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高滴度IgG抗GM1抗体的临床关联

The clinical correlates of high-titer IgG anti-GM1 antibodies.

作者信息

Kornberg A J, Pestronk A, Bieser K, Ho T W, McKhann G M, Wu H S, Jiang Z

机构信息

Department of Neurology, Washington University School of Medicine, St. Louis, MO.

出版信息

Ann Neurol. 1994 Feb;35(2):234-7. doi: 10.1002/ana.410350217.

Abstract

Serum IgG anti-GM1 antibodies have been reported to occur in a variety of disorders, including Guillain-Barré syndrome and chronic polyneuropathies. Of over 5,000 serums tested in our laboratory, high titers of selective IgG anti-GM1 antibodies (> 1:1,000) and without binding to sulfatide were found in 35 patients. Clinical correlation revealed that almost all patients had axonal, motor neuropathies. One subgroup was comprised of individuals with an acute motor neuropathy, described either as an acute axonal Guillain-Barré-like syndrome that was occasionally associated with a prodrome of Campylobacter jejuni enteritis or as Chinese paralysis syndrome. A second group of patients had chronic asymmetric lower motor neuron (LMN) syndromes with no conduction block or other evidence of demyelination. The presence of selective high-titer IgG anti-GM1 antibody reactivity in serum is uncommon but when present is strongly associated with acute axonal motor neuropathies or chronic asymmetric LMN syndromes.

摘要

血清IgG抗GM1抗体已被报道出现在多种疾病中,包括格林-巴利综合征和慢性多发性神经病。在我们实验室检测的5000多份血清中,35例患者发现了高滴度的选择性IgG抗GM1抗体(>1:1000)且不与硫脂结合。临床相关性研究表明,几乎所有患者都患有轴索性运动神经病。一个亚组由患有急性运动神经病的个体组成,这些个体被描述为急性轴索性格林-巴利样综合征,偶尔与空肠弯曲菌肠炎前驱症状相关,或被描述为中国麻痹综合征。第二组患者患有慢性不对称性下运动神经元(LMN)综合征,无传导阻滞或其他脱髓鞘证据。血清中存在选择性高滴度IgG抗GM1抗体反应并不常见,但一旦出现,则与急性轴索性运动神经病或慢性不对称性LMN综合征密切相关。

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