Suppr超能文献

针对病理性抗Pr2冷凝集素的抗独特型抗体。

Anti-idiotypic antibodies specific for a pathologic anti-Pr2 cold agglutinin.

作者信息

Jefferies L C, Stevenson F K, Goldman J, Bennett I M, Spitalnik S L, Silberstein L E

机构信息

Department of Pathology, Hospital of the University of Pennsylvania, Philadelphia.

出版信息

Transfusion. 1990 Jul-Aug;30(6):495-502. doi: 10.1046/j.1537-2995.1990.30690333478.x.

Abstract

The heterogeneity of human red cell (RBC) autoantibodies may be assessed by using anti-idiotypic antibodies. In this study, mouse monoclonal anti-idiotypic antibodies were produced against a pathologic RBC autoantibody with anti-Pr2 specificity. Epstein-Barr virus-transformed B-cell clones were established from a patient who had splenic lymphoma and associated immune hemolysis due to an anti-Pr2 cold autoantibody. Two of the eight clones producing this autoantibody were used to immunize mice for the establishment of hybridomas, and four monoclonal anti-idiotypic antibodies were isolated (2 IgG1 kappa and 2 IgM kappa). By the use of these anti-idiotypic antibodies, strong crossreactivity was seen on enzyme-linked immunosorbent assay with other anti-Pr2-producing clones from the same patient, but no cross-reactivity was seen with RBC autoantibodies from other individuals having anti-Pr or different specificities. Each of the anti-idiotypic antibodies inhibited hemagglutination (HA) by the patient's anti-Pr2 but failed to inhibit HA by antisera of a different RBC specificity. Cross-competition experiments indicated that all of the anti-idiotypic antibodies may recognize the same or a closely related idiotope on the anti-Pr2 autoantibody. These studies suggested that the four anti-idiotypic antibodies are directed against the same (or closely related) idiotypic determinant(s), unique to this patient's anti-Pr2 and located at or near the antigen-binding site. These anti-idiotypic antibodies may be useful tools for the study of this autoimmune response or for the development of immune therapeutic agents.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

人类红细胞(RBC)自身抗体的异质性可通过使用抗独特型抗体来评估。在本研究中,针对具有抗Pr2特异性的病理性RBC自身抗体产生了小鼠单克隆抗独特型抗体。从一名患有脾淋巴瘤并因抗Pr2冷自身抗体导致相关免疫性溶血的患者中建立了爱泼斯坦 - 巴尔病毒转化的B细胞克隆。产生这种自身抗体的八个克隆中的两个被用于免疫小鼠以建立杂交瘤,并分离出四种单克隆抗独特型抗体(2种IgG1 κ和2种IgM κ)。通过使用这些抗独特型抗体,在酶联免疫吸附测定中观察到与来自同一患者的其他产生抗Pr2的克隆有强烈的交叉反应,但与来自具有抗Pr或不同特异性的其他个体的RBC自身抗体没有交叉反应。每种抗独特型抗体均抑制患者抗Pr2的血凝反应(HA),但未能抑制具有不同RBC特异性的抗血清的HA。交叉竞争实验表明,所有抗独特型抗体可能识别抗Pr2自身抗体上相同或密切相关的独特型表位。这些研究表明,这四种抗独特型抗体针对的是同一(或密切相关)独特型决定簇,该决定簇是该患者抗Pr2所特有的,位于抗原结合位点或其附近。这些抗独特型抗体可能是研究这种自身免疫反应或开发免疫治疗剂的有用工具。(摘要截短至250字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验