Liang X H, Jiang H H, Levine B
Department of Medicine, Columbia University College of Physicians & Surgeons, New York, NY 10032, USA.
Mol Immunol. 1997 Aug-Sep;34(12-13):907-17. doi: 10.1016/s0161-5890(97)00098-9.
Monoclonal antibodies to the Sindbis virus E2 envelope glycoprotein protect mice against lethal encephalitis and mediate viral clearance from neurons. To facilitate structure-function analyses of anti-E2 mAbs, we developed an expression system that can be used for the construction of genetically engineered anti-E2 mAbs. We constructed recombinant Sindbis/immunoglobulin gene chimeric viruses that express heavy and light chains of an anti-E2 monoclonal antibody, R6. We used a PCR-based strategy to clone the entire rearranged heavy and light chain genes from R6 hybridoma cell cDNA into a double subgenomic Sindbis virus vector. The recombinant viruses, SIN/R6L and SIN/R6H, were generated by transfecting BHK-21 cells with in vitro transcribed RNA from Sindbis virus/R6 light chain and Sindbis virus/R6 heavy chain cDNA clones, respectively. Twelve hours after co-infection of BHK cells with SIN/R6L and SIN/R6H, the tissue culture supernatant contained up to 1.4 mg/ml of recombinant R6 IgG. The heavy and light chains of recombinant R6 were associated as judged by co-purification on protein A/G sepharose and co-electrophoresis of non-reduced proteins. The ELISA reactivity to Sindbis virus antigen was similar for recombinant R6 and R6 purified from ascites fluid. Furthermore, the in vivo biologic activity of recombinant R6 was similar to that of R6 purified from ascites; recombinant R6 treatment completely protected Balb/cJ mice from paralysis and death due to infection with neuroadapted Sindbis virus and also resulted in the clearance of infectious virus from the brains of immunodeficient scid mice persistently infected with wild-type Sindbis virus. Thus, the co-infection of BHK cells with SIN/R6L and SIN/R6H leads to the expression, assembly, and secretion of a biologically active recombinant antiviral antibody. Our results suggest that the Sindbis virus vector system is a simple and powerful tool for the production of functional, genetically engineered antibodies.
针对辛德毕斯病毒E2包膜糖蛋白的单克隆抗体可保护小鼠免受致命性脑炎侵害,并介导病毒从神经元中清除。为便于对抗E2单克隆抗体进行结构-功能分析,我们开发了一种可用于构建基因工程抗E2单克隆抗体的表达系统。我们构建了表达抗E2单克隆抗体R6重链和轻链的重组辛德毕斯/免疫球蛋白基因嵌合病毒。我们采用基于聚合酶链反应(PCR)的策略,将R6杂交瘤细胞cDNA中完整重排的重链和轻链基因克隆到双亚基因组辛德毕斯病毒载体中。重组病毒SIN/R6L和SIN/R6H分别通过用体外转录的来自辛德毕斯病毒/R6轻链和辛德毕斯病毒/R6重链cDNA克隆的RNA转染BHK-21细胞而产生。用SIN/R6L和SIN/R6H共同感染BHK细胞12小时后,组织培养上清液中重组R6 IgG含量高达1.4 mg/ml。通过蛋白A/G琼脂糖凝胶共纯化和非还原蛋白的共电泳判断,重组R6的重链和轻链相互关联。重组R6与从腹水液中纯化的R6对辛德毕斯病毒抗原的酶联免疫吸附测定(ELISA)反应性相似。此外,重组R6的体内生物学活性与从腹水液中纯化的R6相似;重组R6治疗可完全保护Balb/cJ小鼠免受神经适应性辛德毕斯病毒感染所致的麻痹和死亡,还可使持续感染野生型辛德毕斯病毒的免疫缺陷scid小鼠脑中的感染性病毒清除。因此,用SIN/R6L和SIN/R6H共同感染BHK细胞可导致具有生物活性的重组抗病毒抗体的表达、组装和分泌。我们的结果表明,辛德毕斯病毒载体系统是生产功能性基因工程抗体的简单而强大的工具。