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内质网氨肽酶-1(ERAP-1)与家族性地中海热(FMF)的关联。

The association of endoplasmic reticulum aminopeptidase-1 (ERAP-1) with Familial Mediterranean Fever (FMF).

机构信息

Department of Internal Medicine, Maltepe University Faculty of Medicine, Istanbul, Turkey.

Department of Family Medicine, Kartal Lutfu Kirdar Training and Research Hospital, Istanbul, Turkey.

出版信息

United European Gastroenterol J. 2016 Feb;4(1):92-6. doi: 10.1177/2050640615584536. Epub 2015 May 5.

Abstract

BACKGROUND

The ERAP1 gene cleaves the receptors and reduces their ability to transmit chemical signals to the cell that affect the process of inflammation and, secondly, it cleaves many types of proteins into small peptides that are recognized by the immune system.

OBJECTIVE

ERAP-1 gene mutations may create a sensitivity for Familial Mediterranean Fever (FMF).

METHOD

We included 15 FMF patients with the M694 (+) mutation in the study in order to exclude patients without pyrin gene mutations and create a homogeneous study group. Fifteen patients with ulcerative colitis formed the control group.

RESULTS

There wasn't any case without ERAP-1 gene mutations. At least one mutation at exon 3 or exon 10 was found in all cases in both groups. There were 14 ERAP-1 gene mutations at exon 10 and 11 at exon 3 in patients with FMF. Interestingly, if there were ERAP-1 gene mutations at exon 3, a p.Arg127 Pro (c.380 G>C) mutation always existed for three FMF patients with polymorphic mutations at this exon. There were 11 ERAP-1 gene mutations at exon 10 and 12 gene mutations at exon 3 in patients with ulcerative colitis. Exon 3 mutations were usually single p.Arg127 Pro (c.380 G>C) mutations for 12 patients with ulcerative colitis as seen in the patients with FMF. The single mutation was always p.Ser453 Ser (c.1359T>C) for patients with ulcerative colitis at exon 10.

CONCLUSION

There are more ERAP-1 mutations in the FMF group in comparison to the ulcerative colitis group. So, there may be a strong susceptibility to ERAP-1 gene mutations in FMF patients according to our results. However, further studies with larger study and control groups are needed.

摘要

背景

ERAP1 基因可切割受体,降低其向细胞传递影响炎症过程的化学信号的能力;其次,它可将多种蛋白质切割成小肽,这些小肽被免疫系统识别。

目的

ERAP-1 基因突变可能使家族性地中海热(FMF)患者敏感。

方法

我们纳入了 15 名携带 M694(+)突变的 FMF 患者,以排除无 pyrin 基因突变的患者并创建一个同质研究组。15 名溃疡性结肠炎患者作为对照组。

结果

在两个组中,所有病例均存在 ERAP-1 基因突变,至少在第 3 或第 10 外显子中存在一个突变。FMF 患者中有 14 个 ERAP-1 基因突变位于第 10 外显子,3 个位于第 3 外显子。有趣的是,如果第 3 外显子存在 ERAP-1 基因突变,则 3 例多态性突变的 FMF 患者中总会存在一个 p.Arg127 Pro(c.380 G>C)突变。溃疡性结肠炎患者中有 11 个 ERAP-1 基因突变位于第 10 外显子,3 个位于第 3 外显子。溃疡性结肠炎患者的第 3 外显子突变通常为单个 p.Arg127 Pro(c.380 G>C)突变,与 FMF 患者一样。溃疡性结肠炎患者的第 10 外显子突变通常为单个 p.Ser453 Ser(c.1359T>C)突变。

结论

FMF 组中的 ERAP-1 突变多于溃疡性结肠炎组。因此,根据我们的结果,FMF 患者可能对 ERAP-1 基因突变有较强的易感性。然而,需要进一步进行具有更大研究和对照组的研究。

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