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首页> 外文期刊>Developmental Immunology: Journal of Immunology Research >Evaluation of Clinical Interest of Anti-Aquaporin-4 Autoantibody Followup in Neuromyelitis Optica
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Evaluation of Clinical Interest of Anti-Aquaporin-4 Autoantibody Followup in Neuromyelitis Optica

机译:抗Aquaporin-4自身抗体随访在视神经脊髓炎中的临床意义评价

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摘要

Neuromyelitis optica (NMO) is an autoimmune disease in which a specific biomarker named NMO-IgG and directed against aquaporin-4 (AQP4) has been found. A correlation between disease activity and anti-AQP4 antibody (Ab) serum concentration or complement-mediated cytotoxicity has been reported, but the usefulness of longitudinal evaluation of these parameters remains to be evaluated in actual clinical practice. Thirty serum samples from 10 NMO patients positive for NMO-IgG were collected from 2006 to 2011. Anti-AQP4 Ab serum concentration and complement-mediated cytotoxicity were measured by flow cytometry using two quantitative cell-based assays (CBA) and compared with clinical parameters. We found a strong correlation between serum anti-AQP4 Ab concentration and complement-mediated cytotoxicity (P<0.0001). Nevertheless, neither relapse nor worsening of impairment level was closely associated with a significant increase in serum Ab concentration or cytotoxicity. These results suggest that complement-mediated serum cytotoxicity assessment does not provide extra insight compared to anti-AQP4 Ab serum concentration. Furthermore, none of these parameters appears closely related to disease activity and/or severity. Therefore, in clinical practice, serum anti-AQP4 reactivity seems not helpful as a predictive biomarker in the followup of NMO patients as a means of predicting the onset of a relapse and adapting the treatment accordingly.
机译:视神经脊髓炎(NMO)是一种自身免疫性疾病,其中已发现一种名为NMO-IgG且针对水通道蛋白4(AQP4)的特定生物标记。已经报道了疾病活性与抗AQP4抗体(Ab)血清浓度或补体介导的细胞毒性之间的相关性,但纵向评估这些参数的有用性仍有待在实际临床实践中进行评估。从2006年至2011年,从30例NMO-IgG阳性的10例NMO患者中收集了30份血清样品。使用两种基于细胞的定量分析(CBA),通过流式细胞仪测量了抗AQP4 Ab血清浓度和补体介导的细胞毒性。 。我们发现血清抗AQP4 Ab浓度与补体介导的细胞毒性之间有很强的相关性(P <0.0001)。然而,复发或损伤水平的恶化都与血清抗体浓度或细胞毒性的显着增加没有密切关系。这些结果表明,与抗AQP4 Ab血清浓度相比,补体介导的血清细胞毒性评估没有提供额外的见识。此外,这些参数均未显示与疾病活动和/或严重程度密切相关。因此,在临床实践中,血清抗AQP4反应性似乎无助于NMO患者随访中的预测生物标志物,作为预测复发发作和相应调整治疗的手段。

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