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Alemtuzumab for multiple sclerosis: the new concept of immunomodulation

机译:阿仑单抗治疗多发性硬化:免疫调节的新概念

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Alemtuzumab (Lemtrada?) is a humanized anti-CD52 IgG1 monoclonal antibody that depletes CD52-expressing cells from the circulation. Robust clinical and radiologic data, derived from clinical trials and long-term observational studies, indicate that alemtuzumab induces a marked immunosuppression related to the depletion of circulating T and B lymphocytes. However, recent advances suggest that the long-term clinical effects of alemtuzumab are probably due to unique qualitative changes in the process of lymphocyte repopulation of the immune system. This leads to a particular rebalancing of the immune system. In this paper we review the immunomodulatory mechanisms underlying the therapeutic effect of alemtuzumab in pre-clinical models and in patients with relapsing remitting multiple sclerosis (RRMS), and stress the importance of a monoclonal antibody-based immunosuppression for treating the severe forms of RRMS. Alemtuzumab has many features of the ideal immunomodulatory drug: rapid biological and clinical actions and and long-lasting benefit. Alemtuzumab can be used as rescue therapy or as first line drug in severe-onset MS. Thus, the availability of alemtuzumab constitutes a significant step forward in the therapy of MS.
机译:Alemtuzumab(Lemtrada?)是一种人源化的抗CD52 IgG1单克隆抗体,可从循环中消耗表达CD52的细胞。来自临床试验和长期观察研究的可靠的临床和放射学数据表明,阿仑单抗可引起与循环T和B淋巴细胞消耗相关的明显免疫抑制。但是,最近的进展表明,Alemtuzumab的长期临床效果可能是由于免疫系统淋巴细胞重新聚集过程中独特的质变所致。这导致免疫系统的特定重新平衡。在本文中,我们综述了Alemtuzumab在临床前模型和复发缓解型多发性硬化症(RRMS)患者中治疗作用的潜在免疫调节机制,并强调了基于单克隆抗体的免疫抑制对于治疗严重形式的RRMS的重要性。 Alemtuzumab具有理想免疫调节药物的许多功能:快速的生物学和临床作用以及持久的益处。 Alemtuzumab可用作抢救治疗或重症MS的一线药物。因此,alemtuzumab的可用性构成了MS治疗的重要一步。

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