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克罗恩病患者对人连接蛋白 37及其微生物模拟物的独特抗体反应。

Peculiar antibody reactivity to human connexin 37 and its microbial mimics in patients with Crohn's disease.

机构信息

Division of Gene and Cell Based Therapy, King's College London School of Medicine at King's College Hospital, London, UK.

出版信息

J Crohns Colitis. 2011 Apr;5(2):101-9. doi: 10.1016/j.crohns.2010.10.009. Epub 2010 Dec 3.

Abstract

BACKGROUND/AIMS: We found that pooled Crohn's disease (CD) sera strongly react with a human gap-junction connexin 37 (Cx37) peptide and tested for anti-Cx37 antibody reactivity in sera from CD patients and controls. We also investigated whether peptide-recognition is due to Cx37/microbial molecular mimicry.

METHODS

The PSI-BLAST program was used for Cx37(121-135)/microbial alignment. Reactivity to biotinylated human Cx37(121-135) and its microbial mimics was determined by ELISA using sera from 44 CD, 30 ulcerative colitis and 28 healthy individuals.

RESULTS

Anti-Cx37(121-135) reactivity (1/200 dilution) was present in 30/44 (68%) CD cases and persisted at 1/1000 dilution. Database search shows that Cx37(121-135) contains the -ALTAV- motif which is cross-recognized by diabetes-specific phogrin and enteroviral immunity. Testing of 9 Cx37(121-135)-microbial mimics revealed 57-68% reactivity against human enterovirus C, Lactococcus lactis, coxsackie virus A24 and B4. Anti-Cx37(121-135) was inhibited by itself or the microbial mimics. No reactivity was found against the poliovirus, rubella, and Mycobacterium tuberculosis mimics, or the beta cell phogrin autoantigen. Microbial/Cx37 reactivity was not able to differentiate CD patients from UC or healthy controls, in terms of overall prevalence and antibody titres, but microbial mimics were unable to inhibit reactivity to human Cx37 in the majority of the controls.

CONCLUSIONS

Sera from CD patients react with connexin 37 and cross-react with specific Cx37-mimicking enteroviral peptides. Microbial/self reactivity can be seen in UC and healthy controls. The lack of responses to other Cx37(121-135) microbial mimics and the inability of the reactive microbes to inhibit reactivity to self is intriguing and warrants further investigation.

摘要

背景/目的:我们发现,汇集的克罗恩病(CD)血清与人类缝隙连接连接蛋白 37(Cx37)肽强烈反应,并在 CD 患者和对照者的血清中检测抗 Cx37 抗体反应性。我们还研究了肽识别是否归因于 Cx37/微生物分子模拟。

方法

使用 PSI-BLAST 程序进行 Cx37(121-135)/微生物对齐。使用来自 44 例 CD、30 例溃疡性结肠炎和 28 例健康个体的血清通过 ELISA 测定对生物素化的人 Cx37(121-135)及其微生物模拟物的反应性。

结果

抗 Cx37(121-135)反应性(1/200 稀释度)存在于 30/44(68%)CD 病例中,并在 1/1000 稀释度时持续存在。数据库搜索显示,Cx37(121-135)包含被糖尿病特异性 phogrin 和肠病毒免疫交叉识别的 -ALTAV-基序。对 9 种 Cx37(121-135)-微生物模拟物的测试显示,对人肠道病毒 C、乳球菌乳球菌、柯萨奇病毒 A24 和 B4 的反应性为 57-68%。抗 Cx37(121-135)被自身或微生物模拟物抑制。对脊髓灰质炎病毒、风疹病毒和结核分枝杆菌模拟物或β细胞 phogrin 自身抗原无反应性。微生物/Cx37 反应性无法根据总体流行率和抗体滴度将 CD 患者与 UC 或健康对照者区分开来,但大多数对照者中,微生物模拟物无法抑制对人 Cx37 的反应性。

结论

CD 患者的血清与连接蛋白 37 反应,并与特定的 Cx37 模拟肠病毒肽交叉反应。UC 和健康对照者可见微生物/自身反应性。对其他 Cx37(121-135)微生物模拟物的反应缺失以及反应微生物无法抑制对自身的反应性令人着迷,值得进一步研究。

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