Torres-Vega Estefanía, Mancheño Nuria, Cebrián-Silla Arantxa, Herranz-Pérez Vicente, Chumillas María J, Moris Germán, Joubert Bastien, Honnorat Jérôme, Sevilla Teresa, Vílchez Juan J, Dalmau Josep, Graus Francesc, García-Verdugo José Manuel, Bataller Luis
From the Laboratorio de Neurología (E.T.-V., T.S., J.J.V., L.B.), Instituto de Investigación Sanitaria La Fe, Hospital Universitario y Politécnico La Fe, CIBERER, Valencia; Servicio de Anatomía Patológica (N.M.), Servicio de Neurofisiología Clínica (M.J.C.), and Servicio de Neurología (T.S., J.J.V., L.B.), Hospital Universitario y Politécnico La Fe, Valencia; Laboratorio de Neurobiología Comparada (A.C.-S., V.H.-P., J.M.G.-V.), Instituto Cavanilles, Universidad de Valencia, CIBERNED; Servicio de Neurología (G.M.), Hospital Central de Asturias, Oviedo, Spain; French Reference Center on Paraneoplastic Neurological Syndrome (B.J., J.H.), Hospices Civils de Lyon, Hôpital Neurologique, Bron, and Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon-Université Claude Bernard Lyon 1, France; Laboratori de Neurologia (J.D., F.G.), Institut d´Investigacions Biomèdiques August Pi I Sunyer, CIBERER, Barcelona, Spain; and Department of Neurology (J.D.), University of Pennsylvania, Philadelphia, and Institució Catalana de Recerca i Estudis Avançats, Barcelona, Spain.
Neurology. 2017 Mar 28;88(13):1235-1242. doi: 10.1212/WNL.0000000000003778. Epub 2017 Mar 1.
To identify cell-surface antibodies in patients with neuromyotonia and to describe the main clinical implications.
Sera of 3 patients with thymoma-associated neuromyotonia and myasthenia gravis were used to immunoprecipitate and characterize neuronal cell-surface antigens using reported techniques. The clinical significance of antibodies against precipitated proteins was assessed with sera of 98 patients (neuromyotonia 46, myasthenia gravis 52, thymoma 42; 33 of them with overlapping syndromes) and 219 controls (other neurologic diseases, cancer, and healthy volunteers).
Immunoprecipitation studies identified 3 targets, including the Netrin-1 receptors DCC (deleted in colorectal carcinoma) and UNC5A (uncoordinated-5A) as well as Caspr2 (contactin-associated protein-like 2). Cell-based assays with these antigens showed that among the indicated patients, 9 had antibodies against Netrin-1 receptors (7 with additional Caspr2 antibodies) and 5 had isolated Caspr2 antibodies. Only one of the 219 controls had isolated Caspr2 antibodies with relapsing myelitis episodes. Among patients with neuromyotonia and/or myasthenia gravis, the presence of Netrin-1 receptor or Caspr2 antibodies predicted thymoma ( < 0.05). Coexisting Caspr2 and Netrin-1 receptor antibodies were associated with concurrent thymoma, myasthenia gravis, and neuromyotonia, often with Morvan syndrome ( = 0.009). Expression of DCC, UNC5A, and Caspr2 proteins was demonstrated in paraffin-embedded thymoma samples (3) and normal thymus.
Antibodies against Netrin-1 receptors (DCC and UNC5a) and Caspr2 often coexist and associate with thymoma in patients with neuromyotonia and myasthenia gravis.
This study provides Class III evidence that antibodies against Netrin-1 receptors can identify patients with thymoma (sensitivity 21.4%, specificity 100%).
鉴定神经性肌强直患者的细胞表面抗体,并描述其主要临床意义。
使用报道的技术,采用3例胸腺瘤相关神经性肌强直和重症肌无力患者的血清对神经元细胞表面抗原进行免疫沉淀和特性鉴定。用98例患者(神经性肌强直46例、重症肌无力52例、胸腺瘤42例;其中33例患有重叠综合征)和219例对照(其他神经系统疾病、癌症患者及健康志愿者)的血清评估针对沉淀蛋白的抗体的临床意义。
免疫沉淀研究鉴定出3个靶点,包括Netrin-1受体DCC(结直肠癌缺失基因)和UNC5A(不协调-5A)以及Caspr2(接触蛋白相关蛋白样2)。对这些抗原进行的细胞试验表明,在上述患者中,9例有针对Netrin-1受体的抗体(7例还伴有Caspr2抗体),5例有孤立的Caspr2抗体。219例对照中只有1例有孤立的Caspr2抗体并伴有复发性脊髓炎发作。在神经性肌强直和/或重症肌无力患者中,Netrin-1受体或Caspr2抗体的存在提示胸腺瘤(P<0.05)。共存的Caspr2和Netrin-1受体抗体与同时存在的胸腺瘤、重症肌无力和神经性肌强直相关,常伴有莫旺综合征(P=0.009)。在石蜡包埋的胸腺瘤样本(3例)和正常胸腺中证实了DCC、UNC5A和Caspr2蛋白的表达。
针对Netrin-1受体(DCC和UNC5a)和Caspr2的抗体在神经性肌强直和重症肌无力患者中常共存并与胸腺瘤相关。
本研究提供了III级证据,表明针对Netrin-1受体的抗体可鉴定胸腺瘤患者(敏感性21.4%,特异性100%)。