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RAPID ASSAY OF PHAGE-DERIVED RECOMBINANT HUMAN FABS AS BISPECIFIC ANTIBODIES

机译:快速鉴定噬菌体重组人双歧杆菌抗体。

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摘要

Specific anti-tumor and anti-viral activities can be conferred on lymphocytic and myeloid effector cells by retargeting them with bispecific antibodies. These are antibodies which possess an anti-target binding region and a region capable of binding specific effector cell surface markers, For the rapid evaluation of recombinant human Fabs as bispecific antibodies, we have constructed a vector that allows for the conversion of Fabs into protein A fusion proteins, These can be used to generate bispecific antibodies when complexed to appropriate anti-effector cell immunoglobulins. As a model system, a protein A fusion derivative of a human recombinant anti-herpes simplex virus (HSV) Fab was constructed and complexed to OKT3, a T cell-activating antibody specific for CD3. This complex reduced HSV-2 yields in infected cells by about three logs relative to controls,when incubated on HSV-2-infected cell monolayers in the presence of IL-2-activated lymphocytes. The system described allows for the rapid evaluation of recombinant human Fabs as bispecific antibodies for therapeutic applications. In addition, Fab-protein A fusion proteins can be used in ELISA and other immune-assays with increased sensitivity.
机译:通过用双特异性抗体重新靶向淋巴细胞和髓样效应细胞,可以赋予它们特定的抗肿瘤和抗病毒活性。这些是具有抗靶标结合区和能够结合特异性效应细胞表面标志物的区域的抗体。为了快速评估重组人Fabs作为双特异性抗体,我们构建了一种载体,可将Fabs转化为蛋白A融合蛋白,当与适当的抗效应细胞免疫球蛋白复合时,可用于产生双特异性抗体。作为模型系统,构建了人类重组抗单纯疱疹病毒(HSV)Fab的蛋白A融合衍生物并将其与OKT3(一种对CD3特异的T细胞活化抗体)复合。当在IL-2活化的淋巴细胞存在下,在感染了HSV-2的细胞单层上孵育时,这种复合物相对于对照,可使感染细胞中的HSV-2产量降低约3个对数。所描述的系统允许快速评估重组人Fabs作为用于治疗应用的双特异性抗体。另外,Fab-蛋白A融合蛋白可以提高灵敏度用于ELISA和其他免疫测定。

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