Department of Clinical Neurosciences, University of Cambridge, Level 6, Block A, Box 165, Addenbrookes Hospital, Hills Road, Cambridge CB2 0QQ, UK.
Ther Adv Chronic Dis. 2013 May;4(3):97-103. doi: 10.1177/2040622313479137.
Alemtuzumab was first used in multiple sclerosis in 1991. It is a monoclonal antibody which is directed against CD52, a protein of unknown function on lymphocytes. Alemtuzumab causes a lymphopenia, following which homeostatic reconstitution leads to prolonged alteration of the immune repertoire. This reduces the risk of relapse and disability accumulation in multiple sclerosis; it is the only drug to show superiority over interferon β-1a in disability outcomes in a monotherapy phase III trial. It should be used with a parallel risk management programme to identify the principal adverse effects of alemtuzumab, especially secondary autoimmunity months or years later, mainly against the thyroid but also immune thrombocytopenia. This review charts the development of alemtuzumab as a drug for multiple sclerosis and summarizes the latest clinical trial data.
阿仑单抗于 1991 年首次用于多发性硬化症。它是一种针对 CD52 的单克隆抗体,CD52 是淋巴细胞上一种功能未知的蛋白质。阿仑单抗引起淋巴细胞减少症,随后的体内平衡重建导致免疫受体谱的长期改变。这降低了多发性硬化症复发和残疾累积的风险;它是唯一一种在单药治疗 III 期临床试验中在残疾结局方面优于干扰素β-1a 的药物。应使用平行的风险管理方案来识别阿仑单抗的主要不良反应,特别是数月或数年后的继发性自身免疫,主要针对甲状腺,但也包括免疫性血小板减少症。本综述描述了阿仑单抗作为多发性硬化症药物的发展,并总结了最新的临床试验数据。