Michael, BD
ORCID: 0000-0002-8693-8926, Dunai, C
ORCID: 0000-0001-5799-2387, Needham, EJ
ORCID: 0000-0001-7042-7462, Tharmaratnam, K
ORCID: 0000-0002-8255-9822, Williams, R
ORCID: 0009-0000-9505-9563, Huang, Y
ORCID: 0000-0001-7843-9126, Boardman, SA
ORCID: 0000-0003-4385-6004, Clark, JJ, Sharma, P
ORCID: 0000-0002-9090-7540, Subramaniam, K et al (show 88 more authors)
(2023)
Para-infectious brain injury in COVID-19 persists at follow-up despite attenuated cytokine and autoantibody responses
Nature Communications, 14 (1).
8487-.
ISSN 2041-1723, 2041-1723
Abstract
To understand neurological complications of COVID-19 better both acutely and for recovery, we measured markers of brain injury, inflammatory mediators, and autoantibodies in 203 hospitalised participants; 111 with acute sera (1–11 days post-admission) and 92 convalescent sera (56 with COVID-19-associated neurological diagnoses). Here we show that compared to 60 uninfected controls, tTau, GFAP, NfL, and UCH-L1 are increased with COVID-19 infection at acute timepoints and NfL and GFAP are significantly higher in participants with neurological complications. Inflammatory mediators (IL-6, IL-12p40, HGF, M-CSF, CCL2, and IL-1RA) are associated with both altered consciousness and markers of brain injury. Autoantibodies are more common in COVID-19 than controls and some (including against MYL7, UCH-L1, and GRIN3B) are more frequent with altered consciousness. Additionally, convalescent participants with neurological complications show elevated GFAP and NfL, unrelated to attenuated systemic inflammatory mediators and to autoantibody responses. Overall, neurological complications of COVID-19 are associated with evidence of neuroglial injury in both acute and late disease and these correlate with dysregulated innate and adaptive immune responses acutely.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | ISARIC4C Investigators, COVID-CNS Consortium, Humans, Brain Injuries, Glial Fibrillary Acidic Protein, Inflammation Mediators, Autoantibodies, Cytokines, Follow-Up Studies, Biomarkers, COVID-19, COVID-19 Serotherapy |
| Divisions: | Faculty of Health & Life Sciences Faculty of Health & Life Sciences > Inst. Infection, Vet & Ecological Sciences Faculty of Health & Life Sciences > Inst. Population Health Faculty of Health & Life Sciences > Inst. Systems, Molec & Integrative Biology > Inst. Systems, Molec & Integrative Biology Faculty of Health & Life Sciences > Tech, Infrastructure & Env Directorate |
| Depositing User: | Symplectic Admin |
| Date Deposited: | 02 Jan 2024 15:41 |
| Last Modified: | 22 Jan 2026 08:42 |
| DOI: | 10.1038/s41467-023-42320-4 |
| Open Access URL: | https://www.nature.com/articles/s41467-023-42320-4 |
| Related Websites: | |
| URI: | https://livrepository.liverpool.ac.uk/id/eprint/3177687 |
| Disclaimer: | The University of Liverpool is not responsible for content contained on other websites from links within repository metadata. Please contact us if you notice anything that appears incorrect or inappropriate. |
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