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多瘤病毒 JC 靶向 T 细胞疗法治疗造血细胞移植受者进行性多发性脑白质病。

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

机构信息

Clinica Pediatrica Università degli Studi di Milano Bicocca, Ospedale San Gerardo, Monza, Italy.

出版信息

Bone Marrow Transplant. 2011 Jul;46(7):987-92. doi: 10.1038/bmt.2010.221. Epub 2010 Oct 4.

Abstract

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.

摘要

与多瘤病毒 JC(JCV)感染相关的进行性多灶性白质脑病(PML)在异基因造血干细胞移植(HSCT)受者中通常是致命的。我们报告了一例 19 岁的 HSCT 患者,在严重移植物抗宿主病的长期免疫抑制后被诊断为 JCV 相关的 PML。抗病毒治疗和停止免疫抑制治疗后,未见短期神经改善。在用来自 VP1 和大 T 病毒蛋白的 15 肽刺激后,在体外产生了供体来源的 JCV Ag 特异性 CTL。在过继性 CTL 输注后,在外周血中显示出病毒特异性细胞毒性细胞,脑脊液中的 JCV-DNA 被清除,患者表现出明显改善。JCV 特异性 CTL 的过继性 T 淋巴细胞治疗是可行的,且无副作用。该病例提示,针对 JCV 的过继性 T 细胞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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