# Novel strategies to accelerate repair of drug-induced hepatotoxicity

> **NIH NIH R01** · MICHIGAN STATE UNIVERSITY · 2024 · $537,217

## Abstract

PROJECT SUMMARY
Acute liver injury caused by overdose of the pain medication acetaminophen (APAP) is a leading cause of
acute liver injury in the United States. In many cases, a failure of liver repair causes acute liver injury to persist
and this can progress to acute liver failure (ALF). Acute liver injury and ALF have a poor prognosis and little
therapeutic options beyond intensive care. Over the past decade, several studies have highlighted how
changes in the hemostatic system are connected to the progression of ALF. For example, an unbalance in the
platelet adhesive protein von Willebrand Factor (VWF) and its primary regulatory enzyme ADAMTS13 have
been identified as unique indicators of increased risk for liver transplant and death in patients with ALF. Our
published studies indicate that VWF inhibits repair of the APAP-injured liver. Strong preliminary results using
mice with deficiencies in VWF or ADAMTS13, leading-edge VWF-targeted therapeutics, and human ALF
samples suggest that VWF inhibits the resolution of APAP-induced liver injury. Based on our published and
preliminary studies, our central hypothesis is that hepatic VWF deposition inhibits the resolution of APAP-
induced liver injury through formation of intrahepatic VWF-platelet microthrombi. Our approach includes
genetically-modified mice, VWF-targeted molecules in clinical development, novel molecules designed to hold
VWF in a resting state, and novel VWF-targeted thrombolytic drugs. These studies are closely aligned with
creative analyses in which we seek to uncover VWF-focused biomarkers as novel biomarkers of liver repair
and outcome in samples from a large, well-characterized cohort provided by the ALF Study Group. The
investigative team represents an optimal pairing of experts on hemostasis and liver disease, experts on VWF
and thrombolysis, and highly collaborative physician-scientists, increasing the impact of our studies and
potential for translation. Our proposed studies will determine the role of ADAMTS13 and VWF multimer size in
APAP-induced liver injury and repair (Aim 1), determine the mechanisms linking VWF to inhibition liver repair
after APAP challenge (Aim 2), and identify strategies to accelerate degradation of pathologic VWF deposits to
enhance repair of the APAP-injured liver (Aim 3). The expected outcome of these Specific Aims is the
discovery of novel mechanisms whereby VWF inhibits repair of the injured liver. This outcome would make a
significant impact on the field because it would deliver novel mechanistic details for clinical associations
between VWF and poor outcome in acute liver injury. The proposed studies are transformative and anticipated
to deliver clinically applicable strategies to accelerate repair of the liver, owing to a strong combination of
experimental and translational science backed by a team with clinical and basic research expertise.

## Key facts

- **NIH application ID:** 10872235
- **Project number:** 5R01DK136733-02
- **Recipient organization:** MICHIGAN STATE UNIVERSITY
- **Principal Investigator:** James P Luyendyk
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $537,217
- **Award type:** 5
- **Project period:** 2023-07-01 → 2028-04-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10872235

## Citation

> US National Institutes of Health, RePORTER application 10872235, Novel strategies to accelerate repair of drug-induced hepatotoxicity (5R01DK136733-02). Retrieved via AI Analytics 2026-05-30 from https://api.ai-analytics.org/grant/nih/10872235. Licensed CC0.

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