID 8 weeks after huPBL transplantation and single cell suspensions were prepared from the isolated spleen. The presence of CD45+ cells was assessed with PE-labeled anti-hCD45 monoclonal antibody through a flow cytometer. NOD/SCID mice without huPBL transplantation were used as the negative controls.
Immunohistochemical staining of spleen and liver tissues from huPBL-SCID mice 8 weeks after huPBL transplantation. The images of immunohistochemical staining were shown with ×200 magnification. The spleen and liver tissues from huPBL-SCID mice were stained with anti-hCD4 or anti-hCD8 antibody (A), and the quantitative analysis of the images was performed with integrated optic density (B). The spleen and liver tissues from NOD/SCID mice without huPBL transplantation were used as negative controls.
Immunohistochemical staining analysis of the lymph node tissues from huPBL-SCID mice 8 weeks after vaccination. The images of immunohistochemical staining were shown with ×200 magnification. Lymph node tissues from different groups were stained with rat anti-hCD45 (A), anti-hCD4 (B), or anti-hCD8 antibody (C). The quantitative analysis of those images was carried out with integrated optic density (D).
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Lai, S., Huang, Z., Guo, Y. et al. Evaluation of hGM-CSF/hTNFα surface-modified prostate cancer therapeutic vaccine in the huPBL-SCID chimeric mouse model. J Hematol Oncol 8, 76 (2015). https://doi.org/10.1186/s13045-015-0175-8