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Effects of anticancer agents on cell viability,proliferative activity and cytokine production of peripheral blood mononuclear cells
Authors:Hiromi Sakai  Satoshi Kokura  Takeshi Ishikawa  Reiko Tsuchiya  Manabu Okajima  Tatsuzou Matsuyama  Satoko Adachi  Kazuhiro Katada  Kazuhiro Kamada  Kazuhiko Uchiyama  Osamu Handa  Tomohisa Takagi  Nobuaki Yagi  Yuji Naito  Toshikazu Yoshikawa
Affiliation:1Department of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto 602-8566, Japan;2Department of Cancer ImmunoCell Regulation, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto 602-8566, Japan
Abstract:We investigated the effects of anticancer agents on peripheral blood mononuclear cells for the purpose of providing data to support new translational chemoimmunotherapy regimens. Peripheral-blood mononuclear cells were treated with one of four anticancer agents (5-fluorouracil, irinotecan, cisplatin, and gemcitabine) for 2 h, after which cell viability was determined. For assessment of effects of each drug on proliferation and cytokine production, cells were stimulated with phytohemagglutinin for 48 h. As a result, the anticancer agents did not affect cell viability. Cell proliferation was unaffected by 5-fluorouracil and irinotecan but inhibited by cisplatin and gemcitabine. Treatment with gemcitabine enhanced the production of IFN-γ and decreased the number of regulatory T cells. gemcitabine treatment increased IFN-γ production among CD4 T cells but not among CD8 T cells. The results indicated that GEM had immunoregulatory properties that might support immune response against cancer. This finding has implications for designing chemoimmunotherapy strategies.
Keywords:chemoimmunotherapy  5-fluorouracil (5-FU)  irinotecan (CPT-11)  cisplatin (CDDP)  gemcitabine (GEM)
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