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炎症性肠病患者对微卫星不稳定性诱导的移码突变的反应性。

Reactivity against microsatellite instability-induced frameshift mutations in patients with inflammatory bowel disease.

作者信息

Kuehn Florian, Klar Ernst, Bliemeister Anja, Linnebacher Michael

机构信息

Florian Kuehn, Ernst Klar, Anja Bliemeister, Michael Linnebacher, Department of General, Thoracic, Vascular and Transplantation Surgery, Molecular Oncology and Immunotherapy, University of Rostock, 18057 Rostock, Germany.

出版信息

World J Gastroenterol. 2015 Jan 7;21(1):221-8. doi: 10.3748/wjg.v21.i1.221.

Abstract

AIM

To analyze the cellular immune response towards microsatellite-instability (MSI)-induced frameshift-peptides (FSPs) in patients suffering from inflammatory bowel disease (IBD) with and without thiopurine-based immunosuppressive treatment.

METHODS

Frequencies of peripheral blood T cell responses of IBD patients (n = 75) against FSPs derived from 14 microsatellite-containing candidate genes were quantified by interferon-γ enzyme-linked immunospot. T cells derived from 20 healthy individuals served as controls.

RESULTS

Significant T cell reactivities against MSI-induced FSPs were observed in 59 of 75 IBD patients (78.7%). This was significantly more as we could observe in 20 healthy controls (P = 0.001). Overall, the reactivity was significantly influenced by thiopurine treatment (P = 0.032) and duration of disease (P = 0.002) but not by duration or cumulative amount of thiopurine therapy (P = 0.476). Unexpected, 15 of 24 (62.5%) IBD patients without prior thiopurine treatment also showed increased FSP-specific immune responses (P = 0.001).

CONCLUSION

These findings propose FSPs as potential novel class of inflammation-associated antigens and this in turn may have implications for screening, diagnosis as well as clinical management of patients suffering from IBD and other inflammatory conditions.

摘要

目的

分析炎症性肠病(IBD)患者在接受和未接受硫嘌呤类免疫抑制治疗时,针对微卫星不稳定性(MSI)诱导的移码肽(FSP)的细胞免疫反应。

方法

通过干扰素-γ酶联免疫斑点法对75例IBD患者外周血T细胞对来自14个含微卫星候选基因的FSP的反应频率进行定量。来自20名健康个体的T细胞作为对照。

结果

75例IBD患者中有59例(78.7%)观察到针对MSI诱导的FSP的显著T细胞反应性。这明显多于我们在20名健康对照中观察到的情况(P = 0.001)。总体而言,反应性受硫嘌呤治疗(P = 0.032)和病程(P = 0.002)的显著影响,但不受硫嘌呤治疗的持续时间或累积剂量的影响(P = 0.476)。出乎意料的是,24例未接受过硫嘌呤治疗的IBD患者中有15例(62.5%)也表现出FSP特异性免疫反应增加(P = 0.001)。

结论

这些发现表明FSP是一类潜在的新型炎症相关抗原,这反过来可能对IBD和其他炎症性疾病患者的筛查、诊断以及临床管理产生影响。

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