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特异性IgG抗体在同源与异种疟原虫再感染中的作用研究 被引量:1

The effect of specific IgG antibody in re-infected with homologous or heterogenic Plasmodium
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摘要 目的探讨特异性IgG抗体在同源和异种疟原虫再感染过程中的作用。方法DBA/2小鼠经腹腔感染致死型约氏疟原虫(Py17XL)60d后,采用等量Py17XL、Py17XNL、Pynigeriensis或PbANKA分别再次攻击,计数红细胞感染率;采用ELISA方法动态检测脾细胞培养上清中IFN-γ及其血清中特异性IgG抗体水平的变化。结果Py17XNL和Pynigeriensis再感染小鼠出现一过性低水平的原虫血症;再感染后第4d脾细胞培养上清中IFN-γ水平与正常小鼠相比无显著性差异(P>0.05),而血清中特异性IgG抗体水平明显升高(P<0.01),小鼠全部存活。相比,PbANKA再感染小鼠出现高水平的原虫血症,与其初次感染水平相近,再感染后第4d脾细胞培养上清中IFN-γ水平出现明显升高(P<0.01),而血清中特异性的IgG抗体水平却无明显变化,与正常小鼠水平接近,小鼠全部死亡。结论特异性IgG抗体可在宿主抗同源疟原虫再感染中发挥着重要作用,而对异种疟原虫再感染无保护性。 To investigate the effect of specific IgG antibody in re infected with homologous or heterogenic Plasmodium. DBA/2 mice were infected by intraperitoneal injection with 1 × 10^6virulent Py17XL parasitized erythroeytes. After 60 days, mice were subsequently re-infected with Pyl7XL, Py17XNL, Py nigeriensis or PbANKA, and then the ratio of infected RBC was counted; The levels of splenoeyte IFN-γ and serous IgG were dynamically detected by ELISA. It was found that DBA/2 mice from re-infected with Pyl7XNL or Py nigeriensis showed low levels and transient parasitemia, the level of IFN-γ in spleen cell supernatants didn't increased significantly on day 4 pi compared with control group (P〉0.05) ; however, the level of specific IgG in serum obviously elevated (P〈0.01), and all mice survived. In contrast, DBA/2 mice from re-infected with PbANKA showed the high level of parasitemia and the same as that of primary infection; the level of IFN-γin spleen cell supernatants significantly increased on day 4 pi compared with control group (P〈0.01) ; however, the level of specific IgG in serum didn't obviously elevated (P〈0.01), and all mice died. These results indicate that as a main effeetor, specific IgG play a key role against re-infected with homologous Plasmodium, but haven't protection against re-infected with heterogenic Plasmodium.,
出处 《中国人兽共患病学报》 CAS CSCD 北大核心 2009年第4期358-360,共3页 Chinese Journal of Zoonoses
关键词 特异性IGG 啮齿类疟原虫 再感染 specific IgG rodent Plasmodium re-infection
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