Department of Neurology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ, United States.
Minnesota Department of Health, St. Paul, MN, United States.
J Neurol Sci. 2018 Feb 15;385:34-38. doi: 10.1016/j.jns.2017.12.005. Epub 2017 Dec 6.
Workers exposed to aerosolized brain in a swine-processing plant developed immune-mediated polyradiculoneuropathy (IP) possibly triggered by an immune response.
Immunohistochemistry results were correlated with electrophysiological variables to examine the immunopathogenesis of this disorder.
DESIGN/SETTING: Laboratory studies used normal nerve tissue that was exposed to sera from 12 IP patients; 10 exposed controls; and 10 unexposed controls. Clinical and electrophysiological data from IP patients were obtained from medical record reviews.
Analysis included electromyography results of IP patients and nerve conduction studies examining CMAP amplitude, distal motor latency, motor conduction velocity, F-wave latency, sensory nerve action potential amplitude, and sensory nerve conduction velocity. Case and control results were compared relative to distance from exposure.
Electrodiagnostic findings revealed prolongation of the distal and f-wave latencies suggestive of demyelination at the level of the nerve root and distal nerve terminals. Immunohistochemical results identified an antibody to the peripheral nerve, with staining at the level of the axolemma. Thus, IP may be a primary axonopathy with secondary paranodal demyelination causing the conduction changes. Staining of the distal and proximal portions of the nerve appears consistent with easier access through the blood-nerve barrier.
IP is an immune-mediated neuropathy related to antibodies to an axon-based antigen on peripheral nerves. Secondary paranodal demyelination is likely. Further studies to identify the primary axonal antigenic target would be useful.
在一家猪肉加工厂中,接触到雾化脑的工人可能会因免疫反应而患上免疫介导性多发性神经根神经病(IP)。
免疫组织化学结果与电生理学变量相关联,以检查这种疾病的免疫发病机制。
设计/设置:实验室研究使用正常神经组织,该组织暴露于 12 名 IP 患者的血清中;暴露对照 10 名;和 10 名未暴露对照组。从病历回顾中获得了 IP 患者的临床和电生理数据。
分析包括 IP 患者的肌电图结果和神经传导研究,检查 CMAP 幅度、远端运动潜伏期、运动传导速度、F 波潜伏期、感觉神经动作电位幅度和感觉神经传导速度。将病例和对照组的结果与暴露距离进行比较。
电诊断结果显示,远端和 F 波潜伏期延长,提示神经根和远端神经末梢脱髓鞘。免疫组织化学结果鉴定出一种针对周围神经的抗体,在轴突膜水平染色。因此,IP 可能是一种原发性轴索病,伴随后极脱髓鞘导致传导改变。神经的远端和近端部分的染色与通过血神经屏障的更容易进入相一致。
IP 是一种与周围神经上基于轴突的抗原抗体相关的免疫介导性神经病。继发性神经末梢脱髓鞘很可能。进一步研究以确定主要的轴突抗原靶标将是有用的。