Vivekanandan Govinathan, Abubacker Ansha P, Myneni Revathi, Chawla Harsh V, Iqbal Aimen, Grewal Amit, Ndakotsu Andrew, Khan Safeera
Internal Medicine, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Emergency Medicine, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Cureus. 2021 Apr 30;13(4):e14764. doi: 10.7759/cureus.14764.
Natalizumab, a monoclonal antibody acting on alpha4 integrin receptors, is frequently used to treat multiple sclerosis patients. The biggest downside is the risk of development of progressive multifocal leukoencephalopathy, an immune-related condition affecting mainly the central nervous system. The presence of the John Cunningham virus (JCV) and its reactivation is an important factor in the development of progressive multifocal leukoencephalopathy (PML). This study highlights its different proposed mechanism and risk factors strongly related to natalizumab-induced progressive multifocal leukoencephalopathy. The pieces of literature will also be reviewed to look for a relation between the JCV and natalizumab-induced progressive multifocal leukoencephalopathy in multiple sclerosis treated patients. The articles were searched from three databases and reviewed systematically. The inclusion criteria for this study were patients aged 20-50 years, English language paper, full-text availability, and human studies, whereas articles on patients with AIDS and cancer-related disease prior to natalizumab treatment were excluded. Out of 6531 articles identified after applying the search strategy on three main databases PubMed, Google Scholar, and ResearchGate, a total of 32 articles were finalized for the review. This study follows the guidelines listed in the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) checklist 2009. The data collected from these finalized articles were pertaining to the risk factor related to natalizumab induced progressive multifocal leukoencephalopathy and the mechanism related to its pathogenesis. Natalizumab is known to have the potential to cause progressive multifocal leukoencephalopathy in treated patients; here, we evaluate a close relationship of its related risk factors. The articles studied exhibit a close relationship between the length of natalizumab treatment and the presence of the JCV before infusion of natalizumab. From our analysis, it seems that the mechanism related to natalizumab-induced PML is strongly related to antigen-specific T cells and its effects. The frequency of monitoring and vigilance on the management of patients treated with natalizumab will help detect progressive multifocal leukoencephalopathy.
那他珠单抗是一种作用于α4整合素受体的单克隆抗体,常用于治疗多发性硬化症患者。最大的缺点是有发生进行性多灶性白质脑病的风险,这是一种主要影响中枢神经系统的免疫相关疾病。约翰·坎宁安病毒(JCV)的存在及其再激活是进行性多灶性白质脑病(PML)发生的一个重要因素。本研究强调了其不同的推测机制以及与那他珠单抗诱导的进行性多灶性白质脑病密切相关的危险因素。还将回顾相关文献,以寻找JCV与接受那他珠单抗治疗的多发性硬化症患者中那他珠单抗诱导的进行性多灶性白质脑病之间的关系。从三个数据库检索文章并进行系统回顾。本研究的纳入标准为年龄在20至50岁之间的患者、英文论文、全文可获取以及人体研究,而排除那他珠单抗治疗前患有艾滋病和癌症相关疾病患者的文章。在对三个主要数据库PubMed、谷歌学术和ResearchGate应用检索策略后识别出的6531篇文章中,共有32篇文章最终被纳入综述。本研究遵循2009年系统评价和Meta分析优先报告项目(PRISMA)清单中列出的指南。从这些最终文章中收集的数据与那他珠单抗诱导的进行性多灶性白质脑病相关的危险因素及其发病机制有关。已知那他珠单抗有可能在接受治疗的患者中引起进行性多灶性白质脑病;在此,我们评估其相关危险因素的密切关系。所研究的文章显示那他珠单抗治疗时长与输注那他珠单抗前JCV的存在之间存在密切关系。从我们的分析来看,那他珠单抗诱导PML的机制似乎与抗原特异性T细胞及其作用密切相关。对接受那他珠单抗治疗的患者进行管理时的监测频率和警惕性将有助于检测进行性多灶性白质脑病。