Pirko I, Kuntz N L, Patterson M, Keegan B M, Weinshenker B G, Rodriguez M
Department of Neurology, Mayo Clinic, Rochester, MN 55902, USA.
Neurology. 2003 May 27;60(10):1697-9. doi: 10.1212/01.wnl.0000064163.94122.eb.
Reported are three children with MS who responded dramatically to interferon-beta (IFNbeta) therapy. While on immunomodulatory therapy, they developed chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) that responded to IV immunoglobulin (IVIG) administration. These cases emphasize two interesting observations: 1) IFNbeta treatment did not prevent development of CIDP; 2) CIDP in the context of MS responded to IVIG, even though IVIG had no therapeutic effect on the central demyelinating disease.
报告了三名患有多发性硬化症(MS)的儿童,他们对β-干扰素(IFNβ)治疗反应显著。在接受免疫调节治疗期间,他们患上了慢性炎症性脱髓鞘性多发性神经根神经病(CIDP),对静脉注射免疫球蛋白(IVIG)治疗有反应。这些病例强调了两个有趣的观察结果:1)IFNβ治疗未能预防CIDP的发生;2)MS背景下的CIDP对IVIG有反应,尽管IVIG对中枢性脱髓鞘疾病没有治疗效果。