Academisch Ziekenhuis and Diabetes Research Center, Brussels Free University-VUB, Brussels, Belgium.
Blood. 2010 Feb 11;115(6):1145-55. doi: 10.1182/blood-2009-02-204875. Epub 2009 Dec 9.
Here we report a unique situation in which an early and synchronized Epstein-Barr virus (EBV) reactivation was induced by a 6-day course of treatment with a humanized CD3-specific monoclonal antibody in patients with recent onset of type 1 diabetes. The virologic and immunologic analysis demonstrated that this reactivation was transient, self-limited, and isolated, associated with the rapid advent of an EBV-specific T-cell response. The anti-CD3 antibody administration induced short-lasting immunosuppression and minor yet clear-cut signs of T-cell activation that preceded viral reactivation. Early posttransplant monitoring of renal and islet allograft recipients showed that no comparable phenomenon was observed after the administration of full-dose immunosuppressive therapy. This EBV reactivation remains of no apparent clinical concern over the long term and should not preclude further development of therapeutic anti-CD3 antibodies. This phenomenon may also direct new research avenues to understand the still ill-defined nature of stimuli triggering EBV reactivation in vivo.
我们在此报告了一种独特的情况,即 6 天疗程的人源化抗 CD3 单克隆抗体治疗可诱导近期发生 1 型糖尿病患者的 EBV 早期和同步激活。病毒学和免疫学分析表明,这种再激活是短暂的、自限性的和孤立的,与 EBV 特异性 T 细胞反应的快速出现有关。抗 CD3 抗体给药诱导短暂的免疫抑制和轻微但明显的 T 细胞激活迹象,这些迹象先于病毒再激活。肾和胰岛移植物受者的移植后早期监测显示,在给予全剂量免疫抑制治疗后,未观察到类似的现象。这种 EBV 再激活在长期内没有明显的临床意义,不应排除进一步开发治疗性抗 CD3 抗体的可能性。这种现象也可能为理解体内触发 EBV 再激活的刺激因素的性质提供新的研究途径,目前这种性质仍不清楚。