Institute of Immunology, Faculty of Medicine, University of Oslo, Oslo University Hospital, Rikshospitalet, 0027 Oslo, Norway.
Toxins (Basel). 2010 Apr;2(4):856-77. doi: 10.3390/toxins2040856. Epub 2010 Apr 22.
The relationship between immune responses to self-antigens and autoimmune disease is unclear. In contrast to its animal model experimental autoimmune encephalomyelitis (EAE), which is driven by T cell responses to myelin antigens, the target antigen of the intrathecal immune response in multiple sclerosis (MS) has not been identified. Although the immune response in MS contributes significantly to tissue destruction, the action of immunocompetent cells within the central nervous system (CNS) may also hold therapeutic potential. Thus, treatment of MS patients with glatiramer acetate triggers a protective immune response. Here we review the immunopathogenesis of MS and some recent findings on the mechanism of glatiramer acetate (GA).
自身抗原的免疫反应与自身免疫性疾病之间的关系尚不清楚。与动物模型实验性自身免疫性脑脊髓炎(EAE)不同,EAE 是由 T 细胞对髓鞘抗原的反应所驱动,多发性硬化症(MS)鞘内免疫反应的靶抗原尚未确定。虽然 MS 中的免疫反应对组织破坏有重要贡献,但中枢神经系统(CNS)内免疫活性细胞的作用也可能具有治疗潜力。因此,用醋酸格拉替雷治疗 MS 患者会引发保护性免疫反应。本文综述了 MS 的免疫发病机制和关于醋酸格拉替雷(GA)作用机制的一些新发现。