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首页> 外文期刊>Inflammatory bowel diseases >Specific antibodies against recombinant protein of insertion element 900 of Mycobacterium avium subspecies paratuberculosis in Japanese patients with Crohn's disease.
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Specific antibodies against recombinant protein of insertion element 900 of Mycobacterium avium subspecies paratuberculosis in Japanese patients with Crohn's disease.

机译:在日本克罗恩氏病患者中,抗鸟分枝杆菌亚种副结核菌插入元件900重组蛋白的特异性抗体。

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摘要

BACKGROUND: Mycobacterial avium subspecies paratuberculosis (MAP) infection has been hypothesized as an etiological factor of Crohn's disease (CD). However, the involvement of MAP in the pathophysiology of CD is controversial. The aim of this study is to investigate whether MAP is involved in the pathogenesis of CD with the glutathione S-transferase fusion recombinant protein encoding a portion of insertion element (IS) 900 (IS900-GST), which is specific for MAP. METHODS: Serum samples from the patients with CD (n = 50), ulcerative colitis (n = 40), colonic tuberculosis (n = 20), and non-IBD controls (n = 44), were applied for solid-phase enzyme-linked immunosorbent assay (ELISA) to detect antibodies against MAP and Saccharomyces cerevisiae. IS900-GST, which was made by the pGST-4T-2 vector inserted with polymerase chain reaction-amplified IS900DNA, was used as an antigen of MAP. Moreover, we studied the relationship between antibodies against IS900-GST and clinical characteristics. RESULTS: ELISA showed that the serum level of immunoglobulin G and immunoglobulin A antibodies against IS900-GST (anti-IS900) in patients with CD were significantly higher than those with ulcerative colitis, colonic tuberculosis, and control subjects. The levels of anti-IS900 tended to be higher in CD patients with small intestinal involvement than with colonic involvement alone. Anti-IS900 in patients with penetrating- and stricture-type CD was significantly higher than with inflammatory-type CD. Furthermore, a negative correlation was found between the titer of anti-IS900 and disease duration. Anti-IS900 was not associated with surgical treatment nor was it associated with the use of immunosuppressants. No significant correlation was observed between the serum levels of anti-IS900 and anti-S cerevisiae antibody. CONCLUSIONS: This is the first demonstration of the ELISA system of detecting antibodies against IS900 in IBD patients. MAP could be involved in the pathophysiology of Japanese patients with CD.
机译:背景:结核分枝杆菌亚种副结核病(MAP)感染被假定为克罗恩病(CD)的病因。然而,MAP参与CD的病理生理学是有争议的。这项研究的目的是研究谷胱甘肽S-转移酶融合重组蛋白编码的一部分插入元件(IS)900(IS900-GST),这对于MAP而言,MAP是否参与CD的发病机理。方法:将CD患者(n = 50),溃疡性结肠炎(n = 40),结肠结核(n = 20)和非IBD对照(n = 44)患者的血清样本用于固相酶连接免疫吸附测定(ELISA)来检测针对MAP和啤酒酵母的抗体。将通过插入聚合酶链反应扩增的IS900DNA的pGST-4T-2载体制成的IS900-GST用作MAP的抗原。此外,我们研究了针对IS900-GST的抗体与临床特征之间的关系。结果:ELISA显示,CD患者的抗IS900-GST(抗IS900)免疫球蛋白G和免疫球蛋白A抗体的水平显着高于溃疡性结肠炎,结肠结核和对照人群。在小肠受累的CD患者中,抗IS900的水平往往高于仅结肠受累的CD患者。穿透型和狭窄型CD患者的抗IS900显着高于炎症型CD患者。此外,在抗IS900的效价和疾病持续时间之间发现负相关。抗IS900与手术治疗无关,也与免疫抑制剂的使用无关。抗IS900和抗S啤酒酵母的血清水平之间没有观察到显着相关性。结论:这是用于检测IBD患者中抗IS900抗体的ELISA系统的首次证明。 MAP可能与日本CD患者的病理生理有关。

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