Steinman L, Conlon P
Department of Neurological Science, Stanford University, California 94305, USA.
J Clin Immunol. 2001 Mar;21(2):93-8. doi: 10.1023/a:1011020225433.
The development of antigen specific therapy for multiple sclerosis (MS) involves specifically suppressing undesired immune responses targeting the myelin sheath and underlying axon. We have recently reported some success with altered peptide ligands for a major target of the autoimmune response in MS. Antigen specific therapy has the potential to suppress undesirable autoimmunity, while leaving the rest of the immune system intact. Induction of an antigen specific Th1-to-Th2 shift could achieve this aim, once side effects, such as allergic responses, are minimized with optimal dosing.
多发性硬化症(MS)抗原特异性疗法的研发涉及特异性抑制针对髓鞘和潜在轴突的不良免疫反应。我们最近报道了针对MS自身免疫反应的一个主要靶点使用改变的肽配体取得了一些成功。抗原特异性疗法有潜力抑制不良自身免疫,同时使免疫系统的其余部分保持完整。一旦通过优化给药将诸如过敏反应等副作用降至最低,诱导抗原特异性的Th1向Th2转变就能实现这一目标。