Signals Across Systems: Microbiome, Immunity, and Neuroinflammation in Liver Disorders

This session explores the complex, multisystem interactions that drive inflammation in liver disease, with a focus on gut-liver and liver-brain communication. Presentations highlight the roles of the microbiome in estrogen homeostasis, salivary and serum biomarkers in cirrhosis outcomes, and immune signaling pathways such as TLR8 and neutrophil recruitment in biliary and advanced liver disease. The session also delves into how hepatocyte-derived exosomes and β/γ-catenin signaling impact microbiome balance, intestinal inflammation, and neuroinflammation, underscoring new therapeutic opportunities at the interface of immunity and inter-organ communication.

Toward 2030: Collaborative Solutions for Hepatitis C Diagnosis, Care, and Elimination

This session presents innovative and collaborative approaches to achieving global Hepatitis C elimination for adults and children. Presenters will share insights on diagnostic strategies, care linkage, and progress toward the WHO 2030 targets, highlighting efforts across clinical, public health, and global contexts.

Cellular Signaling and Metabolic Regulation in Chronic Liver Disease

This session explores the intricate signaling pathways and metabolic networks that govern liver injury, repair, and chronic disease progression. Presentations will cover hepatocyte-stellate cell interactions, nuclear receptor signaling, autophagy zonation, and the molecular regulation of regeneration and fibrosis. Through multiomics and tissue-specific analyses, these studies illuminate how dysregulation of cellular communication and metabolism contributes to conditions such as steatohepatitis, fibrosis, sarcopenia, and Type II diabetes.

Cellular Catalysts of Fibrosis: Stromal Signals, Exosomes, and Inflammation in the Diseased Liver

This session highlights emerging mechanisms by which non-parenchymal cells (NPCs), particularly hepatic stellate cells (HSCs), orchestrate liver fibrogenesis in the context of metabolic dysfunction and chronic injury. Presentations will examine the impact of exosomal microRNAs, inflammasome activation, mitochondrial stress, and Notch/YAP signaling on HSC activation and fibrotic progression. Together, these studies illuminate how cell–cell communication, immune-metabolic crosstalk, and novel therapeutic targets shape liver fibrosis and hepatocellular carcinoma risk.

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