Related Experiment Video
Updated: Jun 3, 2025

Optimized Analysis of In Vivo and In Vitro Hepatic Steatosis
Published on: March 11, 2017
Pharmacotherapy of Liver Fibrosis and Hepatitis: Recent Advances
Liangtao Zhao1, Haolan Tang2, Zhangjun Cheng1
1Hepato-Pancreato-Biliary Center, Zhongda Hospital, School of Medicine, Southeast University, Nanjing 210009, China.
Abstract:
Liver fibrosis is a progressive scarring process primarily caused by chronic inflammation and injury, often closely associated with viral hepatitis, alcoholic liver disease, metabolic dysfunction-associated steatotic liver disease (MASLD), drug-induced liver injury, and autoimmune liver disease (AILD). Currently, there are very few clinical antifibrotic drugs available, and effective targeted therapy is lacking. Recently, emerging antifibrotic drugs and immunomodulators have shown promising results in animal studies, and some have entered clinical research phases. This review aims to systematically review the molecular mechanisms underlying liver fibrosis, focusing on advancements in drug treatments for hepatic fibrosis. Furthermore, since liver fibrosis is a progression or endpoint of many diseases, it is crucial to address the etiological treatment and secondary prevention for liver fibrosis. We will also review the pharmacological treatments available for common hepatitis leading to liver fibrosis.
Insights
This review explores liver fibrosis, a scarring condition linked to various liver diseases. It highlights new antifibrotic drugs and treatments for underlying causes and common hepatitis, offering hope for better therapeutic strategies.
Area of Science:
- Hepatology and Pharmacology
- Immunology and Molecular Biology
Background:
- Liver fibrosis is a significant scarring process resulting from chronic inflammation and injury.
- It is associated with prevalent conditions like viral hepatitis, alcoholic liver disease, and metabolic dysfunction-associated steatotic liver disease (MASLD).
- Current antifibrotic therapies are limited, with a lack of effective targeted treatments.
Purpose of the Study:
- To systematically review the molecular mechanisms driving liver fibrosis.
- To focus on recent advancements in drug treatments for hepatic fibrosis.
- To discuss etiological treatments, secondary prevention, and pharmacological options for common hepatitis leading to fibrosis.
Main Methods:
- Systematic literature review of molecular mechanisms.
- Analysis of preclinical and clinical data on emerging antifibrotic drugs and immunomodulators.
- Review of pharmacological treatments for hepatitis and liver fibrosis.
Main Results:
- Emerging antifibrotic drugs and immunomodulators show promise in preclinical studies.
- Some novel therapies have progressed to clinical research phases.
- A comprehensive understanding of molecular mechanisms is crucial for targeted treatment development.
Conclusions:
- Targeted antifibrotic therapies and immunomodulators represent a promising frontier for liver fibrosis treatment.
- Addressing the root causes of liver injury and implementing secondary prevention are vital.
- Further research and clinical trials are necessary to translate preclinical findings into effective patient care.
Related Concept Videos
Liver Regeneration
Cells of Liver
The liver comprises four major types of cells— hepatocytes, stellate, Kupffer, and sinusoidal endothelial cells. The hepatocytes are...
Inflammatory Bowel Disease IV: Pharmacological Management
Pharmacologic...
Targeted Cancer Therapies
There are several types of targeted therapies against...

