# Interferon‐gamma blocking as a promising treatment for severe liver dysfunction in secondary hemophagocytic lymphohistiocytosis after liver transplantation

**Authors:** Chen Chen, Tao Zhou, Jing Jin, Yi Luo, Lijing Shen, Qiang Xia, Yongbing Qian

PMC · DOI: 10.1002/jpr3.70126 · JPGN Reports · 2025-11-29

## TL;DR

Blocking interferon-gamma helped treat severe liver issues in a child with a rare post-transplant immune disorder, leading to full recovery.

## Contribution

Demonstrates the effectiveness of interferon-gamma blockade in treating HLH-related liver dysfunction after transplantation.

## Key findings

- Treatment with emapalumab reversed liver dysfunction and reduced inflammation in a pediatric patient.
- The patient showed complete clinical recovery without opportunistic infections after interferon-gamma blocking.
- Stable liver function and absence of EBV DNA were maintained for over 2 years post-treatment.

## Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a life‐threatening hyperinflammatory syndrome that can occur after solid organ transplantation but remains underrecognized in this setting. The diagnosis is often delayed due to overlapping clinical manifestations with infection, rejection, or malignancy, and management becomes particularly challenging when accompanied by severe hepatic dysfunction. Here, we describe a pediatric patient who developed Epstein–Barr virus (EBV)–associated secondary HLH following liver re‐transplantation for biliary atresia. On postoperative Day 10, the patient presented with high fever, cytopenia, hypertriglyceridemia, hypofibrinogenemia, and marked hyperferritinemia, accompanied by rapidly worsening liver injury. Bone marrow biopsy confirmed hemophagocytosis. Given the severe hepatic impairment and persistent inflammation, the patient received three doses of emapalumab (1 mg/kg), a monoclonal antibody blocking interferon‐γ, combined with corticosteroids, intravenous immunoglobulin, and antimicrobial prophylaxis. The treatment led to a rapid decline in ferritin levels, reversal of liver dysfunction, and complete clinical recovery without opportunistic infections. The patient has remained stable with normal liver function and negative EBV DNA for over 2 years of follow‐up. This case demonstrates that early interferon‐γ blockade can safely and effectively reverse HLH‐related liver injury after transplantation, offering a promising therapeutic strategy for the management of secondary HLH complicated by severe hepatic dysfunction.

## Linked entities

- **Diseases:** Hemophagocytic lymphohistiocytosis (MONDO:0015540), biliary atresia (MONDO:0008867)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** malignancy (MESH:D009369), opportunistic infections (MESH:D009894), hyperferritinemia (MESH:D000085583), infection (MESH:D007239), biliary atresia (MESH:D001656), hyperinflammatory syndrome (MESH:D013577), cytopenia (MESH:D006402), HLH (MESH:D051359), hepatic dysfunction (MESH:D008107), inflammation (MESH:D007249), hypertriglyceridemia (MESH:D015228), hypofibrinogenemia (MESH:D000347), fever (MESH:D005334), liver dysfunction (MESH:D017093)
- **Chemicals:** emapalumab (MESH:C000644327)
- **Species:** Homo sapiens (human, species) [taxon 9606], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376]

## Full text

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## Figures

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## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC12894085/full.md

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Source: https://tomesphere.com/paper/PMC12894085