Key result
Interplay between innate immunity and autophagy drives viral myocarditis and subsequent DCM development.
Why the study?
Viral myocarditis often progresses to dilated cardiomyopathy and heart failure, yet viable treatments remain elusive despite emerging evidence on innate immunity and autophagy crosstalk.
This review highlights the complex interplay between innate immunity and autophagy in the pathogenesis of viral myocarditis and its progression to dilated cardiomyopathy, suggesting potential therapeutic targets.
Identifies innate immunity-autophagy interplay as potential therapeutic targets in viral myocarditis; leaves open validation in prospective trials.
Viral myocarditis, characterised by inflammation of the heart muscle, presents a significant challenge to global public health, particularly affecting younger individuals and often progressing to dilated cardiomyopathy (DCM), a leading cause of heart failure. Despite ongoing research efforts, viable treatments for this condition remain elusive. Recent studies have shed light on the complex interplay between the innate immune response and autophagy mechanisms, revealing their pivotal roles in the pathogenesis of viral myocarditis and subsequent DCM development. This review aims to delve into the recent advancements in understanding the molecular mechanisms and pathways that intersect innate immunity and autophagy in the context of viral myocarditis. Furthermore, it explores the potential therapeutic implications of these findings, offering insights into promising avenues for the management and treatment of this debilitating condition.
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Wang et al. (2024) conducted a review in Viral myocarditis and dilated cardiomyopathy. The complex interplay between the innate immune response and autophagy mechanisms plays a pivotal role in the pathogenesis of viral myocarditis and subsequent dilated cardiomyopathy development.
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