Table 1.
Recent studies of DC vaccine in HCC and PDAC treatment
| Year | Tumor model | Cancer type | DC load method | Conclusion | Ref. |
|---|---|---|---|---|---|
| 2013 | Humanized immune reconstituted HepG2 HCC murine model | HCC | DRibbles-pulsed dendritic cell | DRibbles-pulsed DC immunization induced a specific T cell response against HCC and resulted in significant inhibition of tumor growth compared to mice treated with DCs alone. | [55] |
| 2013 | Orthotopic pancreatic tumors | PDAC | Non-loaded Bone marrow-derived DC | DC vaccination followed by Gem treatment led to a significant delay in tumor growth and improved survival in pancreatic cancer-bearing mice. | [85] |
| 2014 | Subcutaneous or orthotopic pancreatic tumors | PDAC | Bone marrow-derived DC were loaded with soluble OVA protein | Gemcitabine enhances therapeutic efficacy of DC vaccination despite its negative influence on vaccine-induced T-cell proliferation. | [84] |
| 2014 | Xenograft model using immunodeficient mice | PDAC | Baculovirus (BV)-infected dendritic cells (DCs) | After treatment with BV-infected bone marrow-derived dendritic cells (BMDCs), human pancreatic tumors caused by AsPC-1 cells in a nude mouse model were significantly reduced in size, and the survival of the mice was improved compared with that of non-immature BMDC (iDC)- and BV-DC-immunized mice. | [87] |
| 2016 | MH134-bearing mice model | HCC | DC pulsed with a MH134 cell lysate | DC + CIK vaccination is more effective than DC or CIK alone therapy for the treatment of hepatocarcinoma cancer. | [89] |
| 2016 | Orthotopic murine HCC model | HCC | DC pulsed with a Hepa1-6 cell lysate | 90 % survival rate by day 60 compared with a survival rate lower than 5 % for untreated mice. | [79] |
| 2016 | Nude mice co-injected with MHCC97 cells and Hepa 1-6 induced tumor-bearing C57/BL6 immune competent mice | HCC | SP cell lysate-pulsed DCs | DCs loaded with SP cell lysates could induce a T cell response in vivo and suppress the tumor growth. | [90] |