Willison Hugh J
Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, Glasgow Biomedical Research Centre, University of Glasgow, Glasgow, UK.
Methods Mol Biol. 2018;1804:173-188. doi: 10.1007/978-1-4939-8552-4_7.
Anti-ganglioside antibodies are principally associated with autoimmune peripheral neuropathies. In these disorders, immune attack is inadvertently directed at peripheral nerve by autoantibodies that target glycan structures borne by glycolipids, particularly gangliosides concentrated in nerve myelin and axons. The most thoroughly studied disorder is the acute paralytic disease, Guillain-Barré syndrome (GBS) in which IgG autoantibodies against gangliosides arise following acute infections, notably Campylobacter jejuni enteritis. Additionally, chronic autoimmune neuropathies are associated with IgM antibodies directed against many glycolipids including gangliosides. This introductory chapter briefly summarizes the immunological and pathological features of these disorders, focusing on the methodological development of antibody measurement and of animal models.
抗神经节苷脂抗体主要与自身免疫性周围神经病相关。在这些疾病中,自身抗体错误地将免疫攻击导向周围神经,这些自身抗体靶向糖脂所携带的聚糖结构,尤其是集中在神经髓鞘和轴突中的神经节苷脂。研究最深入的疾病是急性麻痹性疾病格林-巴利综合征(GBS),在该疾病中,针对神经节苷脂的IgG自身抗体在急性感染后出现,尤其是空肠弯曲菌肠炎。此外,慢性自身免疫性神经病与针对包括神经节苷脂在内的多种糖脂的IgM抗体有关。本章引言简要总结了这些疾病的免疫学和病理学特征,重点介绍了抗体检测方法和动物模型的发展。