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紫外线减活日本血吸虫尾蚴疫苗免疫小鼠肺部iNOS的表达及其与免疫保护关系的研究

STUDIES ON THE RELATIONSHIP BETWEEN iNOS EXPRESSION IN THE LUNGSOF MICE VACCINATED WITH ULTRAVIOLET ATTENUATED SCHSITOSOMA JAPONICUM CERCARIAE AND ITS PROTECTIVE MECHANISM
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摘要 目的 研究紫外线照射减活日本血吸虫尾蚴疫苗免疫小鼠后肺部诱导型一氧化氮合酶(iNOS)的动态表达及其与保护性免疫的关系。 方法 用紫外线照射减活尾蚴疫苗免疫小鼠,30 d后用尾蚴攻击感染。于感染后第4 d、9 d取免疫小鼠和未免疫小鼠肺脏,用RT-PCR半定量的方法检测各组小鼠肺部iNOS的转录水平;用免疫组化方法确定iNOS在肺部的蛋白表达定位。 结果 正常小鼠肺部无iNOS转录和蛋白表达。免疫小鼠和未免疫小鼠感染血吸虫尾蚴后第4 d肺部iNOS有较高水平的转录表达。感染后第9 d,免疫组小鼠iNOS的表达较第4 d下降,而未免疫组小鼠肺部iNOS的表达消失。免疫组化结果表明,免疫组小鼠肺部炎症病灶细胞中存在iNOS的表达。 结论 移行到肺部的血吸虫童虫能诱导肺部表达iNOS,紫外线减活尾蚴疫苗能促使小鼠肺组织较长时间表达iNOS,iNOS在肺部的持续表达可能与该疫苗使宿主产生的免疫保护力有关。 Objective To study the levels of iNOS expression in lungs of unvaccinated mice and mice vaccinated with ultraviolet attenuated Schisto-soma japonicum cercariae and the relationship between iNOS expression and its protective mechanism in mice. Methods Mice were immunized with ultraviolet attenuated cercariae, 30 days post immunization, total RNA was extracted from the lungs of mice after a challenging infection and iNOS mRNA levels between vaccinated and unvaccinated groups at day 0, day 4, day 9 post infection were compared; Immunohistochemical test was performed to detect the distribution of iNOS in lungs. Results For both vaccinated and unvaccinated mice, there was no expression of iNOS in the lungs before challenging infection, iNOS expression increased significantly at day 4 p. t; At day 9, the expression of iNOS decreased for vaccinated mice, while there was no expression for unvaccinated mice. Result of immunohistochemical test showed that iNOS was mainly located in the inflammatory foci in the lung. Conclusion Schistosomula migrated to the lungs can induce iNOS expression in the organ, ultraviolet attenuated cercariae can prolong iNOS expression in lungs after challenging infection, it is possible that longer expression of iNOS is involved in the protective immunity induced by ultraviolet attenuated cercariae.
出处 《中国寄生虫病防治杂志》 CSCD 2004年第4期226-228,共3页 Chinese Journal of Parasitic Disease Control
关键词 血吸虫 日本 紫外线照射减活尾蚴疫苗 小鼠 INOS Schistosoma japonicum ultraviolet attenuated cercariae mouse iNOS
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参考文献10

  • 1龙小纯,李雍龙,方正明.一氧化氮对日本血吸虫童虫细胞毒作用的研究[J].中国寄生虫学与寄生虫病杂志,2002,20(6):342-344. 被引量:13
  • 2Wynn T, Jankovic D, Hieny S,et al. IL-12 enhances vaccine-induced immunity to Schistosoma mansoni in mice and decreases T helper 2 cytokine expression, IgE production, and tissue eosinophilia[J]. J Immunol,1995,154:4701-4709.
  • 3Wynn T, Oswald IP, Eltoum IA, et al. Elevated expression of Th1 Cytokines and nitric oxide synthase in the lungs of vaccinated mice after challenge infection with Schistosoma mansoni[J]. J Immunol,1994,153:5200-5209.
  • 4Abdallahi OM, Bensalem H, Augier R, et al. Arginase expression in peritoneal macrophages and increase in circulating polyamine levels in mice infected with Schistosoma mansoni[J]. Cell Mol Life Sci,2001,58:1350-1357.
  • 5Kassim OO, Dean DA, Mangold BL, et al. Combined microautographic and histopathologic analysis of the fate of challenge Schistosoma mansoni schistosomula in mice immunized with irradiated cercariae[J]. Am J Trop Med Hyg,1992,47:231-237.
  • 6Ahmed SF, Oswald IP, Caspar P, et al. Development differences determine larval susceptibility to nitric oxide mediated killing in a murine model in a vaccination against Schistosoma mansoni[J]. Infection and Immunity,1997,65: 219-226.
  • 7Oswald IP, Eltoum I, Wynn TA, et al. Endothelial cells are activated by cytokine treatment to kill an intravascular parasite, Schistosoma mansoni, through the production of nitric oxide[J]. Proc Natl Acad USA,1994, 91:999-1003.
  • 8Abdallahi OM, Bensalem H, Dereggi MD,et al. Inhibition of nitric oxide synthase activity reduces liver injury in murine schistosomiasis[J]. Parasitology,2001,122:309-315.
  • 9Piedrafita D, Spithill T, Dalton J, et al. Juvenile fasciola hepatica are resistant to killing in vitro by free radicals compared with larvae of Schistosoma mansoni[J] . Parasite Immunology,2000,22:287-295.
  • 10毛守白.血吸虫生物学与血吸虫病的防治[M](第1版)[M].北京:人民卫生出版社,1991.158,396.

二级参考文献10

  • 1孙卫民 王惠琴.细胞因子研究方法学[M].北京:人民卫生出版社,1998.540-581.
  • 2Cristian B. Nitric oxide and the immune response [J]. Nat Immunol, 2001,2:907 - 914.
  • 3Adams LB, Hibbs JB, Taintor RR, et al. Microbiostatic effect of murine activated macrophages for Toxoplasma gonddi: Role for synthesis of inorganic nitrogen oxides from L-arginine[J]. J Immunol, 1990, 144:2725.
  • 4Oswald IP, Eltoum I, Wynn TA , et al. Endothelial cells are activatecl by cytokine treatment to kill an intracellular parasite, Schistosoma mansoni, through the production of nitric oxide [J]. Proc Natl Acad Sci USA, 1994,91:999 - 1003.
  • 5Olieiva DM, Sila-Teixeira DN, Carmo SA, et al. Role of nitric oxide on human schistosomiasis mansoni: upregulation of in vitro granuloma formation by Nw-nitro-L-arginine methyl ester [J]. Nitric Oxide: Biol Chem, 1998,2:57- 65.
  • 6Oswald IP, Gazzinelli RT, Sher A, et al. IL-10 synergizes with IL-4 and transforming growth factor-β to inhibit macrophage cytotoxic activity[J]. J Immunol, 1992,49:3578-3582.
  • 7Piedrafita D, Spithill TW, Dalton JP, et al. Juvenile Fasciola hepatica are resistant to killing in vitro by free radicals compared with larvae of Schistosoma mansoni [J]. Parasite Immunol, 2000,22:287 - 295.
  • 8Brown GC. Nitric oxide inhibition of eytochrome oxidase and mitochondrial respiration: implication for inflammatory neuroclegenerative and ischaemic pathologies[J]. Mol Cell Biochem, 1997,174:189- 192.
  • 9Gotoh T, Oyadomari S, Mori K, et al. Nitric oxide induced apoptosis in RAW264.7 macrophages by endoplasmic reticulum stress pathway involving ATF6 and CHOP[J]. J Biol Chem, 2002,277:12343 - 12350.
  • 10牛宇欣,李慧珠,张海燕,王凤芸.IFN-γ激活巨噬细胞产生一氧化氮杀伤疟原虫的作用[J].中国寄生虫学与寄生虫病杂志,1997,15(6):335-339. 被引量:20

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