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成纤维细胞介导白细胞介素6基因疗法对化疗导致的造血损伤的恢复作用 被引量:6

FIBROBLAST-MEDIATED HUMAN INTERLEUKIN-6 GENE THE-RAPY ACCELERATES THE RECOVERY OF CHEMOTHERAPY-INDUCED HEMATOIETIC SUPRESSION
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摘要 研究了成纤维细胞介导的人白细胞介素6(Intetrleukin-6,IL-6)基因疗法对预先体内注射150mg/kg5-氟尿嘧啶(5-FU)所造成的造血损伤小鼠模型的治疗作用。结果发现,外周血血小板数量在移殖高分泌IL-6成纤维细胞后第10天开始持续上升,第22天血小板数量恢复到化疗前水平,中性粒细胞数量也显著增高,但对白细胞恢复没有明显的促进作用。骨髓和脾脏CFU-GM及CFU-MK在体内移殖高分泌IL-6成纤维细胞后,体外动态观察发现:骨髓和脾脏CFU-GM、CFU-MK在第4~7天左右数量为0,在第10天左右数量开始上升,于第16天左右数量显著增高,对CFU-GM、CFU-MK具有明显的恢复作用,CFU-S数量也显著增高。表明成纤维细胞介导的白细胞介素6基因疗法能显著治疗化疗导致的造血损伤,可望为肿瘤放、化疗导致的机体造血损伤提供新的治疗途径。 n the present study , we examined the effect of fibroblast mediated human interleukin-6(IL-6) gene therapy on the mice that have been injected intraperitoneally 5-fluorouracil(5-FU)at a dose of 150mg/kg. We observed that the number of plateletes in peripheral blood increasedat day 10 after implantation of IL-6 highly-secreting fibroblast cells and returned to normal atday 22. Neutrophil counts were also elevated , but WBCs were not accelerated to recover fromchemotherapy. In the colony formation, CFU-GM、CFU-MK in bone marrow and spleen was notfound at day 4~7 after implantation of IL-6 highly-secreting fibroblast cells. The numbers ofCFU-GM. CFU-MK were enhanced after day 10 and had a significant increase after day 16.CFU-GM、CFU-MK in bone marrow and spleen were accelerated to recover. CFU-S was alsomarkedly argumented in mice. These data demonstrated that fibroblast-mediated human IL-6gene therapy can treat chemotherapy-induced hematopoietic suppression effectively. The experi-ment outlines a new approach to treat chemotherapy or radiotherapyinduced hematopoietic sup-pression.
出处 《中国免疫学杂志》 CSCD 北大核心 1995年第3期153-157,共5页 Chinese Journal of Immunology
基金 国家自然科学基金和军队八五攻关基金
关键词 白细胞介素6 基因治疗 成纤维细胞 药物疗法 interleukin6 Gene therapy Fibroblast ChemotherapyHematopoietic recovery
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