O'Brien Kate, Gran Bruno, Rostami Abdolmohamad
Division of Clinical Neurology, University of Nottingham, UK.
Immunotherapy. 2010 Jan;2(1):99-115. doi: 10.2217/imt.09.61.
One of the reasons multiple sclerosis (MS) has been considered a T-cell mediated autoimmune disease is that a similar experimental disease can be induced in certain rodents and primates by immunization with myelin antigens, leading to T-cell-mediated inflammatory demyelination in the CNS. In addition, most if not all pharmacological treatments available for MS are biologically active on T cells. In this article we review the principles of T-cell-based immunotherapies and the specific actions of current and novel treatments on T-cell functions, when these are known. For both licensed and innovative agents, we also discuss biological actions on other immune cell types. Finally, we offer a brief perspective on expected changes in the use of MS immunotherapies in the near future.
多发性硬化症(MS)被视为T细胞介导的自身免疫性疾病的原因之一是,通过用髓磷脂抗原免疫某些啮齿动物和灵长类动物,可诱发类似的实验性疾病,导致中枢神经系统中T细胞介导的炎性脱髓鞘。此外,MS可用的大多数(如果不是全部)药物治疗对T细胞具有生物活性。在本文中,我们回顾了基于T细胞的免疫疗法的原理,以及当前和新型治疗方法对T细胞功能的具体作用(已知的情况下)。对于已获许可的药物和创新药物,我们还讨论了它们对其他免疫细胞类型的生物学作用。最后,我们简要展望了MS免疫疗法在不久的将来使用方面的预期变化。