Livrea P, Zimatore G B, Simone I L, Trojano M, Lepore V, Ferrara V, Lupo F A, Pedone D
J Neurol. 1980;223(1):1-12. doi: 10.1007/BF00313135.
Isoelectric focusing and quantitative estimation of serum and CSF IgG were performed in 85 patients with idiopathic polyneuropathy (IP), subdivided according to the clinical course (acute, subacute, recurrent, chronic). Acute IP very frequently had an increase of oligoclonal and/or polyclonal serum IgG during the progressive phase and blood-CSF barrier damage accompanied by polyclonal IgG intrathecal synthesis during the stationary phase. Polyclonal IgG intrathecal synthesis was also present in several not acute IP and seemed to forecast unfavorable course. Oligoclonal IgG synthesis occurs very rarely within CSF but is a frequent finding in serum of patients with IP. Abnormalities of the IgG serum pattern are neither specific for any clinical course of IP nor of prognostic value. The possible significance of such findings is discussed.
对85例特发性多发性神经病(IP)患者进行了血清和脑脊液IgG的等电聚焦及定量评估,这些患者根据临床病程(急性、亚急性、复发性、慢性)进行了细分。急性IP在进展期常出现寡克隆和/或多克隆血清IgG增加,在静止期伴有血脑屏障损害及鞘内多克隆IgG合成。在一些非急性IP中也存在鞘内多克隆IgG合成,且似乎预示病程不佳。寡克隆IgG合成在脑脊液中很少发生,但在IP患者血清中很常见。IgG血清模式异常对IP的任何临床病程均无特异性,也无预后价值。文中讨论了这些发现的可能意义。