Human Cytomegalovirus Associated Neuropathies: A Comprehensive Review From Pathophysiology to Clinical and Therapeutic Considerations

IF 3 3区 医学 Q1 CLINICAL NEUROLOGY
Naomi Behanan, Sarab Mohamed, Rhona Chen, Gloria Mak, Jian-Qiang Lu
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引用次数: 0

Abstract

Human cytomegalovirus (HCMV) is a neurotropic, double-stranded DNA virus from the Herpesviridae family. It has a large genome, infects the majority of populations, and typically causes asymptomatic infections in healthy individuals. After the initial infection with established lifelong latency, HCMV can reactivate and cause disorders including neuropathies. Besides the infections typically in immunocompromised patients, HCMV may also trigger autoimmunity leading to tissue injury and associated pathologies. HCMV-associated neuropathies are a pathogenically heterogeneous group of peripheral nervous system (PNS) disorders that include direct HCMV infection of the nerve(s), as well as non-infectious associated neuropathies such as axonal or degenerative, vasculitic/ischemic or necrotizing, inflammatory demyelinating, and immune-mediated forms. Congenital HCMV-associated neuropathies primarily involve the cochlear/auditory and optic nerves with somewhat distinct pathogenic mechanisms compared with their postnatal counterparts, largely due to the immaturity of the fetal immune system. This article reviews the pathophysiology of PNS involvement in HCMV infection, followed by congenital HCMV-associated neuropathies with a case demonstration, and various postnatal HCMV-associated neuropathies, including a detailed review of HCMV-associated optic neuropathies, from pathogenic mechanisms to clinical and therapeutic implications. As the PNS has a few immune protective mechanisms against pathogens, direct HCMV infection of nerves is rare and occurs only in immunocompromised patients; most HCMV-associated neuropathies are secondary with multiple pathogenic mechanisms including varying degrees of autoimmunity. While the clinical manifestations of HCMV-associated neuropathies are variable, their treatment is typically empirical and case-based, focusing on antiviral therapy often combined with immunomodulatory approaches. Prompt and appropriate management can improve outcomes of HCMV-associated neuropathies.

Abstract Image

人类巨细胞病毒相关神经病变:从病理生理学到临床和治疗考虑的综合综述。
人巨细胞病毒(HCMV)是疱疹病毒科的一种嗜神经双链DNA病毒。它有一个大的基因组,感染大多数人群,并且通常在健康个体中引起无症状感染。初次感染具有确定的终身潜伏期后,HCMV可重新激活并引起包括神经病变在内的疾病。除了免疫功能低下患者的典型感染外,HCMV还可能引发自身免疫,导致组织损伤和相关病理。HCMV相关神经病是一组病理异质性的外周神经系统(PNS)疾病,包括直接感染神经的HCMV,以及非感染性相关神经病,如轴突或退行性、血管/缺血性或坏死性、炎症性脱髓鞘和免疫介导形式。先天性hcmv相关的神经病变主要涉及耳蜗/听觉和视神经,与出生后的病变相比,其致病机制有所不同,主要是由于胎儿免疫系统不成熟。本文综述了PNS参与HCMV感染的病理生理学,随后是先天性HCMV相关神经病的病例论证,以及各种出生后HCMV相关神经病,包括HCMV相关视神经病变的详细综述,从致病机制到临床和治疗意义。由于PNS对病原体的免疫保护机制很少,因此HCMV直接感染神经是罕见的,仅发生在免疫功能低下的患者中;大多数hcmv相关的神经病变是继发性的,具有多种致病机制,包括不同程度的自身免疫。虽然hcmv相关神经病变的临床表现是可变的,但其治疗通常是经验和病例为基础的,重点是抗病毒治疗,通常结合免疫调节方法。及时和适当的治疗可以改善hcmv相关神经病变的预后。
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来源期刊
CiteScore
6.10
自引率
7.90%
发文量
45
审稿时长
>12 weeks
期刊介绍: The Journal of the Peripheral Nervous System is the official journal of the Peripheral Nerve Society. Founded in 1996, it is the scientific journal of choice for clinicians, clinical scientists and basic neuroscientists interested in all aspects of biology and clinical research of peripheral nervous system disorders. The Journal of the Peripheral Nervous System is a peer-reviewed journal that publishes high quality articles on cell and molecular biology, genomics, neuropathic pain, clinical research, trials, and unique case reports on inherited and acquired peripheral neuropathies. Original articles are organized according to the topic in one of four specific areas: Mechanisms of Disease, Genetics, Clinical Research, and Clinical Trials. The journal also publishes regular review papers on hot topics and Special Issues on basic, clinical, or assembled research in the field of peripheral nervous system disorders. Authors interested in contributing a review-type article or a Special Issue should contact the Editorial Office to discuss the scope of the proposed article with the Editor-in-Chief.
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