Marcus D M
Department of Medicine, Baylor College of Medicine, Houston, TX 77030.
Ann Neurol. 1990;27 Suppl:S53-5. doi: 10.1002/ana.410270714.
Measurement of antibodies against gangliosides and other glycosphingolipids (GSLs) is technically demanding because of their low affinity for antigen. A recent workshop, in which twelve laboratories received a coded panel of sera containing anti-GM1 antibodies, demonstrated that the immunoassays varied widely in sensitivity and in criteria employed for a positive test. The fine specificity of anti-GSL antibodies should be characterized by analyzing their reactivity with a panel of GSLs with related structures. High-titer monoclonal IgM antibodies against gangliosides and sulfated carbohydrates appear to cause neuropathy in some patients. Low-titer polyclonal antibodies against gangliosides occur frequently in a variety of diseases, including autoimmune diseases without neurological symptoms. It is unclear whether these polyclonal antibodies are a primary manifestation or a consequence of the disease, and their clinical importance is uncertain at present.
由于抗神经节苷脂和其他糖鞘脂(GSLs)的抗体与抗原的亲和力较低,因此其检测在技术上要求较高。最近举办了一次研讨会,十二个实验室收到了一组含有抗GM1抗体的编码血清样本,结果表明免疫测定在灵敏度和阳性检测标准方面差异很大。抗GSL抗体的精细特异性应以分析其与一组结构相关的GSLs的反应性来表征。高滴度的抗神经节苷脂和硫酸化碳水化合物的单克隆IgM抗体似乎在一些患者中导致神经病变。低滴度的抗神经节苷脂多克隆抗体在包括无神经症状的自身免疫性疾病在内的多种疾病中经常出现。目前尚不清楚这些多克隆抗体是疾病的主要表现还是疾病的后果,其临床重要性也尚不确定。