Para-infectious brain injury in COVID-19 persists at follow-up despite attenuated cytokine and autoantibody responses.



Michael, Benedict D ORCID: 0000-0002-8693-8926, Dunai, Cordelia ORCID: 0000-0001-5799-2387, Needham, Edward J ORCID: 0000-0001-7042-7462, Tharmaratnam, Kukatharmini ORCID: 0000-0002-8255-9822, Williams, Robyn ORCID: 0009-0000-9505-9563, Huang, Yun ORCID: 0000-0001-7843-9126, Boardman, Sarah A ORCID: 0000-0003-4385-6004, Clark, Jordan J, Sharma, Parul, Subramaniam, Krishanthi
et al (show 38 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-.

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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 and Life Sciences
Faculty of Health and Life Sciences > Institute of Infection, Veterinary and Ecological Sciences
Faculty of Health and Life Sciences > Institute of Population Health
Faculty of Health and Life Sciences > Institute of Systems, Molecular and Integrative Biology
Faculty of Health and Life Sciences > Tech, Infrastructure and Environmental Directorate
Depositing User: Symplectic Admin
Date Deposited: 02 Jan 2024 15:41
Last Modified: 12 Jan 2024 14:05
DOI: 10.1038/s41467-023-42320-4
Open Access URL: https://www.nature.com/articles/s41467-023-42320-4
Related URLs:
URI: https://livrepository.liverpool.ac.uk/id/eprint/3177687