Dendritic Cell Immunotherapy Combined with Cytokine-Induced Killer Cells Effectively Suppresses Established Hepatocellular Carcinomas in Mice

被引:27
作者
Jung, Nam-Chul [1 ]
Lee, Jun-Ho [2 ]
Choi, Hyun-Ji [2 ]
Hwang, Sung-Uk [1 ]
Song, Jie-Young [3 ]
Seo, Han Geuk [4 ]
Choi, Jinjung [5 ]
Jung, Sang Youn [5 ]
Han, Sung Gu [6 ]
Lim, Dae-Seog [2 ]
机构
[1] Pharos Vaccine Inc, Songnam, Gyeonggi Do, South Korea
[2] CHA Univ, Dept Biotechnol, 335 Pangyo Ro, Songnam 463400, Gyeonggi Do, South Korea
[3] Korea Inst Radiol & Med Sci, Dept Radiat Canc Res, Seoul, South Korea
[4] Konkuk Univ, Dept Anim Biotechnol, Seoul, South Korea
[5] Bundang CHA Med Ctr, Dept Internal Med, Div Rheumatol, Songnam, Gyeonggi Do, South Korea
[6] Konkuk Univ, Coll Anim Biosci & Technol, Dept Food Sci & Biotechnol, Seoul, South Korea
关键词
Cytokine-induced killer cells; dendritic cells; hepatocellular carcinoma; T-CELLS; HEPATITIS-B; MELANOMA PATIENTS; CANCER; VACCINATION; INFECTION; ROLES; PROGRESSION; INDUCTION;
D O I
10.1080/08820139.2016.1183025
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: The response of hepatocellular carcinoma (HCC) to immunotherapy is often disappointing and new strategies are clearly needed. The aim of the present study was to investigate whether cytokine-induced killer (CIK) cells combined with a dendritic cell vaccination enhanced cytotoxicity against hepatocarcinoma tumor cells in an in vivo animal model.Methods: CIKs and DCs were prepared from C3H/HeJ mice by conventional methods, the dendritic cell (DC) pulsed with a MH134 cell lysate, DC or CIK alone were used as controls. Cell phenotypes were analyzed by flow cytometry, cytokine secretion levels were determined by enzyme-linked immunosorbent assay (ELISA), and cytotoxicity was assessed by means of an in vitro lactate dehydrogenase (LDH) release assay. A mouse hepatocarcinoma cell MH134-bearing mice model was established to test the in vivo anti-tumor efficacy of the system.Results: CIK cells combined with DC therapy resulted in significant inhibition of tumor growth compared with the control group, whereas the decrease in tumor growth in mice that had been treated with CIK or DC alone did not reach the level of statistical significance. The combination therapy led to a further increase in the population of cytotoxic T cells (CTLs) in vivo, compared to the CIK or DC alone therapy. In addition, the combination therapy significantly enhanced cytotoxic activity against MH134 cells.Conclusion: Taken together, these results show that a DC + CIK vaccination is more effective than DC or CIK alone therapy for the treatment of hepatocarcinoma cancer.
引用
收藏
页码:553 / 565
页数:13
相关论文
共 28 条
[1]   Induction of systemic CTL responses in melanoma patients by dendritic cell vaccination:: Cessation of CTL responses is associated with disease progression [J].
Andersen, MH ;
Keikavoussi, P ;
Bröcker, EB ;
Schuler-Thurner, B ;
Jonassen, M ;
Sondergaard, I ;
Straten, PT ;
Becker, JC ;
Kämpgen, E .
INTERNATIONAL JOURNAL OF CANCER, 2001, 94 (06) :820-824
[2]   Combination vaccine of dendritic cells (DCs) and T cells effectively suppressed preestablished malignant melanoma in mice [J].
Asada, Hidetsugu ;
Kishida, Tsunao ;
Hirai, Hideyo ;
Shin-Ya, Masaharu ;
Imanishi, Jiro ;
Takeuchi, Minoru ;
Mazda, Osam .
CANCER LETTERS, 2006, 240 (01) :83-93
[3]   Expansion of cytolytic CD8+ natural killer T cells with limited capacity for graft-versus-host disease induction due to interferon γ production [J].
Baker, J ;
Verneris, MR ;
Ito, M ;
Shizuru, JA ;
Negrin, RS .
BLOOD, 2001, 97 (10) :2923-2931
[4]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[5]   Dendritic cells and immunotherapy for cancer [J].
Chang, DH ;
Dhodapkar, MV .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2003, 77 (05) :439-443
[6]   Decreased numbers and impaired function of circulating dendritic cell subsets in patients with chronic hepatitis B infection (R2) [J].
Duan, XZ ;
Zhuang, H ;
Wang, M ;
Li, HW ;
Liu, JC ;
Wang, FS .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2005, 20 (02) :234-242
[7]   Hepatocellular carcinoma: Epidemiology and molecular carcinogenesis [J].
El-Serag, Hashem B. ;
Rudolph, Lenhard .
GASTROENTEROLOGY, 2007, 132 (07) :2557-2576
[8]   CURRENT CONCEPTS Hepatocellular Carcinoma [J].
El-Serag, Hashem B. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (12) :1118-1127
[9]   Ectopic expression of a T-box transcription factor, eomesodermin, renders CD4+ Th cells cytotoxic by activating both perforin- and FasL-pathways [J].
Eshima, Koji ;
Chiba, Sayuri ;
Suzuki, Harumi ;
Kokubo, Kenichi ;
Kobayashi, Hirosuke ;
Iizuka, Misao ;
Iwabuchi, Kazuya ;
Shinohara, Nobukata .
IMMUNOLOGY LETTERS, 2012, 144 (1-2) :7-15
[10]   Report of the 17th Nationwide Follow-up Survey of Primary Liver Cancer in Japan [J].
Ikai, Iwao ;
Arii, Shigeki ;
Okazaki, Masatoshi ;
Okita, Kiwamu ;
Omata, Masao ;
Kojiro, Masamichi ;
Takayasu, Kenichi ;
Nakanuma, Yasuni ;
Makuuchi, Masatoshi ;
Matsuyama, Yutaka ;
Monden, Morito ;
Kudo, Masatoshi .
HEPATOLOGY RESEARCH, 2007, 37 (09) :676-691