Doronin Visilii B, Parkhomenko Taisiya A, Castellazzi Massimiliano, Padroni Marina, Pastore Michela, Buneva Valentina N, Granieri Enrico, Nevinsky Georgy A
Novosibirsk Medical University, Ministry of Public Health of Russian Federation, Novosibirsk, Russia.
Institute of Chemical Biology and Fundamental Medicine, Russian Academy of Sciences, Siberian Division, Novosibirsk, Russia.
PLoS One. 2014 Sep 29;9(9):e107807. doi: 10.1371/journal.pone.0107807. eCollection 2014.
It was found that antibodies (Abs) against myelin basic protein (MBP) are the major components of the antibody response in multiple sclerosis (MS) patients. We have recently shown that IgGs from sera of MS patients are active in the hydrolysis of MBP. However, in literature there are no available data concerning possible MBP-hydrolyzing Abs in cerebrospinal fluid (CSF) of MS patients. We have shown that the average content of IgGs in their sera is about 195-fold higher than that in their CSF. Here we have compared, for the first time, the average content of lambda- and kappa-IgGs as well as IgGs of four different subclasses (IgG1-IgG4) in CSF and sera of MS patients. The average relative content of lambda-IgGs and kappa -IgGs in the case of CSFs (8.0 and 92.0%) and sera (12.3 and 87.7%) are comparable, while IgG1, IgG2, IgG3, and IgG4: CSF - 40.4, 49.0, 8.2, and 2.5% of total IgGs, respectively and the sera - 53.6, 36.0, 5.6, and 4.8%, decreased in different order. Electrophoretically and immunologically homogeneous IgGs were obtained by sequential affinity chromatography of the CSF proteins on protein G-Sepharose and FPLC gel filtration. We present first evidence showing that IgGs from CSF efficiently hydrolyze MBP and that their average specific catalytic activity is unpredictably ∼54-fold higher than that of Abs from sera of the same MS patients. Some possible reasons of these findings are discussed. We suggest that anti-MBP abzymes of CSF may promote important neuropathologic mechanisms in this chronic inflammatory disorder and in MS pathogenesis development.
研究发现,抗髓鞘碱性蛋白(MBP)抗体(Abs)是多发性硬化症(MS)患者抗体反应的主要成分。我们最近发现,MS患者血清中的IgG对MBP具有水解活性。然而,关于MS患者脑脊液(CSF)中可能存在的MBP水解抗体,文献中尚无可用数据。我们已经表明,他们血清中IgG的平均含量比脑脊液中的高约195倍。在此,我们首次比较了MS患者脑脊液和血清中λ-和κ-IgG以及四种不同亚类(IgG1-IgG4)IgG的平均含量。脑脊液中λ-IgG和κ-IgG的平均相对含量(分别为8.0%和92.0%)与血清中的(分别为12.3%和87.7%)具有可比性,而IgG1、IgG2、IgG3和IgG4:脑脊液中分别占总IgG的40.4%、49.0%、8.2%和2.5%,血清中分别为53.6%、36.0%、5.6%和4.8%,其含量以不同顺序降低。通过蛋白G-琼脂糖凝胶亲和层析和FPLC凝胶过滤对脑脊液蛋白进行连续分离,获得了电泳和免疫均一的IgG。我们首次提供证据表明,脑脊液中的IgG能够有效水解MBP,并且其平均比催化活性比同一MS患者血清中的抗体高出约54倍,这一结果出人意料。本文讨论了这些发现的一些可能原因。我们认为,脑脊液中的抗MBP抗体酶可能在这种慢性炎症性疾病以及MS发病机制中促进重要的神经病理机制。