Key result
Bidirectional innate and adaptive immune crosstalk drives MASLD pathogenesis.
Understanding the bidirectional interplay between innate and adaptive immune systems in MASLD may guide the development of novel therapeutics.
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May inform immune-targeted therapies for MASLD; leaves open prospective validation before clinical use.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is an unabated risk factor for end-stage liver diseases with no available therapies. Dysregulated immune responses are critical culprits of MASLD pathogenesis. Independent contributions from either the innate or adaptive arms of the immune system or their unidirectional interplay are commonly studied in MASLD. However, the bidirectional communication between innate and adaptive immune systems and its impact on MASLD remain insufficiently understood. Given that both innate and adaptive immune cells are indispensable for the development and progression of inflammation in MASLD, elucidating pathogenic contributions stemming from the bidirectional interplay between these two arms holds potential for development of novel therapeutics for MASLD. Here, we review the immune cell types and bidirectional pathways that influence the pathogenesis of MASLD and highlight potential pharmacologic approaches to combat MASLD based on current knowledge of this bidirectional crosstalk.
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Sawada et al. (2023) conducted a review in Metabolic dysfunction-associated steatotic liver disease (MASLD). Bidirectional immune crosstalk was evaluated. Bidirectional communication between innate and adaptive immune systems plays a critical role in the pathogenesis of metabolic dysfunction-associated steatotic liver disease.
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