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COVID-19 康复:新冠病毒感染后出现神经认知并发症患者的脑脊液生物标志物持续正常。

COVID-19 Recovery: Consistent Absence of Cerebrospinal Fluid Biomarker Abnormalities in Patients With Neurocognitive Post-COVID Complications.

机构信息

Department of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Department of Infectious Diseases, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

J Infect Dis. 2024 Feb 14;229(2):493-501. doi: 10.1093/infdis/jiad395.

DOI:10.1093/infdis/jiad395
PMID:37874918
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10873166/
Abstract

BACKGROUND

To investigate evidence of residual viral infection, intrathecal immune activation, central nervous system (CNS) injury, and humoral responses in cerebrospinal fluid (CSF) and plasma in patients recovering from coronavirus disease 2019 (COVID-19), with or without neurocognitive post-COVID condition (PCC).

METHODS

Thirty-one participants (25 with neurocognitive PCC) underwent clinical examination, lumbar puncture, and venipuncture ≥3 months after COVID-19 symptom onset. Healthy volunteers were included. CSF and plasma severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleocapsid and spike antigen (N-Ag, S-Ag), and CSF biomarkers of immune activation and neuronal injury were analyzed.

RESULTS

SARS-CoV-2 N-Ag or S-Ag were undetectable in all samples and no participant had pleocytosis. We detected no significant differences in CSF and plasma cytokine concentrations, albumin ratio, IgG index, neopterin, β2M, or in CSF biomarkers of neuronal injury and astrocytic damage. Furthermore, principal component analysis (PCA1) analysis did not indicate any significant differences between the study groups in the marker sets cytokines, neuronal markers, or anti-cytokine autoantibodies.

CONCLUSIONS

We found no evidence of ongoing viral replication, immune activation, or CNS injury in plasma or CSF in patients with neurocognitive PCC compared with COVID-19 controls or healthy volunteers, suggesting that neurocognitive PCC is a consequence of events suffered during acute COVID-19 rather than persistent viral CNS infection or residual CNS inflammation.

摘要

背景

为了研究从新冠病毒疾病 2019(COVID-19)中康复的患者(伴有或不伴有神经认知 COVID 后状况[PCC])的脑脊液(CSF)和血浆中是否存在残余病毒感染、鞘内免疫激活、中枢神经系统(CNS)损伤和体液反应的证据。

方法

31 名参与者(25 名患有神经认知 PCC)在 COVID-19 症状出现后至少 3 个月接受了临床检查、腰椎穿刺和静脉穿刺。纳入健康志愿者。分析 CSF 和血浆中严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)核衣壳和刺突抗原(N-Ag、S-Ag)以及 CSF 免疫激活和神经元损伤的生物标志物。

结果

所有样本中均未检测到 SARS-CoV-2 N-Ag 或 S-Ag,且无参与者出现白细胞增多。我们未发现 CSF 和血浆细胞因子浓度、白蛋白比值、IgG 指数、新蝶呤、β2M 或 CSF 神经元损伤和星形胶质细胞损伤生物标志物存在显著差异。此外,主成分分析(PCA1)分析未表明研究组之间在细胞因子、神经元标志物或抗细胞因子自身抗体的标志物组中有任何显著差异。

结论

与 COVID-19 对照组或健康志愿者相比,我们在伴有神经认知 PCC 的患者的血浆或 CSF 中未发现持续病毒复制、免疫激活或 CNS 损伤的证据,这表明神经认知 PCC 是急性 COVID-19 期间发生的事件的结果,而不是持续的病毒 CNS 感染或残留的 CNS 炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/10873166/f229bd655e91/jiad395f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/10873166/86dfdd09cb7b/jiad395f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/10873166/2da9ebeb8767/jiad395f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/10873166/f229bd655e91/jiad395f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/10873166/86dfdd09cb7b/jiad395f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/10873166/2da9ebeb8767/jiad395f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/10873166/f229bd655e91/jiad395f3.jpg

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本文引用的文献

1
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2
Post-acute sequelae of SARS-CoV-2 with clinical condition definitions and comparison in a matched cohort.新型冠状病毒感染后临床疾病定义及其在匹配队列中的比较。
Nat Commun. 2022 Oct 12;13(1):5822. doi: 10.1038/s41467-022-33573-6.
3
Persistent Circulating Severe Acute Respiratory Syndrome Coronavirus 2 Spike Is Associated With Post-acute Coronavirus Disease 2019 Sequelae.
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Neurol Neuroimmunol Neuroinflamm. 2025 Jan;12(1):e200356. doi: 10.1212/NXI.0000000000200356. Epub 2024 Dec 18.
4
Anti-Inflammatory and Neuroprotective Polyphenols Derived from the European Olive Tree, L., in Long COVID and Other Conditions Involving Cognitive Impairment.源自欧洲橄榄树的抗炎和神经保护多酚在长新冠和其他涉及认知障碍的疾病中的应用。
Int J Mol Sci. 2024 Oct 14;25(20):11040. doi: 10.3390/ijms252011040.
5
Cerebellitis following COVID-19 infection: A case-based systematic review and pooled analysis.新型冠状病毒肺炎感染后的小脑炎:基于病例的系统评价与汇总分析
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6
Blood Biomarkers of Long COVID: A Systematic Review.长新冠血液生物标志物:系统评价。
Mol Diagn Ther. 2024 Sep;28(5):537-574. doi: 10.1007/s40291-024-00731-z. Epub 2024 Aug 5.
7
Current clinical findings of acute neurological syndromes after SARS-CoV-2 infection.新型冠状病毒2感染后急性神经综合征的当前临床发现。
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8
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