乙型脑炎病毒特异性单克隆抗体的制备和鉴定。

S H Ma, Y L Lin, Y Y Huang, C I Liu, S S Chen, H Y Chiang, L K Chen
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引用次数: 0

摘要

用免疫小鼠脾细胞与NS-1骨髓瘤细胞融合制备了特异性抗乙型脑炎病毒(JEV)的单克隆抗体(MoAbs)。中山- nih (Na)和台湾3株乙脑病毒,即1965年从患者脑分离到的TL,从Cx分离到的NT109 (JE7)。三带喙蚊(tritaeniorhynchus, 1985)和NT109的空斑纯化克隆RP9用于免疫。使用jev感染的细胞裂解液,通过免疫沉淀和western blotting检测moAbs的特异性。用重组乙脑病毒蛋白作为抗原,用同样的方法对它们进行了证实。Na免疫产生4个抗e、3个抗ns1和3个抗ns3 moab。用台湾乙脑地方毒株免疫小鼠获得17个抗e、3个抗ns1和3个抗ns3特异性单克隆抗体。共获得21个抗e、6个抗ns1和6个抗ns3单克隆抗体。这些moab的同型也被确定和描述。有趣的是,大多数针对RP9产生的moab是IgG1同型的。结果表明,共制备了33种针对乙脑病毒的moab抗体,并对其中部分抗乙脑病毒moab抗体进行了鉴定。这些moab抗体为研究乙脑病毒,特别是台湾本地株的抗原性提供了有力的工具。
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Generation and characterization of Japanese encephalitis virus specific monoclonal antibodies.

Monoclonal antibodies (MoAbs) specifically against Japanese encephalitis virus (JEV) were generated by fusion of immunized mouse spleen cells with NS-1 myeloma cells. Nakayama-NIH (Na) and three Taiwan local strains of JEV, i.e., TL isolated from a patient's brain in 1965, NT109 (JE7) isolated from Cx. tritaeniorhynchus in 1985, and RP9, a plaque purified clone of NT109, were used in the immunization. The specificities of moAbs were determined by immunoprecipitation and western blotting, using JEV-infected cell lysates. They were confirmed by the same methods using recombinant JEV proteins as antigens. From Na immunization, 4 anti-E, 3 anti-NS1 and 3 anti-NS3 moAbs were generated. Seventeen anti-E, three anti-NS1 and three anti-NS3 specific moAbs were generated from mice immunized with Taiwan local JEV strains. Overall 21 anti-E, 6 anti-NS1, and 6 anti-NS3 moAbs were produced and characterized. The isotypes of these moAbs were also determined and described. Interestingly, a majority of the moAbs generated for RP9 were IgG1 isotype. In conclusion, 33 moAbs specific to JEV were generated and characterized, and some of these anti-JEV moAbs were made against Taiwan local isolates. These moAbs provide a powerful tool to study JEV, especially the antigenic properties of Taiwan's local strains.

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Studies on the serological cross-reaction between dengue and Japanese encephalitis. Evaluation of CLO test and polymerase chain reaction for biopsy-dependent diagnosis of Helicobacter pylori infection. Purification and characterization of a 94 KD high molecular weight allergen from house dust mite, Dermatophagoides pteronyssinus. Population cell differentiation of Serratia marcescens on agar surface and in broth culture. [Detection of neutralizing antibodies to Japanese encephalitis virus by enzyme-linked immunosorbent assay (ELISA)].
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