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抗乙型肝炎病毒S抗原全人单克隆抗体的制备和表位探究 被引量:2
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作者 佀传亚 潘少坤 +4 位作者 凌志洋 伊春艳 邓志瑞 谢幼华 孙兵 《中国免疫学杂志》 CAS CSCD 北大核心 2018年第7期1029-1033,共5页
目的:针对乙型肝炎病毒S蛋白,制备全人单克隆抗体,对其亲和力、中和病毒活性及抗体所结合的抗原表位进行研究。所制备的全人抗体可应用于乙肝病毒的暴露后预防,为阻断母婴传播提供治疗手段。方法:通过流式分选和单细胞RT-PCR技术获得单... 目的:针对乙型肝炎病毒S蛋白,制备全人单克隆抗体,对其亲和力、中和病毒活性及抗体所结合的抗原表位进行研究。所制备的全人抗体可应用于乙肝病毒的暴露后预防,为阻断母婴传播提供治疗手段。方法:通过流式分选和单细胞RT-PCR技术获得单克隆抗体;利用间接ELISA法检测抗体结合活性,进行表位分析;Hep G2-NTCP细胞用于病毒感染,KHB乙型肝炎病毒e抗原诊断试剂盒检测细胞上清中HBe Ag的指标。结果:获得三株具有中和活性,可以结合三种乙肝病毒亚型S蛋白的抗体,其中1F2、2A1两株抗体的结合依赖于抗原蛋白的天然构象,2H2抗体的结合依赖于连续的氨基酸序列;1F2、2H2抗体结合的位置位于S蛋白胞外区第一个免疫环状区域。结论:利用单细胞RT-PCR技术成功制备了针对乙肝病毒S蛋白的抗体,其具有中和作用。抗原表位位于S蛋白胞外区的第一个免疫环状区域内。 展开更多
关键词 乙型肝炎 全人单克隆抗体 单细胞RT-PCR 中和活性 抗体表位
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Effects of RRA Treatments on Microstructures and Properties of a New High-strength Aluminum-Lithium Alloy-2A97 被引量:6
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作者 YUAN Zhi-shan LU Zheng +2 位作者 xie you-hua DAI Sheng-long LIU Chang-sheng 《Chinese Journal of Aeronautics》 SCIE EI CAS CSCD 2007年第2期187-192,共6页
A new high strength 2A97 Al-Cu-Li-X alloy was subjected to triple-aging of retrogression and re-aging treatments (RRA). Transmission electron microscopy (TEM), differential scanning calorimetry (DSC), and tensil... A new high strength 2A97 Al-Cu-Li-X alloy was subjected to triple-aging of retrogression and re-aging treatments (RRA). Transmission electron microscopy (TEM), differential scanning calorimetry (DSC), and tensile tests were used to investigate the effects of RRA treatment on the microstructures and properties. DSC test reveals the reversion temperature range of the strengthening δ' (Al3Li) phase. The results show that the microstructure consists of δ' (Al3Li) phase, T1 (Al2CuLi) phase and θ″/θ′(Al2Cu) phase for 2A97 alloy treated by a triple-aging of a retrogression and re-aging treatment in the following order: (1) at 165℃×30 min, (2) at 220 ℃ or 240℃ × 15 min, (3) at 165℃×24 h. The plastic deformation, incorporated into the treatment after secondary high temperature aging, promotes the T1 precipitation during final re-aging. The tensile properties of the alloy treated by the retrogression and re-aging treatment reach the peak level of alloy single-aged at 165℃ in T6 temper. 展开更多
关键词 2A97 Al-Cu-Li-X alloy RRA treatments triple aging microstructure REVERSION
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Immunization with HBsAg-Fc fusion protein induces a predominant production of Thl cytokines and reduces HBsAg level in transgenic mice 被引量:3
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作者 MENG Zhe-feng WANG Hua-jing +5 位作者 YAO Xin WANG Xuan-yi WEN Yu-mei DAI Jian-xin xie you-hua XU Jian-qing 《Chinese Medical Journal》 SCIE CAS CSCD 2012年第18期3266-3272,共7页
Background The Fc receptor associated pathway might improve the immune responses against hepatitis B virus (HBV) as previously described by us. In addition, the Fit3 ligand (FL) has been reported to potentiate ant... Background The Fc receptor associated pathway might improve the immune responses against hepatitis B virus (HBV) as previously described by us. In addition, the Fit3 ligand (FL) has been reported to potentiate antigen presenting cells in vivo and may act as a potential adjuvant to boost antigen-specific immune responses. In this study, the immune efficacies of a set of fusion proteins of HBsAg and Fc and/or FL were evaluated in HBsAg transgenic mice. Methods The fusion proteins composed of HBsAg and the Fc domain of murine IgG1 (HBsAg-Fc) and/or the Fit3 ligand, and yeast-derived recombinant HBsAg were used as immunogen to immunize HBsAg transgenic mice, respectively. Serum and liver HBsAg levels, serum anti-HBsAg and cytokine profile, and the activities of alanine aminotransferase (ALT)/AST were investigated after immunization. Results After six injections, the most pronounced decrease in serum and liver HBsAg levels was observed in the HBsAg-Fc immunized group. In addition, serum Thl cytokines and ALT/AST activities were highest in this group, indicating an effective induction of a favorable cellular immune response. Interestingly, the fusion protein containing HBsAg-Fc and the Fit3 ligand stimulated an alternative Thl-type immune response featured with high level productions of tumor necrosis factor a (TNF-a) and monocyte chemoabstractant protein 1 (MCP-1), causing a more severe cytotoxicity in hepatocytes while showed less effective in reducing serum HBsAg level. Conclusion HBsAg-Fc is effective in eliciting both the humeral and cellular immune responses against HBsAg in HBsAg transgenic mice, which makes it a potential immunogen for the immunotherapy of chronic hepatitis B. 展开更多
关键词 Fc receptor hepatitis B surface antigen transgenic mice hepatitis B virus therapeutic vaccine
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