2012
DOI: 10.1007/s00432-012-1298-8
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Immunotherapy by autologous dendritic cell vaccine in patients with advanced HCC

Abstract: Background Dendritic cells (DCs) could be used as potential cellular adjuvant for the production of specific tumor vaccines. Objectives Our study was aimed to evaluate the safety and efficacy of autologous pulsed DC vaccine in advanced hepatocellular carcinoma (HCC) patients in comparison with supportive treatment. Methods Thirty patients with advanced HCC not suitable for radical or loco-regional therapies were enrolled. Patients were divided into 2 groups, group I consisted of 15 patients received I.D va… Show more

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Cited by 88 publications
(63 citation statements)
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“…Moreover, chronic infection, necrosis and cell regeneration, fibrosis and cirrhosis are, together with the direct mechanisms, the high risk factors for HCC. Finally, HBV or HCV chronic infection has immunomodulatory and immunosuppressive effects [71][72][73] .…”
Section: Development Of Hcc In Chronic Hcv Infectionmentioning
confidence: 99%
“…Moreover, chronic infection, necrosis and cell regeneration, fibrosis and cirrhosis are, together with the direct mechanisms, the high risk factors for HCC. Finally, HBV or HCV chronic infection has immunomodulatory and immunosuppressive effects [71][72][73] .…”
Section: Development Of Hcc In Chronic Hcv Infectionmentioning
confidence: 99%
“…In the present study, HepG2 cells were used for T cell cytotoxicity analysis. Although the HepG2 cell line has been demonstrated to be misidentified and be derived from hepatoblastoma instead of hepatocellular carcinoma (25), the use of HepG2 cells as a model of target cells derived from tumor tissues is suitable for cytotoxicity analysis of immune cells cultured in vitro (26)(27)(28). Among the four groups (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…Notably, a monthly boost vaccination resulted in a significantly better 1 year survival [74] . In another RCT on advanced HCC, DCs pulsed with HepG2 cell lysate resulted in 13.3% patients with PR and 60% with SD after 6 mo of treatment [75] . However, the proportion of clinical response with this therapy is relatively low.…”
Section: Tumor Vaccine Using Antigen-presenting Cellsmentioning
confidence: 97%