首页> 美国卫生研究院文献>Journal of Virology >Identification of Chimpanzee Fab Fragments by Repertoire Cloning and Production of a Full-Length Humanized Immunoglobulin G1 Antibody That Is Highly Efficient for Neutralization of Dengue Type 4 Virus
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Identification of Chimpanzee Fab Fragments by Repertoire Cloning and Production of a Full-Length Humanized Immunoglobulin G1 Antibody That Is Highly Efficient for Neutralization of Dengue Type 4 Virus

机译:通过库克隆和高效中和登革热4型病毒的全长人源化免疫球蛋白G1抗体的生产来鉴定黑猩猩的Fab片段。

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摘要

A safe and effective dengue vaccine is still not available. Passive immunization with monoclonal antibodies from humans or nonhuman primates represents an attractive alternative for the prevention of dengue virus infection. Fab monoclonal antibodies to dengue type 4 virus (DENV-4) were recovered by repertoire cloning of bone marrow mRNAs from an immune chimpanzee and analyzed for antigen binding specificity, VH and VL sequences, and neutralizing activity against DENV-4 in vitro. Fabs 5A7, 3C1, 3E4, and 7G4 were isolated from a library constructed from a chimpanzee following intrahepatic transfection with infectious DENV-4 RNA. Fabs 5H2 and 5D9, which had nearly identical VH sequences but varied in their VL sequences, were recovered from a library constructed from the same chimpanzee after superinfection with a mixture of DENV-1, DENV-2, and DENV-3. In radioimmunoprecipitation, Fab 5A7 precipitated only DENV-4 prM, and Fabs 3E4, 7G4, 5D9, and 5H2 precipitated DENV-4 E but little or no prM. Fab 3E4 and Fab 7G4 competed with each other for binding to DENV-4 in an enzyme-linked immunosorbent assay, as did Fab 3C1 and Fab 5A7. Fab 5H2 recognized an epitope on DENV-4 that was separate from the epitope(s) recognized by other Fabs. Both Fab 5H2 and Fab 5D9 neutralized DENV-4 efficiently with a titer of 0.24 to 0.58 μg/ml by plaque reduction neutralization test (PRNT), whereas DENV-4-neutralizing activity of other Fabs was low or not detected. Fab 5H2 was converted to full-length immunoglobulin G1 (IgG1) by combining it with human sequences. The humanized chimpanzee antibody IgG1 5H2 produced in CHO cells neutralized DENV-4 strains from different geographical origins at a similar 50% plaque reduction (PRNT50) titer of 0.03 to 0.05 μg/ml. The DENV-4 binding affinities were 0.42 nM for Fab 5H2 and 0.24 nM for full-length IgG1 5H2. Monoclonal antibody IgG1 5H2 may prove valuable for passive immunoprophylaxis against dengue virus in humans.
机译:尚无安全有效的登革热疫苗。用人类或非人类灵长类动物的单克隆抗体进行被动免疫是预防登革热病毒感染的一种有吸引力的选择。通过从免疫黑猩猩中克隆骨髓mRNA的方法,回收了针对登革热4型病毒(DENV-4)的Fab单克隆抗体,并在体外分析了抗原结合特异性,VH和VL序列以及对DENV-4的中和活性。在用感染性DENV-4 RNA进行肝内转染后,从由黑猩猩构建的文库中分离出Fabs 5A7、3C1、3E4和7G4。在用DENV-1,DENV-2和DENV-3混合感染后,从同一只黑猩猩构建的文库中回收了具有几乎相同的VH序列但VL序列不同的Fab 5H2和5D9。在放射免疫沉淀中,Fab 5A7仅沉淀DENV-4 prM,而Fab 3E4、7G4、5D9和5H2沉淀DENV-4 E,但仅沉淀很少或没有prM。 Fab 3E4和Fab 7G4在酶联免疫吸附试验中相互竞争与DENV-4的结合,Fab 3C1和Fab 5A7也是如此。 Fab 5H2识别DENV-4上的一个表位,该表位与其他Fab识别的一个或多个表位分开。通过噬斑减少中和测试(PRNT),Fab 5H2和Fab 5D9均以0.24至0.58μg/ ml的效价有效中和DENV-4,而其他Fab的DENV-4中和活性较低或未检测到。通过将Fab 5H2与人序列结合,将其转化为全长免疫球蛋白G1(IgG1)。在CHO细胞中产生的人源化黑猩猩抗体IgG1 5H2以0.03至0.05μg/ ml的相似的50%噬斑减少(PRNT50)滴度中和了来自不同地理区域的DENV-4菌株。 DENV-4结合亲和力对于Fab 5H2为0.42 nM,对于全长IgG1 5H2为0.24 nM。单克隆抗体IgG1 5H2可能对于被动免疫预防登革热病毒具有重要意义。

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