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与癌胚抗原(CEA)相关的单克隆抗体定义表位的定位

Mapping of monoclonal antibody-defined epitopes associated with carcinoembryonic antigen, CEA.

作者信息

Price M R, Edwards S, Jacobs E, Pawluczyk I Z, Byers V S, Baldwin R W

出版信息

Cancer Immunol Immunother. 1987;25(1):10-5. doi: 10.1007/BF00199295.

Abstract

Six immunoglobulin G monoclonal antibodies reactive with carcinoembryonic antigen (CEA) were evaluated with respect to parameters implicated in their potential diagnostic application and use as tumor targeting agents for cytotoxic drugs or plant or bacterial toxins. Antibody reactivity with surface antigens of the MKN-45 gastric tumor cell line was demonstrated by flow cytofluorimetry. In a subcellular membrane binding assay, each antibody reacted preferentially with membranes isolated from colorectal tumor tissue in comparison with their reaction with membranes from adjacent, apparently normal colonic mucosa. Three of the antibodies (NCRC-23, C228, and 11.285.14) reacted specifically with CEA with little or no reaction with the cross-reacting antigen, NCA. The remaining three antibodies (C24, C161, and C198) were reactive with both CEA and NCA. Analysis of the epitopes defined by these antibodies was performed by competitive binding inhibition assays evaluating the capacity of unlabeled antibodies to compete with 125I-labeled antibodies in their binding to CEA. In addition, double determinant or 'sandwich' radioimmunoassays were employed to examine the coexpression of epitopes on CEA molecules. These studies permitted an epitope map to be constructed which describes the coincidence, overlapping, or independent expression of both CEA specific epitopes and epitopes shared between CEA and NCA. The map may be employed for the selection of antibodies for diagnostic and therapeutic use.

摘要

对六种与癌胚抗原(CEA)反应的免疫球蛋白G单克隆抗体进行了评估,评估内容涉及与其潜在诊断应用相关的参数,以及用作细胞毒性药物、植物或细菌毒素的肿瘤靶向剂的用途。通过流式细胞荧光术证明了抗体与MKN - 45胃肿瘤细胞系表面抗原的反应性。在亚细胞膜结合试验中,与它们与相邻的、看似正常的结肠黏膜膜的反应相比,每种抗体都优先与从结直肠肿瘤组织中分离的膜发生反应。其中三种抗体(NCRC - 23、C228和11.285.14)与CEA特异性反应,与交叉反应抗原NCA几乎没有或没有反应。其余三种抗体(C24、C161和C198)与CEA和NCA都有反应。通过竞争性结合抑制试验分析这些抗体所定义的表位,该试验评估未标记抗体在与CEA结合时与125I标记抗体竞争的能力。此外,采用双决定簇或“夹心”放射免疫测定法来检测CEA分子上表位的共表达。这些研究使得能够构建一个表位图,该图描述了CEA特异性表位以及CEA和NCA之间共享的表位的重合、重叠或独立表达情况。该图可用于选择用于诊断和治疗的抗体。

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