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Long-term Elevation of Complement Factors in Cerebrospinal Fluid of Patients With Borna Disease Virus 1 Encephalitis.

Authors :
Bauswein, Markus
Zoubaa, Saida
Toelge, Martina
Eidenschink, Lisa
Riemenschneider, Markus J
Neumann, Bernhard
Lee, De-Hyung
Eid, Ehab
Tappe, Dennis
Niller, Hans Helmut
Gessner, André
Schmidt, Barbara
Bülow, Sigrid
Angstwurm, Klemens
Source :
Journal of Infectious Diseases. 10/15/2024, Vol. 230 Issue 4, pe943-e953. 11p.
Publication Year :
2024

Abstract

Background Borna disease virus 1 (BoDV-1) causes rare but severe zoonotic infections in humans, presenting as encephalitis. The case-fatality risk is very high and no effective countermeasures have been established so far. An immunopathology is presumed, while data on immune responses in humans are limited. Evidence of a role of the complement system in various neurological disorders and in viral infections of the central nervous system is increasing and specific inhibitors are available as therapeutic options. Methods In this study, we investigated factors of the complement system in the cerebrospinal fluid (CSF) of patients with BoDV-1 infections (n = 17) in comparison to noninflammatory control CSF samples (n = 11), using a bead-based multiplex assay. In addition, immunohistochemistry was performed using postmortem brain tissue samples. Results We found an intrathecal elevation of complement factors of all complement pathways and an active cascade during human BoDV-1 infections. The increase of certain complement factors such as C1q was persistent, and C3 complement deposits were detected in postmortem brain sections. Intrathecal complement levels were negatively correlated with survival. Conclusions Further investigations are warranted to clarify whether targeting the complement cascade by specific inhibitors might be beneficial for patients suffering from severe BoDV-1 encephalitis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00221899
Volume :
230
Issue :
4
Database :
Academic Search Index
Journal :
Journal of Infectious Diseases
Publication Type :
Academic Journal
Accession number :
180302159
Full Text :
https://doi.org/10.1093/infdis/jiae183