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多发性骨髓瘤和意义未明的单克隆丙种球蛋白病患者血清中副蛋白的常见靶点。

A frequent target of paraproteins in the sera of patients with multiple myeloma and MGUS.

作者信息

Preuss Klaus-Dieter, Pfreundschuh Michael, Ahlgrimm Manfred, Fadle Natalie, Regitz Evi, Murawski Niels, Grass Sandra

机构信息

José-Carreras-Center for Immuno- and Gene Therapy, Department of Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany.

出版信息

Int J Cancer. 2009 Aug 1;125(3):656-61. doi: 10.1002/ijc.24427.

Abstract

Antigenic targets of monoclonal gammopathy of undetermined significance (MGUS) and multiple myeloma (MM) paraproteins might play a role in the pathogenesis of these neoplasms. We screened a human fetal brain-derived macroarray with the IgA or IgG containing sera of 192 consecutive MGUS and MM patients. Twenty-nine of 192 (15.1%) paraproteins reacted with paratarg-7, a protein of unknown function which is expressed in all human tissues. Paratarg-7 reactivity was similarly frequent among IgA and IgG paraproteins, but all paratarg-7 reactive IgG paraproteins belonged to the IgG3 subtype with 24/57 IgG3 (42.1%) paraproteins displaying this specificity. Sequence analysis of paratarg-7 derived from patients having a paraprotein with specificity for paratarg-7 revealed no differences to paratarg-7 derived from patients with paraproteins of other specificities or healthy controls, excluding mutations or polymorphisms as a reason for its autoimmunogenicity. Similarly, Western-blot analysis showed identical bands for paratarg-7 derived from patients and controls. The above-random frequency of paratarg-7 as a paraprotein target suggests that paratarg-7 might be involved in the development of the respective clonal proliferations. The identification of paratarg-7 as an antigenic target enables the more detailed analysis of tumor-host interactions in these patients and their role in the pathogenesis of MM and MGUS.

摘要

意义未明的单克隆丙种球蛋白病(MGUS)和多发性骨髓瘤(MM)副蛋白的抗原靶点可能在这些肿瘤的发病机制中起作用。我们用192例连续的MGUS和MM患者含IgA或IgG的血清筛选了一张人胎脑来源的宏阵列。192例副蛋白中有29例(15.1%)与paratarg-7发生反应,paratarg-7是一种功能未知的蛋白,在所有人体组织中均有表达。在IgA和IgG副蛋白中,paratarg-7反应性同样常见,但所有与paratarg-7反应的IgG副蛋白均属于IgG3亚型,其中24/57(42.1%)的IgG3副蛋白具有这种特异性。对具有paratarg-7特异性副蛋白的患者来源的paratarg-7进行序列分析,发现与其他特异性副蛋白患者或健康对照来源的paratarg-7没有差异,排除了突变或多态性作为其自身免疫原性的原因。同样,蛋白质印迹分析显示患者和对照来源的paratarg-7条带相同。paratarg-7作为副蛋白靶点的上述随机频率表明,paratarg-7可能参与了各自克隆增殖的发展。将paratarg-7鉴定为抗原靶点能够更详细地分析这些患者的肿瘤-宿主相互作用及其在MM和MGUS发病机制中的作用。

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