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一种具有人癌胚抗原特异性表位镜像的单克隆抗独特型抗体。

A monoclonal anti-idiotypic antibody bearing the image of an epitope specific to the human carcinoembryonic antigen.

作者信息

Gaida F J, Fenger U, Wagener C, Neumaier M

机构信息

Dept. of Clinical Chemistry, Universitätskrankenhaus Eppendorf, Hamburg, Germany.

出版信息

Int J Cancer. 1992 May 28;51(3):459-65. doi: 10.1002/ijc.2910510320.

Abstract

One concept for immune therapy of patients bearing carcinomas involves monoclonal anti-idiotypic antibodies (Malds) to trigger the immune system of the host into a response against the tumor cells. Current theory states that so-called internal image Malds bearing epitopes specific to a given tumor-associated antigen would be most suited for that purpose. We report here the generation of syngeneic Malds generated against the murine monoclonal immunoglobulin T84.66 (Ab1), which defines a single epitope on the protein moiety of the carcinoembryonic antigen (CEA). This antigenic determinant is unique to CEA, as it is absent in other members of the CEA gene family that are expressed in a variety of normal human tissues, including granulocytes. The Mald 6G6.C4 (Ab2) exhibits the immunochemical features of an internal image antibody mimicking the epitope recognized by the idiotype T84.66. In enzyme immunoassays the binding of Ab1 to Ab2 is completely inhibited by CEA. In addition, Mald 6G6.C4 only binds to native but not to the denatured or reduced idiotype. Immunization of rabbits with F(ab')2-fragments of 6G6.C4 results in antisera (Ab3) that show specificity to CEA in both binding and inhibition enzyme immunoassays as well as in Western blots. Finally, Ab3 did not detect NCA, a major CEA-related glycoprotein in Western blots, either in a purified form or in a crude tumor extract, indicating a high specificity of the anti-anti-idiotypic response. In summary, these immunochemical data show that the monoclonal anti-idiotype 6G6.C4 can functionally mimic a CEA-specific epitope in rabbits and may do so in humans. Therefore, this antibody may have a clinical potential as a network antigen for active immune therapy in patients suffering from CEA-positive carcinomas.

摘要

一种针对患有癌症的患者的免疫治疗概念涉及使用单克隆抗独特型抗体(Malds)来触发宿主的免疫系统对肿瘤细胞产生反应。当前理论认为,所谓的携带特定肿瘤相关抗原表位的内影像Malds最适合此目的。我们在此报告针对鼠单克隆免疫球蛋白T84.66(Ab1)产生的同基因Malds,该抗体定义了癌胚抗原(CEA)蛋白质部分上的一个单一表位。这种抗原决定簇是CEA所特有的,因为在CEA基因家族的其他成员中不存在,这些成员在包括粒细胞在内的多种正常人体组织中表达。Mald 6G6.C4(Ab2)表现出模拟独特型T84.66识别的表位的内影像抗体的免疫化学特征。在酶免疫测定中,CEA完全抑制Ab1与Ab2的结合。此外,Mald 6G6.C4仅与天然的独特型结合,而不与变性或还原的独特型结合。用6G6.C4的F(ab')2片段免疫兔子产生抗血清(Ab3),该抗血清在结合和抑制酶免疫测定以及蛋白质印迹中均显示出对CEA的特异性。最后,Ab3在蛋白质印迹中未检测到NCA(一种主要的CEA相关糖蛋白),无论是纯化形式还是粗肿瘤提取物中,这表明抗抗独特型反应具有高度特异性。总之,这些免疫化学数据表明,单克隆抗独特型抗体6G6.C4在兔子中可在功能上模拟CEA特异性表位,在人类中可能也是如此。因此,这种抗体作为CEA阳性癌症患者主动免疫治疗的网络抗原可能具有临床潜力。

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