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多发性硬化症患者中针对干扰素-β的抗体交叉反应及 JAK-STAT 信号通路的干扰。

Cross-reactivity of antibodies against interferon beta in multiple sclerosis patients and interference of the JAK-STAT signaling pathway.

机构信息

Unidad de Gestión Clínica de Neurociencias, Instituto de Biomedicina de Málaga (IBIMA), Hospital Regional Universitario de Málaga, Universidad de Málaga, Málaga, Spain.

Red Española de Esclerosis Multiple (REEM), Instituto de Salud Carlos III, Madrid, Spain.

出版信息

Sci Rep. 2017 Nov 29;7(1):16585. doi: 10.1038/s41598-017-16828-x.

Abstract

Interferon beta (IFNβ) therapy has immunogenic properties and induces the development of neutralizing antibodies (NAbs). From the extensive literature focused in the development of NAbs in multiple sclerosis (MS) patients, their ability to cross-react has been deficiently evaluated, despite having important consequences in the clinical practice. Here, the relation between the cross-reactivity and the NAbs titers has been evaluated in MS patients, by inhibition of the antiviral activity of IFNβ by bioassay and through the interference with the activation of the IFNß pathway (JAK-STAT), by phosphoflow. Thus, patients with intermediate-high titers of NAbs, determined by bioassay, had a 79-fold increased risk of cross-reactivity compared to patients with low titers. The cross-reactivity is also demonstrated because NAbs positive sera were able to decrease significantly the activation of pSTAT1 achieved by other different IFNβ molecules in the cells patients. Besides, a linear relationship between the STAT1 phosphorylation and NAbs titers was found. The study demonstrates that cross-reactivity increases with the titer of antibodies, which has important implications in clinical practice when switching the treatment. The direct relationship between the NAbs titer and the activation of STAT1 suggest that its determination could be an indirect method to identify the presence of NAbs.

摘要

干扰素β(IFNβ)治疗具有免疫原性,并诱导中和抗体(NAbs)的产生。从大量专注于多发性硬化症(MS)患者 NAbs 发展的文献中可以看出,尽管在临床实践中有重要影响,但对其交叉反应能力的评估还不够充分。在这里,通过生物测定法抑制 IFNβ 的抗病毒活性,并通过磷酸化流式细胞术干扰 IFNβ 途径(JAK-STAT)的激活,评估了 MS 患者中交叉反应性与 NAbs 滴度之间的关系。因此,与低滴度的患者相比,生物测定法测定的中高滴度 NAbs 的患者发生交叉反应的风险增加了 79 倍。交叉反应性也得到了证明,因为 NAbs 阳性血清能够显著降低患者细胞中其他不同 IFNβ 分子诱导的 pSTAT1 激活。此外,还发现 STAT1 磷酸化与 NAbs 滴度之间存在线性关系。该研究表明,交叉反应性随抗体滴度的增加而增加,这在治疗转换时具有重要的临床意义。NAbs 滴度与 STAT1 激活之间的直接关系表明,其测定可能是识别 NAbs 存在的间接方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e97/5707350/b9f2ebc2ddce/41598_2017_16828_Fig1_HTML.jpg

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