An Unexpected Post-ocrelizumab Improvement in Glycaemic Control in a Patient with Multiple Sclerosis

O. Duz, Şebnem Bektaş, Abdullah Emre Askin, Erkingül Birday
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Abstract

Ocrelizumab, a novel member of disease-modifying therapies for multiple sclerosis (MS), is a humanised monoclonal antibody against the CD20 molecule on the surface of B cells. Reports on possible effects of this molecule in MS therapy have attracted a lot attention since its approval in 2017. The authors present a 31-year-old female patient who was diagnosed with MS in 2008, with a concomitant disease of Type 1 diabetes (T1D). The patient’s MS treatment included interferon-β1a and fingolimod prior to ocrelizumab initiation in 2019. In regard to the patient’s T1D course, they had poor glycaemic control despite regular follow-ups and strict treatment plans. Subsequent to the commencement of ocrelizumab therapy, a significant improvement was observed in their glycaemic control. The authors’ case study aims to raise motivation for further investigation and studies to evaluate this unexpected potential impact of ocrelizumab on T1D control.
ocrelizumab后对多发性硬化患者血糖控制的意外改善
Ocrelizumab是一种针对B细胞表面CD20分子的人源化单克隆抗体,是多发性硬化症(MS)疾病修饰疗法的新成员。自2017年获批以来,有关该分子在多发性硬化症治疗中可能作用的报道引起了广泛关注。作者报告了一位31岁的女性患者,她于2008年被诊断为多发性硬化症,并伴有1型糖尿病(T1D)。患者的MS治疗包括干扰素-β1a和芬戈莫,在2019年奥克雷单抗开始之前。对于患者的T1D病程,尽管有定期随访和严格的治疗计划,但他们的血糖控制很差。在开始ocrelizumab治疗后,观察到他们的血糖控制有显著改善。作者的案例研究旨在为进一步的调查和研究提供动力,以评估ocrelizumab对T1D控制的意想不到的潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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