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血清抗体在鉴别炎症性肠病、预测新诊断患者的疾病活动度和病程中的价值。

The value of serum antibodies in differentiating inflammatory bowel disease, predicting disease activity and disease course in the newly diagnosed patient.

作者信息

Smids Carolijn, Horjus Talabur Horje Carmen S, Groenen Marcel J M, van Koolwijk Elly H M, Wahab Peter J, van Lochem Ellen G

机构信息

a Crohn & Colitis Centre Rijnstate, Department of Gastroenterology and Hepatology , Rijnstate Hospital , Arnhem , The Netherlands.

b Department of Microbiology and Immunology , Rijnstate Hospital , Arnhem , The Netherlands.

出版信息

Scand J Gastroenterol. 2017 Oct;52(10):1104-1112. doi: 10.1080/00365521.2017.1344875. Epub 2017 Jun 29.

Abstract

BACKGROUND

Data on serum antibodies in untreated adult inflammatory bowel disease (IBD) patients at diagnosis are scarcely available, and results on the stability of antibody presence over time are inconsistent. Our aim was to investigate antibodies in newly diagnosed, untreated IBD patients in relation to disease phenotype and course. Furthermore, we analyzed antibody presence over time.

METHODS

Baseline anti-Saccharomyces cerevisiae antibodies (ASCA), anti-chitobioside carbohydrate antibodies (ACCA), anti-laminaribioside carbohydrate antibodies (ALCA) and anti-mannobioside carbohydrate antibodies (AMCA) were measured with enzyme-linked immunosorbent assays and perinuclear anti-neutrophilic cytoplasmic antibodies (pANCA) was measured by indirect immunofluorescence in serum of 120 untreated IBD patients at diagnosis and 19 healthy controls. Antibodies were related to disease outcomes. Serial measurements were available in 71 patients.

RESULTS

The combination of pANCA and ASCA enabled good discrimination between UC and CD (p = .004). Antibody presence was relatively stable over time, even though there were significant changes in concentrations. There was a trend towards larger fluctuations in concentration with immunosuppressive medication. Baseline pANCA in UC patients correlated with calprotectin values (rho = .545, p = .019) and change in pANCA status over time was associated with disease activity at that moment. No associations were found with antibodies at diagnosis and disease outcomes.

CONCLUSION

Antibody profiles at diagnosis support the distinction between CD and UC. Anti-glycan antibodies are reasonably stable over time, but may fluctuate under the influence of immunosuppressive treatment which may explain the inconsistency in findings hitherto. The appearance or disappearance of pANCA antibodies during follow-up correlated with disease activity in UC and may be used in disease monitoring.

摘要

背景

关于未经治疗的成年炎症性肠病(IBD)患者诊断时血清抗体的数据很少,并且关于抗体随时间存在的稳定性结果也不一致。我们的目的是研究新诊断的、未经治疗的IBD患者中与疾病表型和病程相关的抗体。此外,我们分析了抗体随时间的存在情况。

方法

采用酶联免疫吸附测定法检测120例未经治疗的IBD患者诊断时血清中的抗酿酒酵母抗体(ASCA)、抗壳二糖苷碳水化合物抗体(ACCA)、抗层粘连二糖苷碳水化合物抗体(ALCA)和抗甘露二糖苷碳水化合物抗体(AMCA),并通过间接免疫荧光法检测核周抗中性粒细胞胞浆抗体(pANCA),同时检测19例健康对照者。将抗体与疾病结局相关联。71例患者有连续测量数据。

结果

pANCA和ASCA的联合检测能够很好地区分UC和CD(p = 0.004)。尽管抗体浓度有显著变化,但抗体的存在随时间相对稳定。使用免疫抑制药物时,浓度波动有增大的趋势。UC患者的基线pANCA与钙卫蛋白值相关(rho = 0.545,p = 0.019),pANCA状态随时间的变化与当时的疾病活动相关。未发现诊断时的抗体与疾病结局之间存在关联。

结论

诊断时的抗体谱有助于区分CD和UC。抗聚糖抗体随时间相当稳定,但可能在免疫抑制治疗的影响下波动,这可能解释了迄今为止研究结果的不一致性。随访期间pANCA抗体的出现或消失与UC的疾病活动相关,可用于疾病监测。

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