Neuroinflammatory disorders of the central nervous system associated with monkeypox virus: a systematic review and call to action

被引:0
|
作者
Deb, Shramana [1 ]
Mondal, Ritwick [1 ]
Sen, Purbita [1 ]
Chowdhury, Dipanjan [2 ]
Sarkar, Shramana [2 ]
Banerjee, Granthik [3 ]
Sarkar, Vramanti [4 ]
Chowdhury, Anjan [5 ]
Benito-Leon, Julian [6 ,7 ,8 ,9 ]
机构
[1] Inst Neurosci, Dept Stroke Med, Kolkata, India
[2] IPGMER & SSKM Hosp, Dept Internal Med, Kolkata, India
[3] Chittaranjan Natl Canc Inst CNCI, Dept Med Oncol, Kolkata, India
[4] Univ Calcutta, SN Pradhan Ctr Neurosci, Kolkata, India
[5] Indian Stat Inst, Dept Soft Comp, Kolkata, India
[6] Univ Hosp 12 Octubre, Dept Neurol, Madrid, Spain
[7] Inst Invest Sanit Hosp, 12 Octubre Imas12, Madrid, Spain
[8] Ctr Invest Biomed Red Enfermedades Neurodegenerat, Madrid, Spain
[9] Univ Complutense Madrid, Dept Med, Madrid, Spain
来源
BMC MEDICINE | 2025年 / 23卷 / 01期
基金
美国国家卫生研究院;
关键词
Monkeypox virus; Central nervous system; Neuroinflammatory disorders; Encephalitis; Encephalomyelitis; Meningoencephalitis; Transverse myelitis; qRT-PCR; Cerebrospinal fluid; Magnetic resonance imaging; Antiviral therapy; Immunomodulation; Systematic review; SMALLPOX;
D O I
10.1186/s12916-025-03921-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundMonkeypox virus (MPXV) has emerged as a significant global health concern with outbreaks worldwide. While MPXV is primarily known for its dermatological and systemic manifestations, it can also cause central nervous system (CNS) complications. This systematic review describes the demographic, clinical, diagnostic, and therapeutic characteristics of MPXV-associated CNS neuroinflammatory disorders.MethodsWe systematically reviewed the literature to identify cases of MPXV-associated CNS neuroinflammatory disorders. Data on demographics, systemic and neurological manifestations, diagnostic methods, treatment strategies, and outcomes were extracted and analyzed.ResultsEighteen cases of MPXV-associated neuroinflammatory disorders were identified. The mean age of patients was 27.8 years (range: 28 days to 43 years), with a male predominance (66.7%). Diagnosis included The most common diagnoses were acute disseminated encephalomyelitis in nine cases (50.0%), encephalitis/meningoencephalitis in seven cases (38.9%, isolated transverse myelitis in one case (5.6%), and transverse myelitis with encephalitis in one case (5.6%). The latency between the onset of systemic symptoms and neurological involvement averaged 6.2 days. MPXV detection was confirmed in 13 of 18 (72.2%) cases, primarily using quantitative real-time polymerase chain reaction from various biological specimens. Among the 12 cases with documented treatment, the most commonly administered therapies were tecovirimat (58.3%) and intravenous methyl-prednisolone (66.7%). Outcomes were reported in 17 cases, with complete recovery in 29.4%, partial recovery in 41.2%, and death in 29.4% of patients.ConclusionsMPXV-associated neuroinflammatory disorders of the CNS are rare but cause significant complications. The findings underscore the need for clinical vigilance, advanced diagnostic approaches, and targeted therapeutic strategies. Further research is essential to elucidate mechanisms underlying MPXV neurovirulence and develop effective treatments for these life-threatening conditions.
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页数:17
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