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成纤维细胞介导的人α5型干扰素基因治疗白血病的实验研究 被引量:3

EXPERIMENTAL STUDY ON THE TREATMENT OF LEUKEMIA BY FIBROBLAST-MEDIATED HUMAN INTERFERON-αGENETHERAPY
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摘要 人白血病细胞HL-60在体外经NIH3T3-IFN-α ̄+细胞培养上清作用后或与该细胞共育后其生长受到显著抑制,细胞形态出现空泡,核固缩等现象。给裸鼠皮下接种HL60细胞(1×10 ̄7/只),当皮下肿瘤结节长至5mm时,给荷瘤小鼠腹腔内埋植1×10 ̄7NIH3T3-IFN-α ̄+细胞或腹腔注射阿霉素,结果发现,其皮下肿瘤结节的生长受到非常显著的抑制,特别是当NIH3T3-IFN-α ̄+细胞与阿霉素联合应用时,肿瘤生长抑制作用最明显。表明成纤维细胞介导的人IFN-α5基因疗法对人白血病有一定的治疗效果,当与适当化疗药物联合应用时疗效更佳。 ecause hIFN-αis very effective in treating patients with leukemia,we investigated the effect of fibroblast-mediated hlFN-αgene therapy on the human leukemia-bearing nude mice. Thegrowth of human HL-60 leukemia cells were inhibited significantly after HL-60 cells were incu-bated with the NIH3T3-IFN-α ̄+ cells or their ctilture stipernatants.The HL-60 cells were inocu-lated sc into nLide mice, and then the NIH3T3- IFN- α ̄+cells were implaiited ip iiito the leukemi-a-bearing mice or Dox was also injected ip into the leukemia-bearing mice, The results demonstrated that the in vivo growth of the leukemia cells was inhibited obviously,and the better ther-apeutic effect could be achived when NIH3T3-IFN-α ̄+cells were used in combination with Dox。suggesting that the fibroblast mediated human IFN-α gene therapy could be used to treat humanleukemia effectively and the therapeutic effect would be better when it is used with chemothera-py。
出处 《中国免疫学杂志》 CAS CSCD 北大核心 1995年第4期239-243,共5页 Chinese Journal of Immunology
基金 国家自然科学基金 军队八五攻关基金
关键词 干扰素 基因治疗 成纤维细胞 白血病 阿霉素 Human interferon-αGene therapy Fibroblast cells Leukemia Adriamycin Chemoimmunotherapy
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