Immunology Department, Centre Diagnóstic Biomédic, Hospital Clínic, Barcelona, Spain.
Neuroimmunology Program, Institut d'Investigacions Biomédiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Front Immunol. 2019 Apr 12;10:769. doi: 10.3389/fimmu.2019.00769. eCollection 2019.
SOX1 autoantibodies are considered markers of small cell lung cancer (SCLC) and paraneoplastic neurological syndromes (PNS) and are usually determined by commercial line blot in many clinical services. Recent studies suggested that SOX1 autoantibodies also occur in patients with neuropathies unrelated to SCLC, questioning the value of SOX1 autoantibodies as paraneoplastic biomarkers. Here, we compared the specificity and sensitivity of a commercial line blot (Euroimmun, Lübeck, Germany) with those of an in house cell-based assay (CBA) with HEK293 cells transfected with SOX1. Overall, 210 patients were included in the study, 139 patients with polyneuropathies without SCLC, and 71 with disorders associated with SOX1 autoantibodies detected with the in-house CBA. Forty one of these 71 cases had been referred to our laboratory for onconeuronal antibody assessment and 30/71 were patients with known PNS and SCLC. None of the patients with polyneuropathies had SOX1 autoantibodies by either line blot or CBA (specificity of the immunoblot: 100%; 95%C.I.: 97.8-100). Among the 71 patients with CBA SOX1 autoantibodies, only 53 were positive by line blot (sensitivity: 74.6%; 95%C.I.: 62.9-84.2). Lung cancer was detected in 37/41 (90%; 34 with SCLC) patients referred for onconeuronal antibody assessment and 34 of them also had a PNS. Our study confirms the association of SOX1 autoantibodies with SCLC and PNS. The line blot test misses 25% of the cases; therefore, to minimize the frequency of false negative results we recommend the use of a confirmatory test, such as CBA, in patients suspected to have a SCLC-related PNS.
SOX1 自身抗体被认为是小细胞肺癌 (SCLC) 和副肿瘤神经系统综合征 (PNS) 的标志物,通常在许多临床服务中通过商业线印迹来确定。最近的研究表明,SOX1 自身抗体也出现在与 SCLC 无关的神经病变患者中,这对 SOX1 自身抗体作为副肿瘤生物标志物的价值提出了质疑。在这里,我们比较了商业线印迹 (Euroimmun,吕贝克,德国) 与使用转染 SOX1 的 HEK293 细胞的内部基于细胞的测定 (CBA) 的特异性和敏感性。总的来说,研究纳入了 210 名患者,其中 139 名患有非 SCLC 的多发性神经病,71 名患有与内部 CBA 检测到的 SOX1 自身抗体相关的疾病。这些 71 例中有 41 例已转至我们的实验室进行神经元相关抗体评估,30/71 例为已知的 PNS 和 SCLC 患者。通过线印迹或 CBA,均未在患有多发性神经病的患者中检测到 SOX1 自身抗体(免疫印迹的特异性:100%;95%CI:97.8-100)。在 71 例 CBA SOX1 自身抗体阳性的患者中,只有 53 例线印迹阳性(敏感性:74.6%;95%CI:62.9-84.2)。在因神经元相关抗体评估而转至我们实验室的 41 例患者中,有 37 例 (90%;34 例为 SCLC) 检测到肺癌,其中 34 例也有 PNS。我们的研究证实了 SOX1 自身抗体与 SCLC 和 PNS 的关联。线印迹试验漏诊了 25%的病例;因此,为了尽量减少假阴性结果的频率,我们建议在怀疑患有与 SCLC 相关的 PNS 的患者中使用确认性试验,如 CBA。