多瘤病毒感染:述评

IF 5.3 3区 医学 Q1 INFECTIOUS DISEASES
Infectious Diseases and Therapy Pub Date : 2025-09-01 Epub Date: 2025-07-27 DOI:10.1007/s40121-025-01199-y
Meital Elbaz, Dafna Yahav, Yair Mina, Alaa Atamna
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引用次数: 0

摘要

进行性多灶性白质脑病(PML)是由约翰·坎宁安多瘤病毒(JCPyV)引起的一种毁灭性的、通常是致命的中枢神经系统感染。PML是在HIV、器官移植、严重炎症性疾病以及越来越多的癌症和自身免疫性疾病的现代治疗患者的细胞免疫受损的情况下,由JCPyV再激活引起的。临床和影像学表现符合诊断,加上脑脊液(CSF) PCR显示JCPyV,被认为是诊断。由于没有有效的抗病毒治疗方法,恢复免疫功能是PML治疗的关键组成部分。新的免疫治疗方法可以改善PML。免疫治疗干预,如使用检查点抑制剂和病毒特异性t细胞,已经显示出有希望的结果,但需要更多的数据。在这篇综述中,我们总结了JCPyV神经综合征的危险因素、临床、实验室和放射学特征,并提出了一种治疗算法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

JC Polyomavirus Infection: A Narrative Review.

JC Polyomavirus Infection: A Narrative Review.

Progressive multifocal leukoencephalopathy (PML) is a devastating and often fatal central nervous system infection caused by John Cunningham polyomavirus virus (JCPyV). PML results from JCPyV reactivation in the setting of impaired cellular immunity in patients with HIV, organ transplantation, severe inflammatory disease, and an increasing number of modern treatments for cancer and autoimmune diseases. The presence of clinical and imaging manifestations consistent with the diagnosis coupled with the demonstration of JCPyV by PCR in cerebrospinal fluid (CSF) are considered diagnostic. Since there are no effective antiviral treatments available, restoring immune function is a key component in PML treatment. Novel immunotherapeutic approaches can ameliorate PML. Immunotherapeutic interventions, such as use of checkpoint inhibitors and viral specific T-cell, have shown promising results, but additional data are needed. In this review, we summarize the available data on risk factors for JCPyV neurological syndrome, clinical, laboratory, and radiological features, and propose an algorithm for management.

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来源期刊
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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