Tüzün Erdem, Li Jing, Saini Shamsher S, Yang Huan, Christadoss Premkumar
Department of Neurology, University of Istanbul, Istanbul, Turkey.
Adv Exp Med Biol. 2008;632:265-72.
Mice deficient for classical complement pathway (CCP) factor C4 are resistant to antibody and complement mediated experimental autoimmune myasthenia gravis (EAMG). Anti-C1q antibody administration before or following acetylcholine receptor immunization suppresses EAMG development by reducing lymph node cell IL-6 production and neuromuscular junction IgG, C3 and C5b-C9 deposition. This effect is achieved by treating mice with 10 microg of anti-C1q antibody, twice weekly for 4 weeks. Treatment with a higher amount of anti-C1q antibody gives rise to increased serum anti-acetylcholine receptor antibody, immune complex and C3 levels, facilitates kidney C3 and IgG deposits and thus reduces the treatment efficacy. C4 KO and anti-C1q antibody treated mice display normal immune system functions and intact antibody production capacity. Furthermore, CCP inhibition preserves alternative complement pathway activation, which is required for host defense against microorganisms. Therefore, CCP inhibition might constitute a specific treatment approach for not only myasthenia gravis but also other complement mediated autoimmune diseases.
缺乏经典补体途径(CCP)因子C4的小鼠对抗体和补体介导的实验性自身免疫性重症肌无力(EAMG)具有抗性。在乙酰胆碱受体免疫之前或之后给予抗C1q抗体,可通过减少淋巴结细胞IL-6的产生以及神经肌肉接头处IgG、C3和C5b-C9的沉积来抑制EAMG的发展。通过用10微克抗C1q抗体治疗小鼠,每周两次,持续4周可实现这一效果。用更高剂量的抗C1q抗体治疗会导致血清抗乙酰胆碱受体抗体、免疫复合物和C3水平升高,促进肾脏C3和IgG沉积,从而降低治疗效果。C4基因敲除和抗C1q抗体治疗的小鼠表现出正常的免疫系统功能和完整的抗体产生能力。此外,抑制CCP可保留替代补体途径的激活,这是宿主抵御微生物所必需的。因此,抑制CCP不仅可能构成重症肌无力的一种特异性治疗方法,也可能用于其他补体介导的自身免疫性疾病。