Evaluation of triumeq treatment on a TDP-43 mouse model of amyotrophic Lateral sclerosis

and inflammatory marker expression. Mice were treated with Triumeq and TDP-43 pathology and inflammatory marker expression examined. Triumeq treatment significantly improved motor function early on in the disease course but did not impact other disease progression markers or disease endpoint. In this TDP-43 ALS mouse model, there was a positive association of TDP-43 mRNA levels with transcription factor ATF4, and inflammatory markers CXCL10 and IRF-1, and Triumeq treatment negated this association. Triumeq treatment transiently and modestly improved motor function and influenced TDP-43 associated inflammatory gene expression in an ALS mouse model. These findings support the potential use of Triumeq in treating TDP-43-associated ALS and supports further investigation to better understand if the beneficial actions of Triumeq are via disruption of TDP-43-driven inflammation in ALS.

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Publication Details

Journal
Scientific Reports
Published
2026-05-27
DOI
https://doi.org/10.1038/s41598-026-55433-9
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Evaluation of triumeq treatment on a TDP-43 mouse model of amyotrophic Lateral sclerosis

Mary‐Louise Rogers, Jillian M. Carr, Julian Gold, Adam Walker et al.
Scientific Reports
Amyotrophic Lateral Sclerosis Research
article

Evaluation of triumeq treatment on a TDP-43 mouse model of amyotrophic Lateral sclerosis

Mary‐Louise Rogers, Jillian M. Carr, Julian Gold, Adam Walker, Megan Fowler
article en

Abstract

and inflammatory marker expression. Mice were treated with Triumeq and TDP-43 pathology and inflammatory marker expression examined. Triumeq treatment significantly improved motor function early on in the disease course but did not impact other disease progression markers or disease endpoint. In this TDP-43 ALS mouse model, there was a positive association of TDP-43 mRNA levels with transcription factor ATF4, and inflammatory markers CXCL10 and IRF-1, and Triumeq treatment negated this association. Triumeq treatment transiently and modestly improved motor function and influenced TDP-43 associated inflammatory gene expression in an ALS mouse model. These findings support the potential use of Triumeq in treating TDP-43-associated ALS and supports further investigation to better understand if the beneficial actions of Triumeq are via disruption of TDP-43-driven inflammation in ALS.

Scientific Reports
The University of Sydney (AU), The University of Queensland (AU), Flinders University (AU), Flinders Medical Centre (AU), Cooperative Trials Group for Neuro-Oncology (AU), Adelaide Institute for Sleep Health (AU), Perron Institute for Neurological and Translational Science (AU), Macquarie University (AU)
Motor Neurone Disease Research Australia
Good health and well-being
Openalex Percentile: Top 6%
Amyotrophic Lateral Sclerosis Research
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