Metronomic Chemotherapy Enhances Antitumor Effects of Cancer Vaccine by Depleting Regulatory T Lymphocytes and Inhibiting Tumor Angiogenesis

被引:74
作者
Chen, Chi-An [1 ]
Ho, Chih-Ming [2 ]
Chang, Ming-Cheng [1 ]
Sun, Wei-Zun [3 ]
Chen, Yu-Li [1 ]
Chiang, Ying-Cheng [1 ]
Syu, Ming-Hong [1 ]
Hsieh, Chang-Yao [1 ]
Cheng, Wen-Fang [1 ,4 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
[2] Cathay Gen Hosp, Dept Obstet & Gynecol, Gynecol Canc Ctr, Taipei, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Anesthesiol, Taipei, Taiwan
[4] Natl Taiwan Univ, Coll Med, Grad Inst Oncol, Taipei 10764, Taiwan
关键词
IMMUNOLOGICAL RESPONSES; PHASE-I; BREAST-CANCER; CELL VACCINE; IMMUNOTHERAPY; ANTIGEN; CYCLOPHOSPHAMIDE; MELANOMA; IMMUNITY; TRIAL;
D O I
10.1038/mt.2010.34
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Although cancer vaccines are emerging as innovative methods for cancer treatment, these alone have limited potential for treating measurable tumor burden. Thus, the importance of identifying anticancer strategies with greater potency is necessary. The chimeric DNA vaccine CTGF/E7 (connective tissue growth factor linked to the tumor antigen human papillomavirus 16 E7) generates potent E7-specific immunity and antitumor effects. We tested immune-modulating doses of chemotherapy in combination with the CTGF/E7 DNA vaccine to treat existing tumors in mice. Metronomic low doses of paclitaxel, not the maximal tolerable dose, are synergistic with the antigen-specific DNA vaccine. Paclitaxel, given in metronomic sequence with the CTGF/E7 DNA vaccine enhanced the vaccine's potential to delay tumor growth and decreased metastatic tumors in vivo better than the CTGF/E7 DNA vaccine alone. The two possible mechanisms of metronomic paclitaxel chemotherapy are the depletion of regulatory T cells and the inhibition of tumor angiogenesis rather than direct cancer cell cytolytic effects. Results indicate that combination treatment of metronomic chemotherapy and antigen-specific DNA vaccine can induce more potent antigen-specific immune responses and antitumor effects. This provides an immunologic basis for further testing in cancer patients.
引用
收藏
页码:1233 / 1243
页数:11
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