Department of Neurology, Dartmouth Hitchcock Medical Center (DHMC), Geisel School of Medicine, Lebanon, NH, USA.
Department of Neurology, Dartmouth Hitchcock Medical Center (DHMC), Geisel School of Medicine, Lebanon, NH, USA.
Int Immunopharmacol. 2018 Sep;62:1-6. doi: 10.1016/j.intimp.2018.06.030. Epub 2018 Jun 27.
Because PEGylated molecules exhibit different physicochemical properties from those of the parent molecules, PEGylated interferonβ-1a (pegIFNβ-1a) may be able to be used with retained bioactivity in Multiple Sclerosis (MS) patients who have previously developed neutralizing antibodies (NABs) to recombinant interferonβ (rIFNβ). Hence, the objective of the present study was to test whether pegIFNβ-1a is less antigenic for NABs in vitro than rIFNβ. Two in vitro assays were used to quantitate NABs in 115 sera obtained from MS patients included in the INSIGHT study: the cytopathic effect (CPE) assay, and the MxA protein induction assay. NABs cross-reactivity was assessed by comparing dilutions of serum with fixed doses of rIFNβ-1a Avonex® and pegIFNβ-1a Plegridy®. NABs were shown to cross-react in both assays. The y-intercept (c), the slope of the line of agreement (b), the Pearson coefficients as well as the Bland-Altman analysis, indicated that there is good level of agreement between NAB titers against the two IFNβ-1a formulations, with both the CPE (c = 0.1044 ± 0.1305; b = 0.8438 ± 0.06654; r = 0.587; bias index ± SD = -0.01702 ± 0.6334), and the MxA protein induction (c = 0.08246 ± 0.1229; b = 0.8878 ± 0.06613; r = 0.615; bias index ± SD = -0.09965 ± 0.6467) assays. Until further in vivo evidence is established, clinicians should consider the current in vitro data demonstrating NAB cross-reactivity between pegIFNβ-1a and rIFNβ when discussing new treatment options with MS patients.
由于聚乙二醇化分子表现出与母体分子不同的物理化学性质,因此在先前对重组干扰素β(rIFNβ)产生中和抗体(NABs)的多发性硬化症(MS)患者中,聚乙二醇化干扰素β-1a(pegIFNβ-1a)可能能够保持生物活性而被使用。因此,本研究的目的是测试 pegIFNβ-1a 在体外对 NAB 的抗原性是否低于 rIFNβ。使用两种体外测定法来定量分析 INSIGHT 研究中纳入的 115 份 MS 患者血清中的 NAB:细胞病变效应(CPE)测定法和 MxA 蛋白诱导测定法。通过比较固定剂量的 rIFNβ-1a Avonex®和 pegIFNβ-1a Plegridy®与血清稀释度,评估 NAB 交叉反应性。结果显示,在两种测定法中均观察到 NAB 交叉反应。y 截距(c)、一致线的斜率(b)、皮尔逊系数以及 Bland-Altman 分析表明,两种 IFNβ-1a 制剂的 NAB 滴度之间具有良好的一致性,CPE(c=0.1044±0.1305;b=0.8438±0.06654;r=0.587;偏差指数±SD=-0.01702±0.6334)和 MxA 蛋白诱导(c=0.08246±0.1229;b=0.8878±0.06613;r=0.615;偏差指数±SD=-0.09965±0.6467)测定法。在进一步的体内证据建立之前,临床医生在与 MS 患者讨论新的治疗选择时,应考虑当前表明 pegIFNβ-1a 和 rIFNβ 之间存在 NAB 交叉反应性的体外数据。