Selective cGAS inhibition is cardioprotective after myocardial infarction

Activation of the DNA sensor cGAS has emerged as a potential driver of maladaptive inflammation after myocardial infarction. In this study, the authors provide evidence that a newly developed pharmacologic cGAS inhibitor improves cardiac recovery following myocardial infarction. The compound, which can be administered orally, enhanced post-infarct cardiac function and attenuated adverse ventricular dilation. Using spatial transcriptomics, the authors further demonstrate that cGAS inhibition suppresses type I interferon signaling within the infarct border zone, accompanied by reduced expression of stress-associated cardiac remodeling markers such as Nppa. Together, these findings identify cGAS as a therapeutically targetable regulator of post-infarct inflammation and remodeling, and highlight the novelty of an orally bioavailable inhibitor capable of improving cardiac outcomes after myocardial injury.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-06-26
DOI
https://doi.org/10.5281/zenodo.20930205
Primary Topic
interferon and immune responses
Type
article
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article

Selective cGAS inhibition is cardioprotective after myocardial infarction

Van K. Ninh
Zenodo (CERN European Organization for Nuclear Research)
interferon and immune responses
article

Selective cGAS inhibition is cardioprotective after myocardial infarction

Van K. Ninh
article en

Abstract

Activation of the DNA sensor cGAS has emerged as a potential driver of maladaptive inflammation after myocardial infarction. In this study, the authors provide evidence that a newly developed pharmacologic cGAS inhibitor improves cardiac recovery following myocardial infarction. The compound, which can be administered orally, enhanced post-infarct cardiac function and attenuated adverse ventricular dilation. Using spatial transcriptomics, the authors further demonstrate that cGAS inhibition suppresses type I interferon signaling within the infarct border zone, accompanied by reduced expression of stress-associated cardiac remodeling markers such as Nppa. Together, these findings identify cGAS as a therapeutically targetable regulator of post-infarct inflammation and remodeling, and highlight the novelty of an orally bioavailable inhibitor capable of improving cardiac outcomes after myocardial injury.

Zenodo (CERN European Organization for Nuclear Research)
UC San Diego Health System (US)
Good health and well-being
Openalex Percentile: Top 10%
interferon and immune responses
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