医学
进行性多灶性白质脑病
白质脑病
JC病毒
BK病毒
病毒学
肾移植
肾
肾移植
病毒
免疫学
病理
内科学
疾病
作者
Abiu Sempere,Fritz Dieckmann,Francesc Rudilla,Fritz Dieckmann,Fritz Dieckmann,Cristina Prat‐Vidal,Margarita Codinach,Frederic Cofán,Vicens Torregrossa,Fritz Dieckmann,Marta Bodro
标识
DOI:10.1016/j.ajt.2024.05.003
摘要
The strategy for progressive multifocal leukoencephalopathy (PML) in solid organ transplant recipients primarily focuses on reducing immunosuppressive therapy. However, this approach offers limited efficacy and carries a high risk of graft loss. Here, we present the case of a 64-year-old male kidney transplant recipient with a high degree of immunosuppression who developed PML in October 2022. Despite the standard reduction of immunosuppressive therapy, the patient's condition continued to deteriorate, as evidenced by worsening neurological symptoms and increasing JC virus (JCV) DNA levels in cerebrospinal fluid. This prompted the innovative use of BKPyV-virus-specific T cell (BKPyV-VST) therapy, given the genetic similarities between BK and JCVs. Infusion of third-party donor BKPyV-VST resulted in clinical stabilization, a significant reduction in JCV-DNA levels, and the emergence of a JCV-specific T cell response, as observed in enzyme-linked immunospot assays and TCRβ sequencing. This represents the first case report of successful third-party BKPyV-VST therapy in a kidney recipient presenting PML, without graft-versus-host disease or graft dysfunction.
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