Activation of antitumor immune responses by Ganoderma formosanum polysaccharides in tumor-bearing mice

被引:37
作者
Wang, Cheng-Li [1 ]
Lu, Chiu-Ying [1 ]
Hsueh, Ying-Chao [1 ]
Liu, Wen-Hsiung [1 ]
Chen, Chun-Jen [1 ]
机构
[1] Natl Taiwan Univ, Dept Biochem Sci & Technol, Taipei 10617, Taiwan
关键词
Ganoderma formosanum; Polysaccharides; Immunomodulation; Antitumor; T-CELL RESPONSES; LUCIDUM POLYSACCHARIDES; DENDRITIC CELLS; BETA-GLUCAN; CANCER; THERAPY; INNATE; RECOGNITION; LYMPHOCYTES; ANTICANCER;
D O I
10.1007/s00253-014-6027-6
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 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Fungi of the genus Ganoderma are basidiomycetes that have been used as traditional medicine in Asia and have been shown to exhibit various pharmacological activities. We recently found that PS-F2, a polysaccharide fraction purified from the submerged culture broth of Ganoderma formosanum, stimulates the maturation of dendritic cells and primes a T helper 1 (Th1)-polarized adaptive immune response in vivo. In this study, we investigated whether the immune adjuvant function of PS-F2 can stimulate antitumor immune responses in tumor-bearing mice. Continuous intraperitoneal or oral administration of PS-F2 effectively suppressed the growth of colon 26 (C26) adenocarcinoma, B16 melanoma, and sarcoma 180 (S180) tumor cells in mice without adverse effects on the animals' health. PS-F2 did not cause direct cytotoxicity on tumor cells, and it lost the antitumor effect in mice with severe combined immunodeficiency (SCID). CD4(+) T cells, CD8(+) T cells, and serum from PS-F2-treated tumor-bearing mice all exhibited antitumor activities when adoptively transferred to na < ve animals, indicating that PS-F2 treatment stimulates tumor-specific cellular and humoral immune responses. These data demonstrate that continuous administration of G. formosanum polysaccharide PS-F2 can activate host immune responses against ongoing tumor growth, suggesting that PS-F2 can potentially be developed into a preventive/therapeutic agent for cancer immunotherapy.
引用
收藏
页码:9389 / 9398
页数:10
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