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新型重组免疫毒素DT390-mRantes治疗小鼠EAE的初步研究 被引量:2

Primary study of the recombinant immunotoxin DT390-mRantes in EAE therapy
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摘要 目的:构建一种含有重组免疫毒素DT390-mRantes(白喉杆菌外毒素390片段-活化T细胞表达与分泌调节因子)的真核表达质粒,并用于治疗小鼠实验性自身免疫性脑脊髓炎(EAE)。方法:利用自提的MBP诱导C57BL/6小鼠产生EAE,将mRantes导入含有DT390的真核表达质粒SRα中,经阳离子纳米脂质体包被后,治疗小鼠EAE,同时对其临床症状、脑部病理改变、外周血相关细胞因子及T/B细胞比例进行检测,了解该重组免疫毒素的治疗效果。结果:成功构建真核表达质粒DT390-mRantes-SRα,治疗组小鼠临床症状减轻,脑部特异性淋巴细胞浸润减少,外周T细胞相关细胞因子表达降低,T/B细胞比例降低。结论:新型重组免疫毒素DT390-mRantes治疗小鼠EAE有较为明显的效果,为治疗人的多发性硬化(MS)提供有益的借鉴。 AIM: To construct a novel eukaryotic expression plasmid including the recombinant immunotoxin DT390-mRantes and treat experimental autoimmune encephalomyelitis (EAE) in mice. METHODS. EAE in C57BL/6 mice were induced by the extracted MBP. The mRantes fragment was inserted into the eukaryotic expression plasmid SRα containing DT390. Then cationic liposome-embedded plasmid DNA was injected into the muscles of the hind-limbs in mice. The effect of DT390-mRantes was evaluated by observing clinical symptoms, pathological changes of brain, relative cytokine of peripheral blood, and the proportion of T cells and B cells. RESULTS: The recombinant immunotoxin DT390-mRantes was successfully constructed. Compared the mice in treated group with those in untreated group the clinical symptoms of EAE were allevi- ated, the infiltration of inflammatory cells were decreased, the IFN-y level was fallen, and the ratio of T/B cells was decreased. CONCLUSION: The recombinant immunotoxin DT390-mRantes has distinct effects on EAE in mice, which may be used for beneficial reference to the therapy of MS.
出处 《细胞与分子免疫学杂志》 CAS CSCD 北大核心 2007年第3期236-239,共4页 Chinese Journal of Cellular and Molecular Immunology
基金 国家高技术研究发展计划(863)资助项目(2002AA214101) 国家自然基金委创新研究群体基金项目(30221001) 四川省应用基础项目资助(04JY029-002)
关键词 实验性变态性脑脊髓炎 DT390 mRantes 重组免疫毒素 experimental autoimmune encephalomyelitis (EAE) DT390 mRantes recombinant imunotoxin
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参考文献11

  • 1Petry K,Boulleme A,Pousset F,et al.Experimental allergic encephalomyelitis animal models for analyzing features of multiple sclerosis[J].Pathol Biol,2000,48(1):47-53.
  • 2Mekala DJ,Alli RS,Geiger TL.IL-10-dependent suppression of experimental allergic encephalomyelitis by Th2-differentiated,anti-TCR redirected T lymphocytes[J].J Immunol,2005,174(6):3789-3797.
  • 3Luca ME,Kel JM,van Rijs W,et al.Mannosylated PLP(139-151) induces peptide-specific tolerance to experimental autoimmune encephalomyelitis[J].J Neuroimmunol,2005,160(1-2):178-187.
  • 4Smith PA,Morris-Downes M,Heijmans N,et al.Epitope spread is not critical for the relapse and progression of MOG 8-21 induced EAE in Biozzi ABH mice[J].J Neuroimmunol,2005,164(1-2):76-84.
  • 5Karlsson I,Antonsson L,Shi Y,et al.Coevolution of RANTES sensitivity and mode of CCR5 receptor use by human immunodeficiency virus type 1 of the R5 phenotype[J].J Virol,2004,78(21):11807-11815.
  • 6Deibler GE,Martenson RE,Kies MW.Large scale preparation of myelin basic protein from central nervous system tissue of several mammalian species[J].Prep Biochem,1972,2(2):139-165.
  • 7孙逊,张志荣.脂质-鱼精蛋白-DNA复合物的构建及其对细胞的体外转染[J].药学学报,2004,39(10):792-796. 被引量:6
  • 8Kono DH,Urban JL,Horvath SJ,et al.Two minor determinants of myelin basic protein induce EAE in SJL/J mice[J].J Exp Med,1988,168(1):213-227.
  • 9沈柱,刘玉峰,王刚.以T细胞介导为主的自身免疫性疾病的干预策略[J].细胞与分子免疫学杂志,2005,21(B03):71-73. 被引量:6
  • 10Fife BT,Paniagua MC,Lukacs NW,et al.Chemokine receptor expression by central nervous system-infiltrating encephalitogenic T cells during experimental autoimmune encephalomyelitis[J].J Neurosci Res,2001,66(4):705-714.

二级参考文献16

  • 1Masteller EL, Warner MR, Ferlin W, et al. Peptide-MHC class II dimers as therapeutics to modulate antigen-specific T cell responses in autoimmune diabetes[J]. J Immunol, 2003, 171(10): 5587-5595.
  • 2Szodoray P, Jellestad S, Nakken B, et al. Programmed cell death in rheumatoid arthritis peripheral blood T-cell subpopulations determined by laser scanning cytometry[J]. Lab Invest, 2003, 83(12): 1839-1848.
  • 3Cappellesso S, Thibault G, Hoarau C, et al. FasL-transfected endothelial cells decrease the proliferative response of allogeneic PBL[J]. Transpl Immunol, 2002, 10(4): 293-302.
  • 4Anderson CF, Lucas M, Gutierrez-Kobeh L, et al. T cell biasing by activated dendritic cells[J]. J Immunol, 2004, 173(2): 955-961.
  • 5Cameron AL, Kirby B, Fei W, et al. Natural killer and natural killer-T cells in psoriasis[J]. Arch Dermatol Res, 2002, 294(8): 363-369.
  • 6Rudolph MG, Wilson IA. The specificity of TCR/pMHC interaction[J]. Curr Opin Immunol, 2002, 14(1): 52-65.
  • 7Achiron A, Mandel M. T-cell vaccination in multiple sclerosis[J]. Autoimmun Rev, 2004, 3(1): 25-32.
  • 8Direskeneli H, Eksioglu-Demiralp E, Kibaroglu A, et al. Oligoclonal T cell expansions in patients with Behcet's disease[J]. Clin Exp Immunol, 1999, 117(1): 166-170.
  • 9Hwang HY, Bahk YY, Kim TG, et al. Identification of a commonly used CDR3 region of infiltrating T cells expressing Vbeta13 and Vbeta15 derived from psoriasis patients[J]. J Invest Dermatol, 2003, 120(3): 359-364.
  • 10Kalergis AM, Nathenson SG. Altered peptide ligand-mediated TCR antagonism can be modulated by a change in a single amino acid residue within the CDR3 beta of an MHC class I-restricted TCR[J]. J Immunol, 2000, 165(1): 280-285.

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  • 1彭其胜,李月红,朱平.IL-10_(18-57)-PE40高效表达、纯化及细胞活性之研究[J].生物工程学报,2006,22(1):87-93. 被引量:4
  • 2Brioschi A, Zenga F, Zara GP, et al. Solid lipid nanoparticles : could they help to improve the efficacy of pharmacologic treatments for brain tumors? Neurol Res, 2007 , 29 ( 3 ) : 324-330.
  • 3Lu W, Zhang Y, Tan YZ, etal . Cationic albumin - conjugated pegylated nanoparticles as novel drug carrier for brain delivery. J Control Release, 2005 , 107 ( 3 ) :428-498.
  • 4Costantino L, Gandolfi F, Tosi G, et al. Peptide-derivatized biodegradable nanoparticles able to cross the blood-brain barrier. J Control Rel, 2005 , 108 ( 1 ) : 84-96.
  • 5Wohlgemuth M, Machtle W, Mayer C. Improved preparation and physical studies of polybutylcyanoacrylate nanocapscules. J Microencapsul, 2000,17 ( 4 ) : 437 -448.
  • 6Kreuter J, Alyautdin RN, Kharkevich DA, et al. Passage of peptides through the blood-brain barrier with colloidal polymer particles (nanoparticles). Brain Res, 1995, 674 ( 1 ) : 171-174.
  • 7Gao K, Jiang X, Influence of particle size on transport of methotrexate across blood-brain barrier by polysorbate 80-coated polybutylcyanoacrylate-nanoparticles. Int J Phann ,2006, 310(1-2) : 213-219.
  • 8Das D, Lin S. Double-coated poly (butylcynanoacrylate) nanoparticulate delivery systems for brain targeting of dalargin via oral administration. J Pharm Sci, 2005, 94 (6): 1343-1353.
  • 9Wilson CB, The Gliomas. USA : W. B. Saunders company, 1999, 115-123.
  • 10Garcia-Garcia E, Andrieux K, Gil S, et al. Colloidal carriers and blood-brain barrier translocation: a way to deliver drugs to the brain ? Int J Pharm, 2005, 298(2) : 274- 292.

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