Effect of levamisole (NSC-177023) on DNA synthesis by lymphocytes from immunosuppressed C57BL mice.

Cancer chemotherapy reports Pub Date : 1975-05-01
W A Woods, M J Filegelman, M A Chirigos
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Abstract

The effect of in vivo treatment of C57BL mice with BCNU and/or levamisole on the in vitro DNA synthetic capacity of their spleen cells was studied as a measure of cell-mediated immune function. BCNU treatment was suppressive to spleen cell DNA synthesis; conversely, treatment with levamisole was stimulatory. Levamisole treatment 5-8 days after BCNU treatment resulted in significant recovery of DNA synthetic capacity. Multiple doses of levamisole were not more effective than single doses. Allogeneic stimulation of BCNU-suppressed lymphocytes was not consistently increased by levamisole treatment.

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左旋咪唑(NSC-177023)对免疫抑制小鼠淋巴细胞DNA合成的影响。
研究了BCNU和/或左旋咪唑对C57BL小鼠脾细胞体外DNA合成能力的影响,以此作为细胞介导免疫功能的指标。BCNU对脾细胞DNA合成有抑制作用;相反,左旋咪唑治疗是刺激性的。BCNU治疗后5-8天左旋咪唑治疗可显著恢复DNA合成能力。多剂量左旋咪唑并不比单剂量更有效。左旋咪唑治疗不一致地增加bcnu抑制淋巴细胞的异体刺激。
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PORFIROMYCIN. Phase I study of 5-azacytidine (NSC-102816) using 24-hour continuous infusion for 5 days. Bleomycin (NSC-125066) and CCNU (NSC-79037) in the combination chemotherapy of mopp-resistant hodgkin's disease. Combination chemotherapy with 5-fluorouracil (NSC-19893), methotrexate (NSC-740), and prednisolone (NSC-9900) (FAP protocol) for hepatoma. Cyclophosphamide (NSC-26271) maintenance therapy after a second remission of childhood acute lymphoblastic leukemia: comparative clinical trial (standard dose versus intermittent high dose versus cyclophosphamide plus cytosine arabinoside (NSC-63878)).
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