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在常规临床实验室中,将BAb和MxA作为功能生物标志物,用于测定多发性硬化症患者体内的抗IFN-β抗体及其生物活性水平。

BAb and MxA as functional biomarkers in routine clinical laboratories for the determination of anti-IFN-beta antibodies and their bioactivity levels in multiple sclerosis patients.

作者信息

Cakal Bulent, Uygunoglu Ugur, Saip Sabahattin, Altintas Ayse, Siva Aksel, Badur Selim

机构信息

a Department of Microbiology and Clinical Microbiology, Istanbul Medical Faculty , Istanbul University , Istanbul , Turkey.

出版信息

J Immunoassay Immunochem. 2014;35(4):398-411. doi: 10.1080/15321819.2014.885447.

Abstract

In MS patients under IFNβ treatment to seek alternative treatments timely is important that anti-IFNβ antibodies and/or in vivo biologic activity loss detection in these. The most common diagnostic markers used for this purpose are BAb, Nab, and MxA. In this article, we aimed to establish the availability and feasibility of the correlation between BAb and MxA gene expression (mRNA) levels using evaluation of responses to IFNβ treatment for MS patients with a routine laboratory follow-up strategy in a major Turkish MS center. Bab seropositivity was determined in blood samples of 218 MS patients treated with different IFNβ preparations and MxA mRNA levels were measured in 128 patients among the total population. BAb seropositivity ratios to im INF-β 1a, scINF-β 1a, and sc INF-β 1b were 21.4%, 28.6%, and 70.4%, respectively (total 40%), and total loss of bioactivity (MxA mRNA) were 9.3%, 9.5%, and 11.6%, respectively (total 10.2%). The correlation between high BAb titers and low MxA mRNA levels was highly significant (P = 0.00003). Our data indicate that there is a good correlation between especially high BAbs levels and diminished MxA mRNA levels.

摘要

在接受干扰素β治疗的多发性硬化症患者中,及时寻求替代治疗很重要,这涉及检测这些患者体内的抗干扰素β抗体和/或生物活性丧失情况。用于此目的的最常见诊断标志物是BAb、Nab和Mx A。在本文中,我们旨在通过在土耳其一家主要的多发性硬化症中心采用常规实验室随访策略评估多发性硬化症患者对干扰素β治疗的反应,来确定BAb与Mx A基因表达(mRNA)水平之间相关性的可用性和可行性。在218例接受不同干扰素β制剂治疗的多发性硬化症患者的血液样本中测定了BAb血清阳性率,并在总人群中的128例患者中测量了Mx A mRNA水平。对肌内注射干扰素β-1a、皮下注射干扰素β-1a和皮下注射干扰素β-1b的BAb血清阳性率分别为21.4%、28.6%和70.4%(总计40%),生物活性完全丧失(Mx A mRNA)的比例分别为9.3%、9.5%和11.6%(总计10.2%)。高BAb滴度与低Mx A mRNA水平之间的相关性非常显著(P = 0.00003)。我们的数据表明,尤其是高BAb水平与降低的Mx A mRNA水平之间存在良好的相关性。

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