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干扰素-β特异性 T 细胞与干扰素-β治疗多发性硬化症患者中中和抗体的产生有关。

Interferon-beta specific T cells are associated with the development of neutralizing antibodies in interferon-beta treated multiple sclerosis patients.

机构信息

Klinikum rechts der Isar, Department of Neurology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany.

Klinikum rechts der Isar, Department of Neurology, School of Medicine, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.

出版信息

J Autoimmun. 2018 Mar;88:83-90. doi: 10.1016/j.jaut.2017.10.003. Epub 2017 Oct 21.

Abstract

Beta-interferons are still among the most commonly used drugs to treat Multiple Sclerosis (MS). The use of beta-interferons is limited by the development of anti-drug antibodies (ADA), which may abrogate the treatment effect of the drug. Although the antibody response has been well studied, little is known about the T cell response to interferon-beta (IFN-β). We investigated T cell responses in four treatment naïve MS patients and twenty-three patients treated with IFN-β who had or had not developed ADA to IFN-β. T cell responses were determined by split-well and primary proliferation assays against different IFN-β protein preparations and a set of overlapping peptides covering the full sequence of IFN-β. T cell responses to IFN-β were observed in all donors. ADA positive patients showed higher T cell responses to IFN-β protein than ADA negative patients and untreated controls. We identified two immunodominant regions; T cell responses to IFN-β were observed in all patients independent of ADA status, while T cell responses to IFN-β were stronger in ADA positive than ADA negative patients. IFN-β specific T cell responses were HLA class II restricted and in ADA positive patients skewed towards a Th2 phenotype. In IFN-β treated patients we observed a correlation between IFN-β specific T cell responses, serum ADA titer and loss of biological activity of IFN-β treatment. Our studies demonstrate the occurrence of an antigen specific HLA class II restricted Th2 T cell response associated with the development of ADA in IFN-β treated patients.

摘要

β干扰素仍是治疗多发性硬化症(MS)最常用的药物之一。由于药物抗体(ADA)的产生,β干扰素的使用受到限制,这可能会消除药物的治疗效果。尽管已经对抗体反应进行了广泛研究,但对于干扰素-β(IFN-β)的 T 细胞反应知之甚少。我们在四名未经治疗的 MS 患者和 23 名接受 IFN-β治疗的患者中进行了研究,这些患者中有或没有产生针对 IFN-β的 ADA。通过分裂孔和针对不同 IFN-β蛋白制剂和一组覆盖 IFN-β全长序列的重叠肽的原发性增殖测定来确定 T 细胞反应。在所有供体中均观察到对 IFN-β的 T 细胞反应。ADA 阳性患者对 IFN-β蛋白的 T 细胞反应高于 ADA 阴性患者和未治疗的对照组。我们确定了两个免疫优势区域;所有患者均观察到对 IFN-β的 T 细胞反应,而与 ADA 状态无关,而 ADA 阳性患者的 IFN-β特异性 T 细胞反应强于 ADA 阴性患者。IFN-β特异性 T 细胞反应受到 HLA Ⅱ类限制,在 ADA 阳性患者中向 Th2 表型倾斜。在 IFN-β治疗的患者中,我们观察到 IFN-β特异性 T 细胞反应、血清 ADA 滴度和 IFN-β治疗生物活性丧失之间存在相关性。我们的研究表明,在 IFN-β治疗的患者中,存在与 ADA 发展相关的抗原特异性 HLA Ⅱ类限制的 Th2 T 细胞反应。

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