Central nervous system and systemic inflammatory networks associated with acute neurological outcomes in COVID-19
Abstract COVID-19 is associated with a wide spectrum of neurological alterations, ranging from headache and dizziness to severe encephalopathy and inflammatory neurological diseases (IND), and neuropathological findings suggest immune-mediated processes. Therefore, we sought to characterize profiles...
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| Main Authors: | , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-07-01
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| Series: | Scientific Reports |
| Online Access: | https://doi.org/10.1038/s41598-025-08632-9 |
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| Summary: | Abstract COVID-19 is associated with a wide spectrum of neurological alterations, ranging from headache and dizziness to severe encephalopathy and inflammatory neurological diseases (IND), and neuropathological findings suggest immune-mediated processes. Therefore, we sought to characterize profiles of cytokines, chemokines, growth factors, and markers of central nervous system (CNS) homeostasis in COVID-19 patients with neurological alterations to identify key factors and mechanisms underlying CNS disturbances in COVID-19. The study included a case series of 52 COVID-19 patients with neurological manifestations, which were categorized into three groups: isolated refractory headache (n = 14), encephalopathy (n = 24), and IND (n = 14). Individuals with non-inflammatory, non-infectious neurological conditions (n = 9) were included as negative controls. Paired CSF and serum samples were assessed for 56 biomarkers. Regardless of the neurological condition, COVID-19 patients exhibited elevated CSF levels of proinflammatory mediators, including IL-2, IL-3, IL-6, IL-15, IL-25, IFN-α2, CCL7, CCL11, and GM-CSF. Patients with encephalopathy and IND also showed increased IL-1β, IL-18, TNF-α, neopterin, IL-7, CXCL8, CXCL9, TGF-α, EGF, sTREM-2, and HMGB1, consistent with a CNS cytokine storm. In contrast, individuals with isolated refractory headache showed a modest inflammatory profile, compatible with the limited CNS involvement. COVID-19 patients showed elevated serum IL-13, IL-18, TNF-α, VILIP-1, TGF-α, and VEGF levels, indicating systemic inflammation and potential blood–brain barrier (BBB) disruption. β-NGF was increased in the CSF of patients with encephalopathy and IND, suggesting the activation of neuroprotective responses during patient recovery. Functional protein network analysis showed a significant enrichment of interactions between factors altered in the CSF of patients with encephalopathy and IND, many of them related to processes of neuroinflammation and microglial functions, and leukocyte chemotaxis, activation and proliferation. These findings support a model in which both systemic immune activation and localized neuroinflammation contribute to the diversity of neurological outcomes observed in COVID-19, and dysregulated cytokine production, glial activation, inflammasome activity and BBB disturbances represent key factors in neuro-COVID-19 pathogenesis. |
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| ISSN: | 2045-2322 |