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抗人巨细胞病毒中和性人源基因工程抗体的研究
引用本文:段涛,梁米芳,谷淑燕. 抗人巨细胞病毒中和性人源基因工程抗体的研究[J]. 中华实验和临床病毒学杂志, 2003, 17(3): 247-250
作者姓名:段涛  梁米芳  谷淑燕
作者单位:100052,北京,中国疾病预防控制中心病毒病预防控制所病毒应急技术中心
摘    要:目的 研究抗人巨细胞病毒(HCMV)人源基因工程抗体。方法 采用噬菌体表面展示技术。首先从HCMV感染者外周血中分离淋巴细胞,提取RNA,逆转录后用特异性引物扩增轻、重链基因。然后插入噬菌体载体pComb3,构建噬菌体抗体库。使用纯化的HCMV病毒裂解物对噬菌体抗体库进行4轮富集,然后通过ELISA筛选阳性克隆,并对获得的克隆进行功能鉴定。结果 克隆和表达了3株抗HCMV人源Fab抗体,经ELISA证明均具有抗原结合活性,间接免疫荧光试验证明具有较高的特异性,最后通过病毒中和试验证明其中2株具有中和活性。结论 获得2株抗HCMV人源Fab抗体,具有一定的中和活性,为下一步研究抗HCMV人源全抗体奠定了基础。

关 键 词:巨细胞病毒 基因工程 抗体 中和活性 噬菌体表面展示技术 外周血
修稿时间:2002-09-17

Human anti-HCMV neutralizing Fab antibody generated by phage display library
DUAN Tao,LIANG Mi fang,GU Shu yan. Virus Emergency Biotech Center,Institute for Viral Disease Control and Prevention,Chinese Center for Disease Control and Prevention,Beijing ,China Corresponding anthor:GU Shu yan,E mail: shuyan_gu@sina.com. Human anti-HCMV neutralizing Fab antibody generated by phage display library[J]. Chinese journal of experimental and clinical virology, 2003, 17(3): 247-250
Authors:DUAN Tao  LIANG Mi fang  GU Shu yan. Virus Emergency Biotech Center  Institute for Viral Disease Control  Prevention  Chinese Center for Disease Control  Prevention  Beijing   China Corresponding anthor:GU Shu yan  E mail: shuyan_gu@sina.com
Affiliation:Virus Emergency Biotech Center, Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 100052, China.
Abstract:BACKGROUND: Cloning recombinant human Fab fragment against HCMV for the purpose of prophylaxis and control of HCMV infection. METHODS: The authors constructed a HCMV phage display library with 2 x 10(6) clones, then used purified HCMV viral lysates to pan the library, then screened by ELISA. RESULTS: Three clones showed positive responses in ELISA, they also showed high specificity in IFA, two of them could neutralize HCMV in neutralizing assays. CONCLUSION: The specific binding of Fab antibodies to HCMV was demonstrated by ELISA, IFA and neutralizing activities. These results provide us the basis for further research of neutralizing recombinant human whole IgG molecule.
Keywords:Cytomegalovirus  Bacteriophage M13  Immunoglobulins  Antibodies   monoclonal
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