Dendritic cells |
immunotherapy |
The combination of DC vaccine and PD-L1 inhibitor resulted in longer overall survival, smaller tumor size, and higher tumor cell apoptosis rate in mice. The combination of DC vaccine and PD-L1 inhibitor may have broad prospects as a new therapeutic strategy for HCC. |
Teng et al. (2020)
|
Dendritic cells |
The immune mechanism |
XCL1-GPC3 cells chemically attract murine XCR1CD8α dendritic cells (DCs) and human XCR1CD141 DCs, and promote their IL12 production. |
Chen et al. (2020)
|
Dendritic cells |
The immune mechanism |
A more severe reduction in basal OCR was observed in tumor-derived DCs exposed to AFP due to down-regulation of cytochrome C oxidase. The expression of PGC1-α in circulating medullary DC in HCC patients was decreased, and the ability to stimulate the function of antigen-specific effector was impaired, indicating the negative effect of AFP on DC metabolism. |
Santos et al. (2019)
|
Dendritic cells |
The immune mechanism |
AFP down-regulated CD1 on DC, but had little effect on NKT cell activation. |
Li et al. (2019a)
|
Dendritic cells |
The immune mechanism |
DC-CIK cells can inhibit the growth of HCC and LCSC in vitro and in vivo, and the most successful DC-triggered cell killing activity can be achieved through their LCSC antigen loading. |
Yang et al. (2018b)
|
Dendritic cells |
The immune mechanism |
MIP-10 enhances the antitumor activity of the DC/tumor fusion vaccine by alleviating the immunosuppressive tumor environment. |
Hu et al. (2017)
|
Dendritic cells |
immunotherapy |
The use of nifurazine and DC-loaded TCL significantly increased the survival rate, inhibited tumor growth and promoted anti-tumor immune response in HCC mice implanted in situ. |
Zhao et al. (2017b)
|
Dendritic cells |
immunotherapy |
Overexpression of IL-12 induced by adenovirus vector can effectively immunize DC. Intratumor but not systemic injection of activated IL-12-DC is essential for effective tumor regression. Improved immunotherapy with IL-12-DC represents a promising approach for the treatment of HCC. |
Vogt et al. (2014)
|
Dendritic cells |
immunotherapy |
β-GC activated mouse liver NKT cells and enhanced the anti-tumor activity of PAD-HBsAg-DC. β-GC may act as an effective innate immune enhancer to enhance the antitumor effect of PAD-HBsAg-DC vaccine. |
Long et al. (2013)
|
Dendritic cells |
immunotherapy |
Camory may play an important role in the development and progression of HCC through recruitment of DC and NK cells. |
Lin et al. (2011)
|
Dendritic cells |
The immune mechanism |
Electroporation of GPC-3 mRNA is an effective method for antigen-carrying monocytes to generate DCs because they produce functional GPC-3 reactive T cells in vitro.
|
O'Beirne et al. (2010)
|
Dendritic cells |
The immune mechanism |
Immature DCs(IMDCs) derived from human monocytes were fully mature after effective phagocytosis of dying cells, and showed significant proliferation and cytotoxicity to HLA-matched HEPG (2) cells in autologous peripheral blood monocytes (PBMC). |
Xing et al. (2009)
|
Dendritic cells |
The immune mechanism |
Secondary lymphoid tissue chemokines (SLC) are strongly expressed in secondary lymphoid organs. It has the ability to promote dendritic cell (DC) and T cell chemotaxis, making it a promising candidate for cancer therapy. |
Liang et al. (2007)
|
Dendritic cells |
immunotherapy |
AdvHAFP-transduced DCs activate higher frequencies of Th1 CD4 responses to AFP in healthy donors and AFP positive HCC patients. Importantly, when activated by adenovirus-engineered DC, the cytokine expression profile of CD4+T cells was biased towards the production of interleukin-2 and interferon-γ, which has therapeutic implications for vaccination work. |
Evdokimova et al. (2007)
|
Dendritic cells |
immunotherapy |
Dendritic cells transfected with total HCC mRNA stimulated an antigen-specific cytotoxic T cell response capable of recognizing and killing autologous tumor cells in vitro. |
Peng et al. (2006)
|
Dendritic cells |
The immune mechanism |
Impairment of MDCs produced by IL-12 may result in impaired stimulation of naive T cells, suggesting that targeted IL-12 therapy may enhance tumor-specific immune responses in patients with HCC. |
Ormandy et al. (2006)
|
Dendritic cells |
immunotherapy |
The combination of PEI or RFTA with active antigen-specific immunotherapy using DCS is a promising approach to induce a sustained anti-tumor immune response aimed at reducing tumor recurrence and metastasis in patients with HCC. |
Ali et al. (2005)
|
Dendritic cells |
The immune mechanism |
The phenotypic and functional deficits of PBMC-derived DCs in LC and HCC patients may play a key role in HBV infection and HCC immune escape. After tumor is stimulated by antigen, DC function can be enhanced in LC patients. |
Wong et al. (2005)
|
Dendritic cells |
The immune mechanism |
Ad-HBsAg-transduced DCs stimulated a strong cytotoxic T lymphocyte (CTL) response to HBsAg-expressing tumor cells and protected mice from lethal tumor attack. |
Qiu et al. (2005)
|
Dendritic cells |
immunotherapy |
At concentrations up to 20 μg/mL, AFP did not alter the in vitro generation, maturation and T cell stimulation of DC. Higher AFP concentration ( >20 μg/ml) led to phenotypic changes in DC without impair its ability to stimulate CD4+ T cells. Independent of serum AFP levels, the frequency and function of DC and AFP-specific T cells did not decrease in HCC patients. |
Ritter et al. (2004)
|
Dendritic cells |
immunotherapy |
Autologous DCs containing the HCA587 protein can induce specific T cell responses in healthy individuals by in vitro stimulation, and HCA587 is a good candidate for the development of a protein-based therapeutic DC tumor vaccine for the treatment of HCC patients. |
Li et al. (2004)
|
Dendritic cells |
immunotherapy |
DCs transfected with MAGE-1 gene can induce higher cytotoxicity of SMMC7721 in vitro, suggesting that this transgenic DC may have the potential to induce specific antitumor activity and be used as a novel HCC vaccine. |
Liu et al. (2001)
|
Dendritic cells |
The immune mechanism |
Decline in DC function and normal T cell response were observed in HBV-infected HCC patients, suggesting that the low function of DC is related to the pathogenesis of HBV or HCV-infected HCC. |
Kakumu et al. (2000)
|