首页> 美国卫生研究院文献>NeuroRx >Ocrelizumab and Other CD20+ B-Cell-Depleting Therapies in Multiple Sclerosis
【2h】

Ocrelizumab and Other CD20+ B-Cell-Depleting Therapies in Multiple Sclerosis

机译:Ocrelizumab和其他CD20 + B细胞耗竭疗法在多发性硬化症中的作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Selective depletion of CD20+ B cells by anti-CD20 monoclonal antibodies as monotherapy in multiple sclerosis (MS) profoundly suppresses acute inflammatory disease activity and signifies an important advance in the treatment of relapsing-remitting MS. Ocrelizumab, a humanized anti-CD20 monoclonal antibody, is also the first proven therapy to lessen disability progression in primary progressive MS—a breakthrough for patients with a disease that had no proven therapy. Ocrelizumab is generally well tolerated, with the most common adverse events experienced being infusion reactions and infections. In ocrelizumab trials in MS a numerical imbalance in the risk of malignancies was observed. In this article, we review advances in anti-CD20 B-cell-depleting biological therapies for MS, including ocrelizumab, rituximab, and ofatumumab.Electronic supplementary materialThe online version of this article (doi:10.1007/s13311-017-0557-4) contains supplementary material, which is available to authorized users.
机译:在多发性硬化症(MS)中,抗CD20单克隆抗体作为单一疗法对CD20 + B细胞的选择性消耗,将极大地抑制急性炎症性疾病的活动,并标志着复发性MS的治疗方面的重要进展。 Ocrelizumab,一种人源化抗CD20单克隆抗体,也是减少原发性进行性MS的残疾进展的第一种行之有效的疗法,这对未经证实的疾病患者来说是一项突破。 Ocrelizumab通常耐受性良好,最常见的不良事件是输注反应和感染。在MS的ocrelizumab试验中,观察到恶性肿瘤风险的数值失衡。在本文中,我们回顾了抗CD20 B细胞耗尽的MS生物疗法的进展,包括ocrelizumab,rituximab和ofatumumab。电子补充材料本文的在线版本(doi:10.1007 / s13311-017-0557-4)包含补充材料,授权用户可以使用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号