Chanson Jean-Baptiste, Alame Melissa, Collongues Nicolas, Blanc Frédéric, Fleury Marie, Rudolf Gabrielle, de Seze Jérôme, Vincent Thierry
Département de Neurologie, Hôpitaux Universitaires de Strasbourg, 1 Avenue Molière, 67091 Strasbourg, France.
Clin Dev Immunol. 2013;2013:146219. doi: 10.1155/2013/146219. Epub 2013 Apr 28.
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.
视神经脊髓炎(NMO)是一种自身免疫性疾病,在该疾病中发现了一种名为NMO-IgG且针对水通道蛋白4(AQP4)的特异性生物标志物。已有报道称疾病活动与抗AQP4抗体(Ab)血清浓度或补体介导的细胞毒性之间存在相关性,但在实际临床实践中,对这些参数进行纵向评估的实用性仍有待评估。2006年至2011年期间,收集了10例NMO-IgG阳性的NMO患者的30份血清样本。使用两种基于细胞的定量检测方法(CBA)通过流式细胞术测量抗AQP4 Ab血清浓度和补体介导的细胞毒性,并与临床参数进行比较。我们发现血清抗AQP4 Ab浓度与补体介导的细胞毒性之间存在强相关性(P < 0.0001)。然而,复发或损伤水平的恶化均与血清Ab浓度或细胞毒性的显著增加没有密切关联。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并不能提供额外的见解。此外,这些参数似乎均与疾病活动和/或严重程度没有密切关系。因此,在临床实践中,血清抗AQP4反应性作为预测生物标志物在NMO患者随访中预测复发发作并据此调整治疗方面似乎并无帮助。