Null effects of C5 inhibition on functional and tissue outcomes after traumatic brain injury in mice

The complement system plays a critical role in the pathophysiology of traumatic brain injury (TBI). This study examined the effects of complement component C5 inhibition on functional recovery, edema formation, and histopathological outcomes following moderate TBI. Male C57BL/6 mice received the monoclonal anti-C5 antibody BB5.1 or an isotype control antibody two hours before TBI induction as induced using controlled cortical impact (CCI), with a second dose given four days post-injury. Functional outcomes were assessed at 2 and 24 h, and on days 3, and 7 post-injury. Histopathological evaluations were carried out on day 1 and 7, and post-mortem magnetic resonance imaging was used on day 7 to quantify edema and lesion volumes. In summary, no significant differences in neurological deficits were observed in mice treated with BB5.1 in both the short-term and longer-term experiment. Furthermore, no difference in edema and lesion volume was observed in both the histopathological analyses and MRI data.

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Publication Details

Journal
Discover Neuroscience
Published
2026-06-30
DOI
https://doi.org/10.1186/s13064-026-00289-y
Primary Topic
Complement system in diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Null effects of C5 inhibition on functional and tissue outcomes after traumatic brain injury in mice

Tatjana Starzetz, Ferdinand O. Bohmann, Dan Carlin, Sarah Gelhard et al.
Discover Neuroscience
Complement system in diseases
article

Null effects of C5 inhibition on functional and tissue outcomes after traumatic brain injury in mice

Tatjana Starzetz, Ferdinand O. Bohmann, Dan Carlin, Sarah Gelhard, Franziska Lieschke, Dominic Menger, Amit Mogha, Michelle Rosenthal-Rueckeis, Christian Grefkes
article en

Abstract

The complement system plays a critical role in the pathophysiology of traumatic brain injury (TBI). This study examined the effects of complement component C5 inhibition on functional recovery, edema formation, and histopathological outcomes following moderate TBI. Male C57BL/6 mice received the monoclonal anti-C5 antibody BB5.1 or an isotype control antibody two hours before TBI induction as induced using controlled cortical impact (CCI), with a second dose given four days post-injury. Functional outcomes were assessed at 2 and 24 h, and on days 3, and 7 post-injury. Histopathological evaluations were carried out on day 1 and 7, and post-mortem magnetic resonance imaging was used on day 7 to quantify edema and lesion volumes. In summary, no significant differences in neurological deficits were observed in mice treated with BB5.1 in both the short-term and longer-term experiment. Furthermore, no difference in edema and lesion volume was observed in both the histopathological analyses and MRI data.

Discover NeuroscienceVol. 21(1)
Goethe University Frankfurt (DE), Alexion Pharmaceuticals (United States) (US), University Hospital Frankfurt (DE), AstraZeneca (United States) (US), Georg Speyer Haus (DE), Charité - Universitätsmedizin Berlin (DE)
AstraZeneca, Alexion Pharmaceuticals
Good health and well-being
Openalex Percentile: Top 11%
Complement system in diseases
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