Okuda Y, Sakoda S, Fujimura H, Nagata S, Yanagihara T, Bernard C C
Neuroimmunology Laboratory, La Trobe University, Bundoora, Victoria, 3083, Australia.
Biochem Biophys Res Commun. 2000 Aug 18;275(1):164-8. doi: 10.1006/bbrc.2000.3279.
A therapy aimed at blocking the Fas/Fas ligand (FasL) system was investigated using a relapsing form of experimental autoimmune encephalomyelitis (EAE) in mice, an animal model of multiple sclerosis (MS). Intracisternal administration of neutralizing antibody against FasL during the progression phase of EAE significantly reduced the severity of the disease with milder inflammation and myelin breakdown in the central nervous system (CNS). These results raised the possibility that the Fas/FasL system might contribute to tissue destruction in the CNS in the acute phase of EAE and that the intrathecal administration of neutralizing antibody against FasL may be beneficial for suppression of the acute phase of MS.
利用小鼠复发性实验性自身免疫性脑脊髓炎(EAE)(一种多发性硬化症(MS)的动物模型),对一种旨在阻断Fas/Fas配体(FasL)系统的疗法进行了研究。在EAE进展期经脑池内注射抗FasL中和抗体,可显著降低疾病严重程度,中枢神经系统(CNS)的炎症和髓鞘破坏减轻。这些结果提示,Fas/FasL系统可能在EAE急性期导致CNS组织破坏,鞘内注射抗FasL中和抗体可能有助于抑制MS急性期。