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分子克隆揭示近半数克罗恩病患者存在针对过氧化物还原酶 6 样蛋白的抗体。

Molecular cloning reveals nearly half of patients with Crohn's disease have an antibody to peroxiredoxin 6-like protein.

机构信息

Akita Health Care Center, Akita Red Cross Hospital, Akita University School of Medicine, Akita, Japan.

出版信息

J Gastroenterol Hepatol. 2012 Aug;27(8):1388-94. doi: 10.1111/j.1440-1746.2012.07147.x.

Abstract

BACKGROUND AND AIM

Crohn's disease (CD) is a chronic inflammatory bowel disease (IBD) of unknown etiology. We aimed to identify the etiological agent of CD using a molecular cloning strategy that was particularly focused on identifying agents causing immune abnormalities and infectious agents.

METHODS

We constructed a cDNA library derived from the inflamed intestinal tissue of a CD patient, and screened 1.5 million clones in this library with the serum from another typical CD patient. The expressed cDNA clones that positively reacted with the serum were then expressed as fusion proteins with glutathione S-transferase, and western blotting was performed using the sera of 22 CD, 13 ulcerative colitis (UC), and 16 non-IBD patients.

RESULTS

We identified nine positive clones that did not contain any viral or bacterial genomic DNA. Of these, we selected one clone (clone 50) with which the typical CD patient's serum most strongly reacted. Clone 50 is highly homologous to the antioxidant protein peroxiredoxin 6. In western blotting, the sera of 47.6% CD patients (small intestine type 80%, large and small intestine type 43%, large intestine type 0%) showed strong reactivity to clone 50, none of the UC patients were reactive to clone 50, and 18.8% of non-IBD patients were very weakly reactive to it. We also found that the expression of peroxiredoxin 6 was significantly increased in inflamed intestinal epithelia of CD.

CONCLUSION

The present study first showed that some CD patients have an antibody against peroxiredoxin 6-like protein, which may be involved in the pathogenesis of CD.

摘要

背景与目的

克罗恩病(CD)是一种病因不明的慢性炎症性肠病(IBD)。我们旨在使用特别侧重于识别引起免疫异常和感染因子的病因的分子克隆策略来鉴定 CD 的病因因子。

方法

我们构建了源自 CD 患者炎症性肠组织的 cDNA 文库,并使用另一位典型 CD 患者的血清在该文库中筛选了 150 万个克隆。与血清呈阳性反应的表达 cDNA 克隆随后被表达为与谷胱甘肽 S-转移酶融合的蛋白,并使用 22 例 CD、13 例溃疡性结肠炎(UC)和 16 例非 IBD 患者的血清进行 Western 印迹分析。

结果

我们鉴定了九个未包含任何病毒或细菌基因组 DNA 的阳性克隆。其中,我们选择了一个与典型 CD 患者血清反应最强的克隆(克隆 50)。克隆 50 与抗氧化蛋白过氧化物酶 6 高度同源。在 Western 印迹中,47.6%的 CD 患者(小肠型 80%,大小肠型 43%,大肠型 0%)的血清对克隆 50 表现出强烈的反应性,UC 患者无一例对克隆 50 反应,18.8%的非 IBD 患者对其反应非常弱。我们还发现过氧化物酶 6 的表达在 CD 的炎症性肠上皮中显著增加。

结论

本研究首次表明,一些 CD 患者存在针对过氧化物酶 6 样蛋白的抗体,这可能与 CD 的发病机制有关。

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