Hosoya Mitsuaki
Department of Pediatrics, Fukushima Medical University.
Rinsho Shinkeigaku. 2011 Nov;51(11):1047-50. doi: 10.5692/clinicalneurol.51.1047.
Subacute sclerosing panencephalitis (SSPE) is a progressive and fatal central nervous system disorder that results from a persistent SSPE virus infection. The efficacy of inosine pranobex, an antiviral/immunomodulator agent, remains controversial. Intraventricular interferon-alpha combined with oral inosine pranobex slows the progressive course of SSPE, but does not cure the disease. We examined a wide variety of antiviral compounds for their inhibitory effects on SSPE virus strains in vitro and in vivo, and found that ribavirin had potent inhibitory activity against SSPE. We tried to treat SSPE patients first with high-dose intravenous ribavirin therapy, and then with intraventricular ribavirin therapy. Ribavirin therapy seemed to have a certain effect on clinical courses of patients with SSPE. To reach the conclusion that ribavirin therapy is clinically effective, clinical trials on many cases will be required.
亚急性硬化性全脑炎(SSPE)是一种由持续性SSPE病毒感染导致的进行性致命性中枢神经系统疾病。抗病毒/免疫调节剂肌苷 pranobex 的疗效仍存在争议。脑室内注射α干扰素联合口服肌苷 pranobex 可减缓 SSPE 的进展过程,但无法治愈该疾病。我们在体外和体内研究了多种抗病毒化合物对 SSPE 病毒株的抑制作用,发现利巴韦林对 SSPE 具有强大的抑制活性。我们尝试先用大剂量静脉注射利巴韦林疗法治疗 SSPE 患者,然后采用脑室内注射利巴韦林疗法。利巴韦林疗法似乎对 SSPE 患者的临床病程有一定效果。要得出利巴韦林疗法在临床上有效的结论,还需要对许多病例进行临床试验。