一种人单克隆抗体,具有中和金黄色葡萄球菌α毒素的能力。

N. Heveker, A. Hansen, K. Hungerer, R. von Baehr, R. Glaser
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引用次数: 3

摘要

利用杂交瘤技术建立了抗葡萄球菌α -毒素的人单克隆抗体CB STL-1。它属于IgG1亚类,具有λ轻链,解离常数为8 × 10(-10) mol/l。在兔红细胞体外溶血试验中,1mg纯化抗体可中和800微克/毫升α毒素的溶血活性。该抗体不与跨越α毒素序列的重叠(7个残基)十肽结合,因此它可能与构象表位结合。抗体识别的抗原表位在寡聚毒素中是不可接近的。抗体与单体毒素的亲水性和两亲性结合,抗体的Fab片段是稳定的,没有明显的活性损失。cbstl -1在小鼠体内对α毒素的i.p.攻击具有保护作用。因此,该抗体是被动免疫治疗的候选抗体。对CB STL-1分泌的抗体可变区进行测序,发现其编码的VH基因片段属于VH1家族,而Vlambda片段很可能属于VlambdaIII亚群。进一步分析了重链的第三互补决定区(CDR3)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A human monoclonal antibody with the capacity to neutralize Staphylococcus aureus alpha-toxin.
A human monoclonal antibody, CB STL-1, against staphylococcal alpha-toxin has been established by hybridoma technology. It is of IgG1 subclass with lambda light chain and possesses a dissociation constant of 8 x 10(-10) mol/l. 1 mg of purified antibody neutralizes the hemolytic activity of 800 micrograms/ml alpha-toxin in an in vitro hemolysis assay using rabbit erythrocytes. The antibody does not bind to overlapping (7 residues) decapeptides spanning the sequence of alpha toxin, thus it might bind to a conformational epitope. The epitope recognized by the antibody is not accessible in oligomeric toxin. The antibody binds both to the hydrophilic and amphipathic forms of the monomeric toxin Fab fragments of the antibody are stable and show no significant loss of activity. CB STL-1 was able to protect mice in vivo from i.p. challenge with alpha toxin. Thus, the antibody is a candidate for passive immunotherapy. The variable regions of the antibody secreted by CB STL-1 were sequenced and found to be encoded by a VH gene segment belonging to the VH1 family, and a Vlambda segment most likely belonging to the VlambdaIII subgroup. Further analysis concerning the third complementarity determining region (CDR3) of the heavy chain is presented.
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