Gibbs Ebrima, Oger Joel
Neuro-Immunology Laboratory, Department of Medicine, University of British Columbia, 2211 Wesbrook Mall, Vancouver, BC, Canada.
J Neuroimmunol. 2007 Oct;190(1-2):146-50. doi: 10.1016/j.jneuroim.2007.07.022. Epub 2007 Sep 7.
Anti-Interferon beta (IFNbeta) antibodies are frequently produced during treatment with IFNbeta in Multiple Sclerosis (MS) patients. In recent years, it has become clear that these antibodies cause a decrease in IFNbeta-induced biomarkers and in IFNbeta clinical efficacy. Anti-IFNbeta antibodies are mainly of the IgG isotype, which consists of 4 subclasses. In this study, we tested whether changes occurred in IgG subclasses over time. A series of sera from 21 IFNbeta-treated patients (11 IFNbeta-1a, 10 IFNbeta-1b) were analysed longitudinally using a capture ELISA. IFNbeta-1a treated patients had a restricted subclass distribution, whilst IFNbeta-1b-treated patients demonstrated a wider distribution. When compared to IFNbeta-1b-treated patients, IFNbeta-1a-treated patients had lower levels of total and subclass-specific IgGs against IFNbeta. In particular, antibody levels were markedly lower in the neutralizing antibody (NAb) negative (-) category of IFNbeta-1a-treated patients in comparison to the NAb-IFNbeta-1b-treated patients. The most striking observation of this study were the very low levels or complete absence of IgG3 subclass-specific antibodies to IFNbeta in IFNbeta-1a-treated patients. This difference in the levels of IgG3 may help to clarify the differences in the overall pattern of development of anti-IFNbeta antibodies in IFNbeta-1a-and IFNbeta-1b-treated patients.
在多发性硬化症(MS)患者接受β-干扰素(IFNβ)治疗期间,经常会产生抗IFNβ抗体。近年来,已经明确这些抗体导致IFNβ诱导的生物标志物减少以及IFNβ临床疗效降低。抗IFNβ抗体主要为IgG同种型,其由4个亚类组成。在本研究中,我们测试了IgG亚类是否随时间发生变化。使用捕获ELISA对21例接受IFNβ治疗的患者(11例IFNβ-1a,10例IFNβ-1b)的一系列血清进行纵向分析。接受IFNβ-1a治疗的患者亚类分布受限,而接受IFNβ-1b治疗的患者亚类分布较广。与接受IFNβ-1b治疗的患者相比,接受IFNβ-1a治疗的患者针对IFNβ的总IgG和亚类特异性IgG水平较低。特别是,与接受IFNβ-1b治疗的患者相比,接受IFNβ-1a治疗的患者中中和抗体(NAb)阴性(-)类别中的抗体水平明显较低。本研究最显著的观察结果是接受IFNβ-1a治疗的患者中针对IFNβ的IgG3亚类特异性抗体水平极低或完全缺失。IgG3水平的这种差异可能有助于阐明接受IFNβ-1a和IFNβ-1b治疗的患者中抗IFNβ抗体总体发展模式的差异。