Gilliland L K, Clark M R, Waldmann H
Department of Pathology, University of Cambridge, United Kingdom.
Proc Natl Acad Sci U S A. 1988 Oct;85(20):7719-23. doi: 10.1073/pnas.85.20.7719.
Previous studies have demonstrated that bispecific hybrid antibodies produced by cell-cell fusion or chemically conjugated heteroaggregates can direct cytotoxic T lymphocytes to kill target cells for which they have no intrinsic specificity, a phenomenon we call effector cell retargeting (ECR). These studies used bispecific reagents with one specificity directed to CD3 or Ti on the effector cell and the other directed to a target cell antigen. To avoid the need to create different hybrid hybridomas for each target antigen we have developed a universal means to elicit ECR through the use of an antiglobulin step. We have constructed a bispecific hybrid antibody with dual specificity for CD3 and a rat immunoglobulin light chain allotype. This bispecific antibody could mediate ECR to a range of target cells, each coated with distinct surface-binding rat monoclonal antibodies. A particular advantage of targeting to surface-bound monoclonal antibodies is that all other available effector systems may also attack the same antibody-coated target cell.
先前的研究表明,通过细胞-细胞融合或化学偶联异聚体产生的双特异性杂交抗体可引导细胞毒性T淋巴细胞杀死它们本身并无内在特异性的靶细胞,我们将这一现象称为效应细胞重定向(ECR)。这些研究使用的双特异性试剂,一种特异性针对效应细胞上的CD3或Ti,另一种针对靶细胞抗原。为避免针对每种靶抗原都要制备不同的杂交杂交瘤,我们开发了一种通用方法,通过抗球蛋白步骤引发ECR。我们构建了一种对CD3和大鼠免疫球蛋白轻链同种异型具有双重特异性的双特异性杂交抗体。这种双特异性抗体可介导对一系列靶细胞的ECR,每个靶细胞都包被有不同的表面结合大鼠单克隆抗体。靶向表面结合单克隆抗体的一个特别优势是,所有其他可用的效应系统也可能攻击同一个抗体包被的靶细胞。