PMID- 16911943 OWN - NLM STAT- MEDLINE DCOM- 20061219 LR - 20141120 IS - 1499-3872 (Print) VI - 5 IP - 3 DP - 2006 Aug TI - Effects of cytotoxic T lymphocytes on hepatoma cell line SMMC-7721 induced by different subsets of dendritic cells in vitro. PG - 422-7 AB - BACKGROUND: Dendritic cells (DCs) loaded with complex antigen are always used to induce cytotoxic T lymphocytes (CTLs) which have a specific anti-tumor activity. However, CTLs can assault autologous cells induced by DCs loaded with autologous antigen. This study aimed to explore how to weaken the autoimmune reaction induced by DC vaccine by combining mature DC (mDC) activating immunity and immature DC (imDC) leading to immune tolerance to make hepatocellular carcinoma (HCC) vaccine in vitro. METHODS: DC progenitors derived from human peripheral blood were assigned to two groups. One was cultured to mDC and pulsed with frozen-thawed antigen (FTA) of human HCC cell line SMMC-7721 cells (mDC group), and the other was cultured to imDC and pulsed with FTA of human liver cell line L-02 cells (imDC group). The morphology of DCs was monitored and cells phenotypes including HLA-DR, CD80, CD1alpha, CD83 were assayed by flowcytometry (FCM). The concentrations of interleukin-12 (IL-12) in the supernatant were assayed by ELISA. Methyl thiazolyl tetrazolium (MTT) was used to evaluate T cell proliferation induced by mDC and imDC and the killing rate of CTL induced by mDC and imDC respectively/together on SMMC-7721 and L-02 cells. RESULTS: Compared with the imDC group, the mDC group was characterized by the following: increased secretion of IL-12 (P<0.05); higher expression of HLA-DR, CD1alpha, CD80, CD83; and stronger activity in stimulating proliferation of isogenic T cells (P<0.05). CTL induced by the mDC group had a significant killing response to SMMC-7721 as well as a higher killing rate for L-02 (P>0.05). CTL induced by mDC and imDC together had a higher killing response to SMMC-7721, but a lower killing rate for L-02 (P<0.01). CONCLUSIONS: CTL induced by mDC and imDC together has a higher antigen-specific killing response in vitro than that induced by mDC alone. This may be of greater clinical value. FAU - Wang, Jia-Xiang AU - Wang JX AD - Department of Surgery, First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China. wjiaxiang@zzu.edu.cn FAU - Liu, Guang-Hui AU - Liu GH FAU - Fan, Ying-Zhong AU - Fan YZ FAU - Liu, Qiu-Liang AU - Liu QL FAU - Zhou, Juan AU - Zhou J FAU - Zhang, Dong-Yun AU - Zhang DY FAU - Qi, Yuan-Ming AU - Qi YM LA - eng PT - Journal Article PL - Singapore TA - Hepatobiliary Pancreat Dis Int JT - Hepatobiliary & pancreatic diseases international : HBPD INT JID - 101151457 SB - IM MH - Carcinoma, Hepatocellular/*immunology MH - Cell Line, Tumor MH - Dendritic Cells/*immunology MH - Enzyme-Linked Immunosorbent Assay MH - Flow Cytometry MH - Humans MH - In Vitro Techniques MH - T-Lymphocytes, Cytotoxic/*immunology EDAT- 2006/08/17 09:00 MHDA- 2006/12/21 09:00 CRDT- 2006/08/17 09:00 PHST- 2006/08/17 09:00 [pubmed] PHST- 2006/12/21 09:00 [medline] PHST- 2006/08/17 09:00 [entrez] AID - 868 [pii] PST - ppublish SO - Hepatobiliary Pancreat Dis Int. 2006 Aug;5(3):422-7.