Referral Center for Autonomic Nervous System Disorders, Department of Neurology, University Hospital Center Zagreb.
Clin Neuropharmacol. 2022;45(5):139-141. doi: 10.1097/WNF.0000000000000522. Epub 2022 Sep 7.
Alemtuzumab is a humanized anti-CD52 antibody that is registered for treatment of highly active relapsing-remitting multiple sclerosis. Disease activity after alemtuzumab treatment is infrequent. It may be a result of lack of lymphocyte depletion due to development of neutralizing autoantibodies. On the other hand, severe disease activity has been described after alemtuzumab, which is suggested to be caused by B-cell hyperpopulation. We present a case of a person with multiple sclerosis with severe disease activation after alemtuzumab administration that may represent paradoxical B cell-mediated disease activity. The patient was successfully treated with ocrelizumab.
阿仑单抗是一种人源化抗 CD52 抗体,已注册用于治疗高度活跃的复发缓解型多发性硬化症。阿仑单抗治疗后的疾病活动并不常见。这可能是由于产生中和自身抗体导致淋巴细胞耗竭不足所致。另一方面,阿仑单抗治疗后也有严重的疾病活动被描述,这被认为是由于 B 细胞过度增殖所致。我们报告了一例多发性硬化症患者,在接受阿仑单抗治疗后出现严重的疾病激活,这可能代表着矛盾的 B 细胞介导的疾病活动。该患者成功地接受了奥瑞珠单抗治疗。