Sánchez Gomar Ismael, Díaz Sánchez María, Uclés Sánchez Antonio José, Casado Chocán José Luis, Suárez-Luna Nela, Ramírez-Lorca Reposo, Villadiego Javier, Toledo-Aral Juan José, Echevarría Miriam
Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville 41013, Spain.
Unidad de Gestión Clínica de Neurociencias, Servicio de Neurología del Hospital Universitario Virgen del Rocío, Seville 41013, Spain.
Int J Mol Sci. 2016 Jul 23;17(8):1195. doi: 10.3390/ijms17081195.
Detection of IgG anti-Aquaporin-4 (AQP4) in serum of patients with Neuromyelitis optica syndrome disorders (NMOSD) has improved diagnosis of these processes and differentiation from Multiple sclerosis (MS). Recent findings also claim that a subgroup of patients with NMOSD, serum negative for IgG-anti-AQP4, present antibodies anti-AQP1 instead. Explore the presence of IgG-anti-AQP1 using a previously developed cell-based assay (CBA) highly sensitive to IgG-anti-AQP4. Serum of 205 patients diagnosed as NMOSD (8), multiple sclerosis (94), optic neuritis (39), idiopathic myelitis (29), other idiopathic demyelinating disorders of the central nervous system (9), other neurological diseases (18) and healthy controls (8), were used in a CBA over fixed HEK cells transfected with hAQP1-EGFP or hM23-AQP4-EGFP, treated with Triton X-100 and untreated. ELISA was also performed. Analysis of serum with our CBA indicated absence of anti-AQP1 antibodies, whereas in cells pretreated with detergent, noisy signal made reliable detection impossible. ELISA showed positive results in few serums. The low number of NMOSD serums included in our study reduces its power to conclude the specificity of AQP1 antibodies as new biomarkers of NMOSD. Our study does not sustain detection of anti-AQP1 in serum of NMOSD patients but further experiments are expected.
检测视神经脊髓炎谱系障碍(NMOSD)患者血清中的抗水通道蛋白4(AQP4)IgG,改善了这些疾病的诊断以及与多发性硬化症(MS)的鉴别诊断。最近的研究结果还表明,一部分IgG抗AQP4血清阴性的NMOSD患者存在抗AQP1抗体。使用先前开发的对IgG抗AQP4高度敏感的基于细胞的检测方法(CBA)探索抗AQP1 IgG的存在情况。将205例诊断为NMOSD(8例)、多发性硬化症(94例)、视神经炎(39例)、特发性脊髓炎(29例)、中枢神经系统其他特发性脱髓鞘疾病(9例)、其他神经系统疾病(18例)的患者血清以及健康对照者(8例)的血清,用于对转染了hAQP1-EGFP或hM23-AQP4-EGFP的固定HEK细胞进行CBA检测,细胞分别经过Triton X-100处理、未处理。同时也进行了ELISA检测。用我们的CBA分析血清表明不存在抗AQP1抗体,而在用去污剂预处理的细胞中,信号嘈杂使得可靠检测无法进行。ELISA在少数血清中显示出阳性结果。我们研究中纳入的NMOSD血清数量较少,降低了得出AQP1抗体作为NMOSD新生物标志物特异性结论的效力。我们的研究不支持在NMOSD患者血清中检测到抗AQP1,但期待进一步的实验。