Sadowski Marcin, Wisniewski Thomas
Department of Neurology, New York University School of Medicine, 550 First Avenue, MHL Rm. HN 419, New York, NY 10016, USA.
Expert Rev Vaccines. 2004 Jun;3(3):279-90. doi: 10.1586/14760584.3.3.279.
Neurodegenerative disorders are becoming increasingly common and an ever greater healthcare burden, as the average age in Western populations rises. Many of these are conformational disorders, which are characterized by the accumulation of a host protein that undergoes a structural change increasing its beta-sheet content, rendering it toxic. The most common of these illnesses is Alzheimer's disease. Prion diseases are also conformational disorders, which are currently less common than Alzheimer's disease, however, these illnesses have no treatment and are universally rapidly fatal. The emergence of new variant Creutzfeldt-Jakob disease has raised the possibility of a large population at risk for this illness, as well as causing great concern regarding the safety of blood bank supplies. Recently, immune modulation has emerged as a highly promising therapeutic strategy for both Alzheimer's and prion diseases. We and others have demonstrated in both Alzheimer's and prion disease animal models that vaccination can dramatically improve the course of the illness. A human trial of an Alzheimer's disease vaccine using A beta1-42 was halted due to toxicity in a minority of patients (6%). However, recent data suggests that patients with a humoral response to A beta benefited cognitively from the vaccine. Toxicity in this human trial has been linked to excessive cell-mediated immunity. Novel vaccine strategies are under development for both Alzheimer's disease and prionoses which are predicted to have few or no significant side effects, while being efficacious.
随着西方人群平均年龄的上升,神经退行性疾病正变得越来越普遍,医疗负担也日益加重。其中许多是构象性疾病,其特征是一种宿主蛋白发生积累,该蛋白经历结构变化,增加其β-折叠含量,从而变得有毒。这些疾病中最常见的是阿尔茨海默病。朊病毒疾病也是构象性疾病,目前不如阿尔茨海默病常见,然而,这些疾病无法治疗,普遍会迅速致命。新型变异型克雅氏病的出现增加了大量人群面临这种疾病风险的可能性,同时也引发了对血库供应安全的极大担忧。最近,免疫调节已成为治疗阿尔茨海默病和朊病毒疾病极具前景的治疗策略。我们和其他人在阿尔茨海默病和朊病毒疾病动物模型中均已证明,接种疫苗可显著改善疾病进程。一项使用β-淀粉样蛋白1-42的阿尔茨海默病疫苗人体试验因少数患者(6%)出现毒性反应而停止。然而,最近的数据表明,对β-淀粉样蛋白产生体液反应的患者在认知方面从疫苗中获益。该人体试验中的毒性反应与过度的细胞介导免疫有关。目前正在为阿尔茨海默病和朊病毒病开发新的疫苗策略,预计这些策略几乎没有或没有显著副作用,同时具有疗效。