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前沿:人类自身免疫性疾病的分子图谱

Cutting edge: molecular portrait of human autoimmune disease.

作者信息

Maas Kevin, Chan Sanny, Parker Joel, Slater Angela, Moore Jason, Olsen Nancy, Aune Thomas M

机构信息

Division of Rheumatology, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.

出版信息

J Immunol. 2002 Jul 1;169(1):5-9. doi: 10.4049/jimmunol.169.1.5.

Abstract

Autoimmune diseases affect 3-5% of the population, are mediated by the immune response to self-Ags, and are characterized by the site of tissue destruction. We compared expression levels of >4,000 genes in PBMC of control individuals before and after immunization to those of individuals with four distinct autoimmune diseases. The gene expression profile of the normal immune response exhibits coordinate changes in expression of genes with related functions over time. In contrast, each individual from all autoimmune diseases displays a similar gene expression profile unrelated to the pattern of the immunized group. To our surprise, genes with a distinct expression pattern in autoimmunity are not necessarily "immune response" genes, but are genes that encode proteins involved in apoptosis, cell cycle progression, cell differentiation, and cell migration.

摘要

自身免疫性疾病影响3%至5%的人口,由针对自身抗原的免疫反应介导,并以组织破坏部位为特征。我们比较了免疫前后对照个体外周血单核细胞(PBMC)中4000多个基因的表达水平与四种不同自身免疫性疾病患者的基因表达水平。正常免疫反应的基因表达谱显示,随着时间的推移,具有相关功能的基因表达会发生协同变化。相比之下,所有自身免疫性疾病的每个个体都表现出与免疫组模式无关的相似基因表达谱。令我们惊讶的是,在自身免疫中具有独特表达模式的基因不一定是“免疫反应”基因,而是编码参与细胞凋亡、细胞周期进程、细胞分化和细胞迁移的蛋白质的基因。

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