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单纯疱疹病毒性脑炎的免疫调节策略。

Immunomodulatory Strategies in Herpes Simplex Virus Encephalitis.

机构信息

Research Center in Infectious Diseases, CHU de Quebec-Laval University, Quebec City, Canada.

Research Center in Infectious Diseases, CHU de Quebec-Laval University, Quebec City, Canada

出版信息

Clin Microbiol Rev. 2020 Feb 12;33(2). doi: 10.1128/CMR.00105-19. Print 2020 Mar 18.

Abstract

Herpes simplex virus 1 (HSV-1) can be responsible for life-threatening HSV encephalitis (HSE). The mortality rate of patients with HSE who do not receive antiviral treatment is 70%, with most survivors suffering from permanent neurological sequelae. The use of intravenous acyclovir together with improved diagnostic technologies such as PCR and magnetic resonance imaging has resulted in a reduction in the mortality rate to close to 20%. However, 70% of surviving patients still do not recover complete neurological functions. Thus, there is an urgent need to develop more effective treatments for a better clinical outcome. It is well recognized that cerebral damage resulting from HSE is caused by viral replication together with an overzealous inflammatory response. Both of these processes constitute potential targets for the development of innovative therapies against HSE. In this review, we discuss recent progress in therapy that may be used to ameliorate the outcome of patients with HSE, with a particular emphasis on immunomodulatory agents. Ideally, the administration of adjunctive immunomodulatory drugs should be initiated during the rise of the inflammatory response, and its duration should be limited in time to reduce undesired effects. This critical time frame should be optimized by the identification of reliable biomarkers of inflammation.

摘要

单纯疱疹病毒 1(HSV-1)可导致危及生命的单纯疱疹病毒性脑炎(HSE)。未接受抗病毒治疗的 HSE 患者的死亡率为 70%,大多数幸存者都患有永久性神经后遗症。阿昔洛韦静脉注射与聚合酶链反应(PCR)和磁共振成像等改进的诊断技术的结合使用,已将死亡率降低到接近 20%。然而,仍有 70%的存活患者没有完全恢复神经功能。因此,迫切需要开发更有效的治疗方法以获得更好的临床结果。众所周知,HSE 引起的脑损伤是由病毒复制和过度活跃的炎症反应共同引起的。这两个过程都是针对 HSE 开发创新疗法的潜在靶点。在这篇综述中,我们讨论了可能用于改善 HSE 患者预后的治疗方法的最新进展,特别强调了免疫调节剂。理想情况下,应在炎症反应上升时开始辅助免疫调节药物的给药,并且应限制其持续时间以减少不良影响。通过识别可靠的炎症生物标志物,可以优化这一关键时间框架。

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