克罗恩病患者抗肿瘤坏死因子治疗过程中一些常规免疫参数的动态变化

T. Velikova, Z. Spassova, L. M. Milatchkov, D. Panova, E. Todorova, K. Yuzeir, E. Kurteva, D. Kyurkchiev, S. Deredjan, R. Nikolov, I. Altankova, L. M. Vladimirova
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摘要

背景:粪便和免疫生物标志物可用于克罗恩病(CD)患者的诊断和管理。除生物标志物外,还应评估抗肿瘤坏死因子(TNF)以确定对治疗的反应。目的:本研究旨在追踪CD患者粪便钙保护蛋白(FC)、核周抗中性粒细胞胞浆抗体(pANCA)、抗酵母抗体(ASCA)和抗核抗体(ANA)在抗tnf治疗中的变化。方法:对57例CD患者(平均年龄40±15岁,范围20 ~ 75岁)进行抗TNFa治疗后的监测。在开始和接受免疫抑制加抗TNFa药物治疗6个月后,对粪便样本进行FC (Alegria自动酶联免疫吸附试验(ELISA)系统)和血清样本进行ANCA、ANA(间接免疫荧光IIF)和ASCA (ELISA)检测。结果:观察到所有CD患者在抗TNFa治疗后FC水平显著降低(最初为963.97 mg/kg,治疗后为268.42 mg/kg;P = 0.043)。此外,在75%的患者中,FC水平降至50mg /kg的临界值以下。ASCA IgA/IgG阳性的患者有17/24,但在抗tnf治疗的应用方面没有观察到差异。然而,抗tnf治疗后,4例患者的pANCA滴度下降。结论:初始和随访测量一些免疫标志物,如FC和pANCA,可能对CD患者抗TNF治疗有益,而其他如ANA和ASCA,对监测治疗无效。
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Dynamics of Some Routine Immunological Parameters During Anti - TNF Therapy in Patients with Crohn’s Disease
Background: Fecal and immunological biomarkers can be used to diagnose and manage patients with Crohn’s disease (CD). Anti tumor necrosis factor (TNF) should be evaluated in addition to biomarkers to determine the response to therapy. Objectives: The current study aimed at following up fecal calprotectin (FC), perinuclear anti neutrophil cytoplasmic antibodies (pANCA), anti Saccharomyces cerevisiae antibodies (ASCA), and anti nuclear antibodies (ANA) in patients with CD on anti-TNF therapy. Methods: A total of 57 patients with CD and the mean age of 40 ± 15 years (ranged: 20 75) were monitored after initiation of anti TNFa treatment. Stool samples were tested for FC (Alegria automated the enzyme linked immunosorbent assay (ELISA) system), and serum samples for ANCA, ANA (indirect immunofluorescence IIF), and ASCA (ELISA) in the beginning and after six months on immunosuppressive therapy plus anti TNFa agents. Results: It was observed that all patients with CD had significantly decreased FC levels after anti TNFa therapy (963.97 mg/kg initially vs. 268.42 mg/kg after treatment; P = 0.043). Moreover, in 75% of patients, FC levels dropped below the cutoff value of 50 mg/kg. Positive for ASCA IgA/IgG were 17/24 tested patients, but no differences were observed regarding the application of anti TNFa therapy. However, the titers of pANCA decreased in four patients after anti TNFa treatment. Conclusions: Initial and follow up measurements of some immunological markers such as FC and pANCA could be of benefit for patients with CD in anti TNF therapy, whereas others such as ANA and ASCA were not useful to monitor the therapy.
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