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接受重组人干扰素α-2a治疗的白塞病葡萄膜炎患者中的抗干扰素α抗体和自身抗体。

Anti-interferon alpha antibodies and autoantibodies in patients with Behçet's disease uveitis treated with recombinant human interferon alpha-2a.

作者信息

Aydinoglu-Candan Özlem, Araz-Erşan Bilge, Gul Ahmet, Badur Selim, Tugal-Tutkun Ilknur

机构信息

Istanbul Faculty of Medicine Department of Ophthalmology, Istanbul University, Istanbul Tip Fakultesi, Goz Hastaliklari A.D. Capa, Istanbul, 34093, Turkey.

出版信息

Graefes Arch Clin Exp Ophthalmol. 2015 Mar;253(3):457-65. doi: 10.1007/s00417-014-2856-3. Epub 2014 Dec 12.

Abstract

BACKGROUND

Recombinant human (rh) interferon alpha2a (IFN-α2a) therapy is successfully used for the treatment of Behçet's disease (BD) uveitis refractory to conventional immunosuppressive treatment.

PURPOSE

Our aim in this study was to investigate the frequency and clinical significance of anti-IFN-α antibodies and autoantibodies during recombinant human rhIFN-α2a therapy in patients with BD uveitis.

METHODS

This comparative, cross-sectional, serological screening study included 30 BD patients treated with rhIFN-α2a (Group 1), 29 BD patients treated with conventional immunosuppressive agents (Group 2), 29 BD patients who received only colchicine (Group 3), and 30 healthy subjects (Group 4). Anti-IFN-α-binding antibodies and autoantibodies, including anti-nuclear antibody, anti-thyroid peroxidase antibody, and anti-cardiolipin antibody, were measured in serum samples. Antibody seropositivity was compared between study groups. Retrospective clinical data were compared between antibody-positive and antibody-negative patients.

RESULTS

A significantly higher proportion of patients in Group 1 had anti-interferon-α (26.6 %) and autoantibody (30 %) seropositivity compared to the other groups. No correlation was found between seropositivity for anti-interferon-α and other autoantibodies. No significant difference was found in cumulative dose of IFN-α, duration of IFN-α therapy, time to first uveitis attack, or attack rate between anti-interferon-α antibody-positive and antibody-negative patients in Group 1. Uveitis attacks were observed in 22 % of autoantibody-positive and 71 % of autoantibody-negative patients in Group 1 (p = 0.018).

CONCLUSIONS

Patients with BD uveitis develop anti-IFN-α-binding antibodies and autoantibodies during treatment with rhIFN-α2a. While the clinical relevance of anti-IFN-α-binding antibodies remains unclear in this study, induction of autoimmunity was found to be associated with a tendency for better therapeutic response.

摘要

背景

重组人(rh)干扰素α2a(IFN-α2a)疗法已成功用于治疗对传统免疫抑制治疗无效的白塞病(BD)葡萄膜炎。

目的

本研究的目的是调查BD葡萄膜炎患者在重组人rhIFN-α2a治疗期间抗IFN-α抗体和自身抗体的出现频率及临床意义。

方法

这项比较性、横断面血清学筛查研究纳入了30例接受rhIFN-α2a治疗的BD患者(第1组)、29例接受传统免疫抑制剂治疗的BD患者(第2组)、29例仅接受秋水仙碱治疗的BD患者(第3组)和30名健康受试者(第4组)。检测血清样本中的抗IFN-α结合抗体和自身抗体,包括抗核抗体、抗甲状腺过氧化物酶抗体和抗心磷脂抗体。比较各研究组之间的抗体血清阳性率。对抗体阳性和抗体阴性患者的回顾性临床数据进行比较。

结果

与其他组相比,第1组中抗干扰素-α(26.6%)和自身抗体(30%)血清阳性的患者比例显著更高。抗干扰素-α血清阳性与其他自身抗体之间未发现相关性。在第1组中,抗干扰素-α抗体阳性和抗体阴性患者之间,IFN-α的累积剂量、IFN-α治疗持续时间、首次葡萄膜炎发作时间或发作率均未发现显著差异。在第1组中,22%的自身抗体阳性患者和71%的自身抗体阴性患者出现了葡萄膜炎发作(p = 0.018)。

结论

BD葡萄膜炎患者在rhIFN-α2a治疗期间会产生抗IFN-α结合抗体和自身抗体。虽然本研究中抗IFN-α结合抗体的临床相关性尚不清楚,但发现自身免疫的诱导与更好的治疗反应倾向有关。

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