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SmD分子上抗原表位的定位:利用多抗原肽检测系统性红斑狼疮中的自身抗体。

Mapping of epitopes on the SmD molecule: the use of multiple antigen peptides to measure autoantibodies in systemic lupus erythematosus.

作者信息

Sabbatini A, Dolcher M P, Marchini B, Bombardieri S, Migliorini P

机构信息

Clinical Immunology Unit, University of Pisa, Italy.

出版信息

J Rheumatol. 1993 Oct;20(10):1679-83.

PMID:7507527
Abstract

Autoantibodies against the ribonucleoproteins B, B' and D are a serological marker of systemic lupus erythematosus (SLE). We mapped the epitopes recognized by autoantibodies on the SmD molecule by means of 7 synthetic peptides corresponding to the entire length of the protein. By ELISA assay, 25% of the lupus sera contained IgG antibodies specific for the C-terminal SmD sequence 95-119. This reactivity was confirmed by synthesizing the sequence as a multiple antigen peptide (MAP): antibodies reactive with the MAP 95-119 were present only in SLE and not in other connective tissue disorders. Sera containing high titers of anti-MAP 95-119 antibodies reacted in immunoblot with the SmD protein. These results indicate the presence of a dominant epitope in the C-terminal region of SmD, which is highly homologous to the Epstein-Barr virus induced nuclear protein EBNA I.

摘要

针对核糖核蛋白B、B' 和D的自身抗体是系统性红斑狼疮(SLE)的血清学标志物。我们借助7种与该蛋白全长对应的合成肽,绘制了自身抗体在SmD分子上识别的表位。通过ELISA检测,25% 的狼疮血清含有对C端SmD序列95 - 119特异的IgG抗体。通过将该序列合成为多抗原肽(MAP)证实了这种反应性:与MAP 95 - 119反应的抗体仅存在于SLE患者血清中,而不存在于其他结缔组织疾病患者血清中。含有高滴度抗MAP 95 - 119抗体的血清在免疫印迹中与SmD蛋白发生反应。这些结果表明SmD的C端区域存在一个显性表位,它与爱泼斯坦 - 巴尔病毒诱导的核蛋白EBNA I高度同源。

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