Mechanisms of Cholestatic Injury and Emerging Therapeutic Strategies

Description

This session explores the cellular and molecular drivers of cholestatic liver disease and emerging therapeutic strategies utilizing biliary gene therapy. Presentations examine the impact of impairments in biliary transport and signaling in promoting cholestatic injury, inflammation, and fibrosis.

Presentations

11:00 AM - 11:15 AM
Convention Center - Bluebird Ballroom 3DEF
Recorded session

Liver-Specific Tjp2 Deficiency in a Humanized Bile Acid Mouse Model Drives Cholestatic Injury via Immune Activation and Metabolic Suppression

Thi Hao Vu, PhD | Abstract Presenter
11:15 AM - 11:30 AM
Convention Center - Bluebird Ballroom 3DEF
Recorded session

Loss of biliary adherens junctions results in primary sclerosing cholangitis-like cholestatic injury

Vik Meadows, PhD | Abstract Presenter
11:30 AM - 11:45 AM
Convention Center - Bluebird Ballroom 3DEF
Recorded session

Biliary gene therapy

Pervin K Choksi, Bachelors | Abstract Presenter
11:45 AM - 12:00 PM
Convention Center - Bluebird Ballroom 3DEF
Recorded session

Engineering Injury-Resistant Functional Biliary Trees with Enhanced Drug Efflux Capacity

Shiwen Ma | Abstract Presenter
12:00 PM - 12:15 PM
Convention Center - Bluebird Ballroom 3DEF
Recorded session

Biliary cGAS-STING signaling mediates neutrophilic inflammation and fibrosis in cholestatic liver disease 

Mobin Ibne Mokbul, MD | Abstract Presenter
12:15 PM - 12:30 PM
Convention Center - Bluebird Ballroom 3DEF
Recorded session

Beyond Gilbert Syndrome: heterozygous UGT1A1 c.41_40dup defines a distinct cholangiopathic phenotype in young adults with Unexplained Chronic Cholestasis

Mario Romeo, MD | Abstract Presenter

Objectives

  • Describe how biliary junctional integrity and key signaling pathways drive cholestatic injury and fibrosis
  • Assess emerging regenerative and gene therapy strategies for treating cholestatic liver disease
  • Evaluate the use of mouse, organoid, and genetic models in studying cholestatic disease pathogenesis