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巨球蛋白血症患者中出现单克隆IgA及一种明显的IgG:IgM、IgA和IgG之间个体特异性抗原决定簇的共享

Development of monoclonal IgA and an apparent IgG in a patient with macroglobulinemia: sharing of individually specific antigenic determinants among IgM, IgA, and IgG.

作者信息

Fair D S, Schaffer S, Krueger R G

出版信息

J Immunol. 1976 Sep;117(3):944-9.

PMID:60453
Abstract

Patient CM, who initially was diagnosed as having macroglobulinemia (IgM, kappa) was subsequently found to develop a monoclonal IgA(kappa) protein. Rabbit antisera directed against the patient's IgAm and IgM were rendered specific for individual antigenic (ind) determinants. The anti-IgAm and IgM ind sera reacted with both 131I labeled monoclonal proteins in a double antibody radioimmunoassay (RIA). In addition, both monoclonal immunoglobulins inhibited the reaction between labeled immunoglobulin and both ind antisera, and statistical analysis of the data suggested that the shared ind determinants were identical. The IgG fraction of patient CM's serum also contained a component which competed with both monoclonal IgA (CM) and IgM (CM) in the RIA specific for ind determinants. Analysis of serum samples taken over a 2-year period revealed that, in addition to IgM, both the IgA and IgG components possessing the shared ind determinant(s) were present in low concentrations in the earliest sample, although not detected by conventional techniques. The monoclonal IgA and the IgG component were found to increase in concentration over this time interval with a concomitant decrease in IgM. The regulation of immunoglobulin expression with respect to the proposed models of gene organization in antibody-producing cells was discussed.

摘要

患者CM最初被诊断为患有巨球蛋白血症(IgM,κ型),随后发现其产生了一种单克隆IgA(κ型)蛋白。针对患者IgAm和IgM的兔抗血清对单个抗原决定簇具有特异性。在双抗体放射免疫分析(RIA)中,抗IgAm和IgM的单个决定簇血清与两种131I标记的单克隆蛋白都发生反应。此外,两种单克隆免疫球蛋白均抑制标记免疫球蛋白与两种单个决定簇抗血清之间的反应,数据的统计分析表明,共享的单个决定簇是相同的。患者CM血清的IgG组分还包含一种在针对单个决定簇的RIA中与单克隆IgA(CM)和IgM(CM)都发生竞争的成分。对两年期间采集的血清样本进行分析发现,除了IgM之外,具有共享单个决定簇的IgA和IgG成分在最早的样本中浓度都很低,尽管用传统技术未检测到。发现单克隆IgA和IgG成分在这个时间间隔内浓度增加,同时IgM减少。讨论了关于抗体产生细胞中基因组织的拟议模型中免疫球蛋白表达的调控。

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