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向莹, 陈 松, 李俊华, 钟 山, 王婉瑜, 熊郁良, 陈 实. 2008: 云南孟加拉种眼镜蛇蛇毒因子在灵长类动物内应用的免疫原性研究. 动物学研究, 29(5): 511-517. DOI: 10.3724/SP.J.1141.200805511
引用本文: 向莹, 陈 松, 李俊华, 钟 山, 王婉瑜, 熊郁良, 陈 实. 2008: 云南孟加拉种眼镜蛇蛇毒因子在灵长类动物内应用的免疫原性研究. 动物学研究, 29(5): 511-517. DOI: 10.3724/SP.J.1141.200805511
XIANG Ying, CHEN Song, LI Jun-hua, ZHONG Shan, WANG Wan-yu, XIONG Yu-lang, Chen. 2008. Immunogenicity of Yunnan-cobra Venom Factor in Non-human Primates. Zoological Research, 29(5): 511-517. DOI: 10.3724/SP.J.1141.200805511
Citation: XIANG Ying, CHEN Song, LI Jun-hua, ZHONG Shan, WANG Wan-yu, XIONG Yu-lang, Chen. 2008. Immunogenicity of Yunnan-cobra Venom Factor in Non-human Primates. Zoological Research, 29(5): 511-517. DOI: 10.3724/SP.J.1141.200805511

云南孟加拉种眼镜蛇蛇毒因子在灵长类动物内应用的免疫原性研究

Immunogenicity of Yunnan-cobra Venom Factor in Non-human Primates

  • 摘要: 眼镜蛇蛇毒因子(CVF)能特异性清除机体循环中的补体C3,从而可能在防治补体介导的损伤或疾病中发挥重要的治疗作用。云南孟加拉种眼镜蛇蛇毒因子(Y-CVF)较文献报道的其他各种CVF具有更高的活性和较少的用药量。为探讨Y-CVF静脉使用是否诱导灵长类动物体内产生特异性中和抗体和异种天然抗体,给2只正常食蟹猴每两周静脉注射一次治疗剂量(0.05 mg/kg)的Y-CVF,共4次,检测注射前后不同时间点血清内补体C3水平、总补体活性(CH50)、抗Y-CVF抗体和抗猪内皮细胞异种抗体的变化。结果显示,前2次注射Y-CVF后均有良好的清除补体效果,第 

    Abstract: Cobra venom factor (CVF) depletes complement C3 and may therefore be important in preventing the complement-mediated damage and disease. In comparison with various CVF reported previously, Yunnan-cobra venom factor (Y-CVF) has higher anticomplement activity. The goal for this research is to investigate whether Y-CVF could induce the specific neutralized anti-Y-CVF antibody and xenoantibodies in non-human primates. Thus two cynomolgus monkeys were intravenously injected with Y-CVF (0.05 mg/kg) every two weeks for totally four times. The serum C3, CH50, anti-Y-CVF antibody and xenoantibody levels were measured at different time points before and after Y-CVF injection. The results revealed that, complement C3 was effectively depleted during the first two injections, and incompletely depleted during the third injection, but almost not depleted during the last injection. The results of Western blot and ELISA confirmed the production of anti-Y-CVF antibody, and its titer increased with the injection. Additionally no significant changes of anti-porcine endothelia cell xenoantibodies were found measured by flow cytometry. We concluded that multiple injection of Y-CVF stimulated anti-Y-CVF antibody production in monkeys, which resulted in the invalid of Y-CVF. The induction of anti-alpha -Gal xenoantibody by Y-CVF in primates was not observed.

     

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