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新城鸡瘟病毒诱导小鼠腹腔巨噬细胞产生肿瘤坏死因子的细胞毒活性研究 被引量:1

CYTOTOXIC ACTIVITY OF TNF α
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摘要 目的观察新城鸡瘟病毒L系(NDV-L)诱导小鼠腹腔巨噬细胞(PEMΦ)产生的肿瘤坏死因子-α(TNF-α)对肿瘤细胞的细胞毒性作用。方法采用噻唑蓝(MTT)和3H-脱氧胸苷(3H-TdR)标记肿瘤细胞的方法。结果NDV-L可诱导小鼠PEMΦ产生TNF-α,其产生的量随NDV-L感染量的增加而活性增强。当NDV-L感染剂量一定时,TNF-α释放量在NDV-L作用PEMΦ24h时为最强(100U/ml)。用3H-TdR标记肿瘤细胞(小鼠乳腺癌细胞系Ca761-86和小鼠肥大细胞瘤P815)做TNF-α的细胞毒试验,表明其具有明显的杀伤活性。结论NDV-L诱导小鼠腹腔巨噬细胞产生的TNF-α具有明显的细胞毒活性。 PURPOSE To determine whether murine peritoneal elicited macrophage (PEMΦ) infected by Newcastle Disease Virus Losota Strain (NDV 1) could produce TNF α. METHODS MTT cotorimetic assay and labelling by 3H TdR for cytotoxic effect on tumor cells was used. RESULTS NDV 1 could induce TNF α (v mTNF α) from murine PEMΦ,and the quantity of the v mTNF α were interrelated to the infecting dose of NDV 1 and PEMΦ.When the NDV 1's dose was regular,the released quantities of the v mTNF α were highest at 24 hours.A significant cytotoxic activity of the v mTNF α to tumor cells (Ca 761 86 and P 815) labeled by 3H TdR was also found. CONCLUSIONS The TNF α produced from murine peritoneal elicited macrophage by NDV 1 had marked cytotoxicity.
出处 《中国癌症杂志》 CAS CSCD 1997年第3期203-205,共3页 China Oncology
基金 国家自然科学基金
关键词 巨噬细胞 肿瘤坏死因子 细胞毒 鸡新城疫病毒 Newcastle disease virus macrophages tumor necrosis factor
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  • 1蒋文军,卢绍平,魏阳,唐小兰,吴俊辉.新城鸡瘟病毒用于肿瘤特异性免疫治疗的研究进展[J].四川肿瘤防治,2003,16(1):60-61. 被引量:4
  • 2唐省三,马亚珍.新城疫病毒对体外培养人膀胱癌EJ细胞凋亡作用机制研究[J].陕西医学杂志,2005,34(5):521-524. 被引量:6
  • 3Kasuya H, Takeda S, Shimoyama S, et al. Oncolytic virus ther- apyforeword[J]. Curr Cancer Drug Targets, 2007,7(2) : 123-125.
  • 4Pardoll D. Therapeutic vaccination for cancer[J]. Clin lmmunol, 2000,95 (1) :s44-62.
  • 5Lee SO, Heo DS,Yoon SJ, et al. Effect of GM : CSF and II.-2 co-expression on the anti-tumor immune response[J]. Anticancer Res, 2000, 20(4):2681-2686.
  • 6Guha-Thakurta N, Majde JA. Early induction of proinflammato- ry cytokine and type I interferon mRNAs following Newcastle disease virus, poly]- rI : rC~, or low dose LPS challenge of the mouse[J]. J Interferon CytokineRes, 1997, 17 (4) :197.
  • 7Song E, Chen J, Antus B, et al. Interleukin-2 enhances suscep- tibility of colon cancer cells to FasR mediated apoptosis by up regulating Fas receptor level and down regulating FAP 1 expres sion[J]. Int J ImmunopatholPharmacol, 2000,13(3) : 113- 122.
  • 8Stanziale SF, Fong Y. Novel approaches to cancer therapy using oncolytic viruses[J]. Curr Mol Med, 2003,3 (1) : 61-71.
  • 9Janke M,Peeters B,Zhao H,et al. Activation of human T cells by a tumor vaccine infected with recombinant Newcastle diease virus producing IL-2[J]. Int J Oncol,2008,33(4) :823-832.
  • 10Zamarin D, Vigil A, Kelly K, et al. Genetically engineered New- castle diease virus for malignant melanoma therapy[J]. Gene T- her,2009,16(6) :796 804.

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