# Thrombomodulin protects against acute vascular and multiorgan injury in sickle cell disease

**Authors:** Guohui Ren, Dustin R. Fraidenburg, Suman Setty, Jiwang Chen, Janae Gonzales, Maria Armila Ruiz, Zalaya Ivy, Najmeh Eskandari, Richard D. Minshall, James P. Lash, Victor R. Gordeuk, Santosh L. Saraf

PMC · DOI: 10.1172/jci.insight.193884 · 2025-12-09

## TL;DR

Thrombomodulin protects against acute vascular and organ damage in sickle cell disease, with recombinant thrombomodulin showing potential to mitigate injury.

## Contribution

The study identifies thrombomodulin dysfunction as a novel contributor to multiorgan failure in sickle cell disease and proposes its therapeutic use.

## Key findings

- Reduced thrombomodulin function correlates with vascular and organ injury in SCD patients and mice.
- Recombinant thrombomodulin infusion restores blood flow and reduces injury biomarkers in mice.
- Thrombomodulin loss is linked to systemic vasculopathy in SCD-related multiorgan failure.

## Abstract

Vaso-occlusive episodes (VOEs) in the setting of hyperhemolysis can rapidly evolve into multiorgan failure in sickle cell disease (SCD). Although the mechanisms for rapid progression to multiorgan failure are unclear, a systemic vasculopathy with thrombotic microangiopathy–type features has been described. Reduced thrombomodulin (TM) function is implicated in some thrombotic microangiopathy syndromes. We observed a greater decline in platelet count and hemoglobin concentration and an increase in vascular injury biomarkers within 24 hours of admission for a VOE in 12 patients with SCD with multiorgan failure versus 12 patients without multiorgan failure. We observed decreased TM expression on the lung and kidney vasculature of 3 additional patients with SCD with multiorgan failure compared with a control patient without SCD. Transgenic SCD mice challenged with cell-free hemoglobin had reduced TM function, increased vascular injury biomarkers, and reduced renal cortical blood flow. Infusion of recombinant TM 2 or 24 hours after the challenge restored cortical blood flow and mitigated increases in vascular injury, complement activation, and tubular injury biomarkers, and protected against acute kidney and lung injury. We demonstrated that impaired TM function may be involved in the systemic vasculopathy of SCD-related multiorgan failure, and infusion of recombinant TM may restore vascular function and protect against acute organ damage.

In patients and transgenic sickle mice, thrombomodulin loss is associated with vascular, kidney, and lung injury and rescue with recombinant thrombomodulin mitigates the injury.

## Linked entities

- **Proteins:** MCL1 (MCL1 apoptosis regulator, BCL2 family member)
- **Diseases:** sickle cell disease (MONDO:0011382), multiorgan failure (MONDO:0043726), thrombotic microangiopathy (MONDO:0019737)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** THBD (thrombomodulin) [NCBI Gene 7056] {aka AHUS6, BDCA-3, BDCA3, CD141, THPH12, THRM}
- **Diseases:** acute organ damage (MESH:D000208), vascular and multiorgan injury (MESH:D057772), tubular injury (MESH:D000230), thrombotic microangiopathy (MESH:D057049), complement (MESH:D007153), Vaso-occlusive (MESH:D001157), SCD (MESH:D000755), systemic vasculopathy (MESH:C566007), multiorgan failure (MESH:D051437), acute kidney and lung injury (MESH:D055371)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12892889/full.md

---
Source: https://tomesphere.com/paper/PMC12892889