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Polyomavirus JC-targeted T-cell therapy for progressive multiple leukoencephalopathy in a hematopoietic cell transplantation recipient

机译:多瘤病毒JC靶向T细胞疗法治疗造血细胞移植受者的进行性多发性白质脑病

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摘要

Progressive multifocal leukoencephalopathy (PML) associated with polyomavirus JC (JCV) infection has been reported to be usually fatal in allogeneic hematopoietic SCT (HSCT) recipients. We present the case of a 19-year-old HSCT patient diagnosed with JCV-associated PML after prolonged immunosuppression for severe GVHD. No short-term neurological improvement was observed after antiviral treatment and discontinuation of immunosuppressive therapy. Donor-derived JCV Ag-specific CTLs were generated in vitro after stimulation with 15-mer peptides derived from VP1 and large T viral proteins. After adoptive CTL infusion, virus-specific cytotoxic cells were shown in the peripheral blood, JCV-DNA was cleared in the cerebrospinal fluid and the patient showed remarkable improvement. Adoptive T-lymphocyte therapy with JCV-specific CTLs was feasible and had no side effects. This case suggests that adoptive transfer of JCV-targeted CTLs may contribute to restore JCV-specific immune competence and control PML in transplanted patients.
机译:据报道,与多瘤病毒JC(JCV)感染有关的进行性多灶性白质脑病(PML)通常在同种异体造血SCT(HSCT)受体中致命。我们提出了对严重GVHD进行长期免疫抑制后被诊断为JCV相关PML的19岁HSCT患者的病例。抗病毒治疗和免疫抑制治疗终止后未观察到短期神经系统改善。在用源自VP1的15-mer肽和大T病毒蛋白刺激后,体外产生了供体来源的JCV Ag特异性CTL。过继CTL输注后,外周血中显示出病毒特异性的细胞毒性细胞,脑脊液中的JCV-DNA被清除,患者表现出明显的改善。采用JCV特异的CTL进行过继性T淋巴细胞疗法是可行的,并且没有副作用。这种情况表明,针对JCV的CTL的过继转移可能有助于恢复JCV特异性免疫能力并控制移植患者的PML。

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