文章摘要
李慧瑾,孙丽君,孙晶莹,赵向绒,梁导艳,李 元,胡 军.三株交叉反应性的流感病毒HA抗体与H1N1流感病毒的致病机制分析[J].,2019,19(16):3068-3072
三株交叉反应性的流感病毒HA抗体与H1N1流感病毒的致病机制分析
Pathogenic Mechanism of Three Cross Reactive Influenza Virus HA Antibodies and H1N1 Influenza Virus
投稿时间:2019-03-07  修订日期:2019-03-30
DOI:10.13241/j.cnki.pmb.2019.16.012
中文关键词: H1N1流感病毒  血凝素  红细胞  淋巴细胞  血小板
英文关键词: H1N1 influenza virus  Hemagglutinin  Red blood cell(RBC)  Lymphocytes  Platelet(PLT)
基金项目:国家自然科学基金项目(81202373);陕西省教育厅2018年度重点科学研究计划项目(18JS103);西安医学院2017博士启动基金项目(2017DOC02);西安医学院2018 年国家基金培育项目(2018GJFY09);陕西省科技厅一般项目-社会发展(2017SF-270)
作者单位E-mail
李慧瑾 1陕西省缺血性心血管疾病重点实验室西安医学院基础与转化医学研究所 陕西 西安 7100212陕西省人民医院中心实验室 陕西 西安 710062 187085591@qq.com 
孙丽君 陕西省人民医院中心实验室 陕西 西安 710062  
孙晶莹 陕西省人民医院中心实验室 陕西 西安 710062  
赵向绒 陕西省人民医院中心实验室 陕西 西安 710062  
梁导艳 陕西省人民医院中心实验室 陕西 西安 710062  
李 元 陕西省人民医院中心实验室 陕西 西安 710062  
胡 军 陕西省人民医院中心实验室 陕西 西安 710062  
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中文摘要:
      摘要 目的:结合临床甲型流感病例分析流感病毒可能的致病机理。方法:收集87份陕西省2009年甲型H1N1流感重症,危重症及死亡病例的血常规参数,对其淋巴细胞、红细胞和血小板三个指标分析。制备针对甲型H1N1的单克隆抗体,采用抗体亚类鉴定试剂盒分析其抗体轻链和重链的亚型,通过血凝活性实验检测三株抗体的血凝抑制活性,通过ELISA检测三株抗体与人和小鼠的血红蛋白、红细胞、白细胞膜和血小板膜的反应,通过免疫组化分析三株流感病毒抗体与正常小鼠肺组织的结合。结果:流感病毒感染后的死亡病例中淋巴细胞、红细胞和血小板均明显降低。三株抗体与人和小鼠的淋巴细胞、红细胞和血小板均有不同程度的交叉反应;免疫组化结果同时也证实三株HA抗体与小鼠的肺组织有不同的结合力。结论:流感病毒致病的原因可能与流感病毒感染机体后产生的抗体可与血液和组织中的成分结合有关。
英文摘要:
      ABSTRACT Objective: To analyze the possible pathogenesis of influenza virus based on clinical influenza A cases and three mAbs against H1N1-HA. Methods: The binding sites of the two antibodies with HA were analyzed by phage display library. Polypeptide synthesis based on the selected antigenic sites and HA sequence, monoclonal antibodies prepared by immunization mice with two polypeptide, light chain and heavy chain variable region of four antibodies were obtained by means of molecular cloning. Moreover, the binding domain of antibodies and antigen was predicted by computer simulation. Blood routine parameters of 87 severe, critical and fatal cases of influenza A (H1N1) in Shaanxi Province in 2009 were collected and their lymphocyte, erythrocyte and platelet indices were analyzed. Three mAbs against H1N1-HA were prepared by our lab, the subtypes of light and heavy chains of antibodies were analyzed by antibody subclass identification kit. The hemagglutination inhibition of the three antibodies was tested by hemagglutination activity test. The reactions of the three antibodies with human and mouse hemoglobin, erythrocyte, leukocyte and platelet membranes were detected by ELISA. The binding of three influenza virus antibodies to normal mice lung tissue was analyzed by immunohistochemistry. Results: The lymphocytes, red blood cells and platelets in the death cases were significantly decreased inafter influenza virus infection. ELISA results showed that the three antibodies had different cross-reactivity with human and mouse lymphocyte, erythrocyte and platelet. The three antibodies had different cross-reactivity with human and mouse lymphocytes, erythrocytes and platelets. The results of immunohistochemistry also confirmed that the three HA antibodies had different binding capacity with mouse lung tissue. Conclusion: The pathogenesis of influenza virus may be related to the combination of antibodies produced by influenza virus infection with blood and tissue components.
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