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单抗靶向超抗原SEA体内抗膀胱肿瘤实验研究

The anti-tumor effect of monoclonal antibody targeted superantigen SEA on human bladder cancer in vivo
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摘要 背景与目的:超抗原葡萄球菌肠毒素A(staphylococcal enterotoxin A,SEA)在体内、外以及临床的膀胱灌注治疗试验中对膀胱癌均具有明显的抑瘤效应,本研究旨在探讨单抗靶向的超抗原SEA体内对人膀胱癌的抑瘤作用。方法:以腹腔注射人外周血单个核细胞、皮下注射人膀胱癌BIU87细胞建立人免疫重建荷人膀胱癌SCID小鼠复合模型,再将模型小鼠随机分为对照组、SEA组及单抗靶向SEA实验组,分别予以PBS、SEA及单抗靶向SEA瘤周注射,以SonoSite彩超在建模后6周内检测小鼠皮下移植瘤体积、瘤体血流。结果:单抗靶向SEA组瘤体体积、瘤体血流均小于对照组及SEA组,在建模后4、5、6周差异均有统计学意义(P<0.05)。结论:单抗靶向的超抗原SEA对膀胱癌皮下移植瘤生长的抑制作用更强,可能与其进一步减少瘤体血流有关。 Background and purpose: Staphylococcal enterotoxin A (SEA) is potent T-cell stimulators which will produce significant tumor inhibition on bladder cancer. This study was to investigate the anti-tumor effect of monoclonal antibody targeted superantigen SEA on human bladder cancer in vivo. Methods: Hu-PBL-SCID mice of human bladder carcinoma, which were transplanted with human peripheral blood lymphocyte intraperitoneally and injected with human bladder carcinoma cells BIU87 subcutaneously, were divided randomly into 3 groups: control, SEA and monoclonal antibody targeted SEA group, subject to subcutaneous injection with PBS, SEA, or monoclonal antibody targeted SEA surrounding the xenografi respectively. Tumor size and blood flow were monitored under the SonoSite ultrasound system. Results: Compared with control and SEA groups, the tumor size and blood flow of monoclonal antibody targeted SEA group were significantly depressed (P〈0.05). Conclusion: Monoctonal antibody targeted SEA significantly depresses the xenograft growth, possibly through the down-regulation of tumor blood flow.
出处 《中国癌症杂志》 CAS CSCD 北大核心 2013年第1期32-35,共4页 China Oncology
基金 国家自然科学基金(No:81202007)
关键词 膀胱肿瘤 超抗原 葡萄球菌类毒素 抗体 单克隆 免疫治疗 Superantigens Staphylococcal enterotoxin A Antibodies monoclonal bladder carcinoma Immunotherapy
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参考文献14

  • 1MAINA E K,HU D L,TSUJI T. Staphylococcal enterotoxin A has potent superantigenic and emetic activities but not diarrheagenic activity[J].{H}International Journal of Medical Microbiology,2012,(02):88-95.
  • 2韩丛辉,郑宝钟,田军,季军捷,徐中华,侯怀水,崔先泉.超抗原诱导杀伤性T细胞体内外对膀胱肿瘤的杀伤作用研究[J].中华肿瘤杂志,2000,22(5):392-392. 被引量:14
  • 3FORSBERG G,SKARTVED N J,WALLéN-OHMAN M. Naptumomab estafenatox,an engineered antibody-superantigen fusion protein with low toxicity and reduced antigenicity[J].J Immunother,2010,(05):492-499.
  • 4ZHEN G,CONG-HUI H,LIN H. Preparation and in-vitro bioactivity of a novel superantigen conjugate targeting bladder carcinoma[J].{H}Journal of Pharmacy and Pharmacology,2009,(07):869-875.
  • 5HAN C,GONG Z,HAO L. Mechanism of monoclonal antibody-coupled staphylococcus superantigen-A induced apoptosis in human bladder cancer cells[J].{H}Cell Biochemistry and Biophysics,2011,(03):679-684.
  • 6GYORY F,MEZOSI E,SZAKALL S. Establishment of the hu-PBL-SCID mouse model for the investigation of thyroid cancer[J].{H}Experimental and Clinical Endocrinology and Diabetes,2005,(07):359-364.
  • 7SEITZ G,PFEIFFER M,FUCHS J. Establishment of a rhabdomyosarcoma xenograft model in human-adapted mice[J].{H}Oncology Reports,2010,(04):1067-1072.
  • 8贡震,韩从辉.浅表性膀胱癌的灌注治疗[J].中华泌尿外科杂志,2009,30(10):717-719. 被引量:4
  • 9MUNDI?ANO J,BERGUER P M,CABRERA G. Superantigens increase the survival of mice bearing T cell lymphomas by inducing apoptosis of neoplastic cells[J].PLoS One,2010,(12):e15694.
  • 10PERABO F G,WILLERT P L,WIRGER A. Superantigen-activated mononuclear cells induce apoptosis in transitional cell carcinoma[J].{H}Anticancer Research,2005,(05):3565-3573.

二级参考文献24

  • 1赵翀,俞莉章,张春丽,谢蜀生,潘中云,顾方六.抗人膀胱癌单克隆抗体及其偶联物靶细胞结合特性的免疫…[J].中华泌尿外科杂志,1993,14(5):330-332. 被引量:3
  • 2叶炯贤,潘雪娜,贾少微,高凤彤,李翀.抗人膀胱癌单克隆抗体BDI-1的扩增和鉴定[J].中华实验外科杂志,2006,23(6):742-743. 被引量:1
  • 3Witjes JA, Hendricksen K. lntravesical pharmacotherapy for non muscle invasive bladder cancer: a critical analysis of currently available drugs, treatment schedules, and long term results. Eur Urol, 2008, 53:45- 52.
  • 4Campodonico F, Mattioli F, Manfredi V, et al. Pharmacokinetics and toxicity of an early single intravesical instil lation of gemcitabine after endoscopic resection of superficial bladder cancer. Anticancer Res, 2007, 27: 1179-1183,.
  • 5Smith EB, Schwartz M, Kawamoto H, et al. Antitumor effects of imidazoquinolines in urothdial cell carcinoma of the bladder. J Urol, 2007, 177: 2347-2351.
  • 6Hendrieksen K, Wltjes JA. Current strategies for first and second line intravesieal therapy for nonmusele invasive bladder cancer. Curr Opin Urol, 2007, 17: 352-357.
  • 7Bartoletti R, Cai T, Gacci M, et al. Intravesical gemcitabine therapy for superficial transitional cell careinoma:results of a Phase II prospective multi center study. Urology, 2005, 66: 726-731.
  • 8Dalbagni G, Russo P, Bochner B, et al. Phase II trial of intravesical gemcitabine in bacille Calmette-Gueriwrefractory transitional cell carcinoma of the bladder. J Clin Oncol, 2006, 24: 2729 -2734.
  • 9van der Heijden AG, Moonen PM, Cornel EB, et al. Phase II marker lesion study with intravesicaI instillation of apaziquone for superficial bladder cancer:toxicity and marker response. J Urol, 2006, 176: 1349-1353.
  • 10McKiernan JM, Masson P, Murphy AM et al. Phase I trial of intravesical do cctaxel in the management of superficial bladder cancer refractory to stand ard intravesical therapy. J Clin Oncol 2006, 24: 3075-3080.

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