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