Progressive Multifocal Leukoencephalopathy in Chimeric Antigen Receptor T-Cell Therapy Recipients: A Case Study.

Michelly Abreu, Chirag B Patel, Krina Patel, Fareed Khawaja, Sudhakar Tummala
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Abstract

Chimeric antigen receptor (CAR) T-cell therapy is a novel immunotherapy modality that has shown remarkable response rates in refractory hematologic malignancies, including multiple myeloma (MM). Cytokine release syndrome (CRS) and neurotoxicity are well-described side effects of this therapy. CAR T-cell therapy recipients are also at increased risk for infections due to immune dysfunction, history of multiple lines of therapy, history of lymphodepleting chemotherapy prior to cell infusion, and prolonged B-cell aplasia. Progressive multifocal leukoencephalopathy (PML) is an opportunistic disease of the central nervous system caused by the reactivation of JC virus (JCV) in the setting of immunosuppression, which leads to increased morbidity and mortality. Here, we present a patient treated with ciltacabtagene autoleucel for refractory MM who presented with PML around 2 months after receiving CAR T-cell therapy. This case emphasizes the risks for the development of PML in immunocompromised patients potentially related to persistent B-cell aplasia, hypogammaglobulinemia, and prolonged immunosuppression and discusses treatment approaches. Treatments for PML are mostly focused on reconstituting immunity. However, no adequate treatment strategy for PML has yet been established and further research is needed.

嵌合抗原受体t细胞治疗受者的进行性多灶性脑白质病:一个病例研究。
嵌合抗原受体(CAR) t细胞治疗是一种新的免疫治疗方式,在包括多发性骨髓瘤(MM)在内的难治性血液系统恶性肿瘤中显示出显着的应答率。细胞因子释放综合征(CRS)和神经毒性是这种治疗的良好副作用。由于免疫功能障碍、多种治疗史、细胞输注前的淋巴细胞消耗化疗史以及长期的b细胞发育不全,CAR - t细胞治疗接受者感染的风险也增加。进行性多灶性脑白质病(PML)是一种中枢神经系统的机会性疾病,在免疫抑制的情况下,由JC病毒(JCV)的再激活引起,导致发病率和死亡率增加。在这里,我们报告了一位接受CAR - t细胞治疗约2个月后出现PML的难治性MM患者。本病例强调了免疫功能低下患者发生PML的风险,可能与持续性b细胞发育不全、低γ球蛋白血症和长期免疫抑制有关,并讨论了治疗方法。PML的治疗主要集中在重建免疫。然而,目前还没有适当的PML治疗策略,需要进一步的研究。
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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