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干扰素治疗的多发性硬化症中CD26 + CD4 + T细胞计数与发作风险

CD26 + CD4 + T cell counts and attack risk in interferon-treated multiple sclerosis.

作者信息

Sellebjerg F, Ross C, Koch-Henriksen N, Sørensen P Soelberg, Frederiksen J L, Bendtzen K, Sørensen T L

机构信息

The MS Clinic, Copenhagen University Hospital, Glostrup, Denmark.

出版信息

Mult Scler. 2005 Dec;11(6):641-5. doi: 10.1191/1352458505ms1217oa.

Abstract

Biomarkers that allow the identification of patients with multiple sclerosis (MS) with an insufficient response to immunomodulatory treatment would be desirable, as currently available treatments are only incompletely efficacious. Previous studies have shown that the expression of CD25, CD26 and CCR5 on T cells is altered in patients with active MS. We studied the expression of these molecules by flow cytometry in patients followed for six months during immunomodulatory treatment. In interferon (IFN)-beta-treated patients, we found that the hazard ratio for developing an attack was 28 in patients with CD26 + CD4 + T cell counts above median, and this risk was independent of the risk conferred by neutralizing anti-IFN-beta antibodies. CD26 + CD4 + T cell counts may identify patients with MS at increased risk of attack during treatment with IFN-beta.

摘要

由于目前可用的治疗方法疗效并不完全理想,因此能够识别出对免疫调节治疗反应不足的多发性硬化症(MS)患者的生物标志物将是非常理想的。先前的研究表明,活动性MS患者T细胞上CD25、CD26和CCR5的表达会发生改变。我们通过流式细胞术研究了这些分子在接受免疫调节治疗6个月的患者中的表达情况。在接受干扰素(IFN)-β治疗的患者中,我们发现CD26 + CD4 + T细胞计数高于中位数的患者发生发作的风险比为28,并且这种风险独立于中和性抗IFN-β抗体所带来的风险。CD26 + CD4 + T细胞计数可能有助于识别接受IFN-β治疗期间发作风险增加的MS患者。

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