# IFN‐γ Driven Hepatic Injury Exacerbates Mortality in NK/T‐Cell Lymphoma‐Associated Hemophagocytic Lymphohistiocytosis

**Authors:** Yehua Yu, Liyuan Ma, Haifang Hang, Yuyang Pang, Wei Lu, Jiajia Liu, Hui Zhou, Jun Shi

PMC · DOI: 10.1002/cam4.71606 · 2026-02-15

## TL;DR

This study shows that liver damage in a type of lymphoma called NK/T-cell lymphoma worsens survival, and targeting IFN-γ may help.

## Contribution

The study identifies the GSD index as a new prognostic tool and suggests anti-IFN-γ therapy for high-risk NK/T-HLH patients.

## Key findings

- All NK/T-HLH patients had elevated liver enzymes and bilirubin compared to those without HLH.
- The GSD index combining GGT, AST, and DBIL predicted mortality with high accuracy (AUC = 0.87).
- IFN-γ levels strongly correlated with liver injury markers and improved with anti-IFN-γ treatment.

## Abstract

Hepatic involvement is a life‐threatening complication in natural killer/T‐cell lymphoma with hemophagocytic lymphohistiocytosis (NK/T‐HLH). Nevertheless, the prognostic implications of hepatic dysfunction and its underlying related factors are not fully elucidated.

We retrospectively analyzed the clinical and laboratory data of 53 NK/T patients, comprising 35 cases without HLH and 18 with HLH. All NK/T‐HLH patients exhibited hepatic injury, characterized by significantly elevated hepatic enzyme levels and bilirubin compared to those without HLH (all p < 0.001). Glutamyltransferase (GGT), aspartate aminotransferase (AST), and direct bilirubin (DBIL) individually predicted mortality with AUC > 0.8 in NKTCL patients, while their composite GSD index enhanced predictive accuracy (AUC = 0.87).

Notably, NK/T‐HLH patients meeting the GSD index criteria had markedly reduced overall survival (OS) compared to non‐fulfillers (median OS: 2 vs 21 months; p = 0.003). Patients with hepatic involvement exhibited significantly higher levels of serum interferon‐γ(IFN‐γ) and interleukin‐10 (IL‐10). While, only IFN‐γ concentrations showed a strong positive correlation with the elevated levels of GGT, AST, and DBIL. To further validate the clinical relevance of these findings, we present two representative cases of NK/T‐HLH with severe hepatic injury. Both patients achieved rapid liver function recovery following a targeted regimen combining chemotherapy and emapalumab, a human anti‐IFN‐γ monoclonal antibody approved for primary HLH.

The GSD index emerges as a robust prognostic tool for NK/T‐HLH patients with hepatic dysfunction, reflecting underlying IFN‐γ‐mediated immunopathology. Early intervention with anti‐IFN‐γ monoclonal antibody may improve clinical outcomes in this high‐risk subgroup.

## Linked entities

- **Proteins:** IFNG (interferon gamma), IL10 (interleukin 10)
- **Diseases:** NK/T-cell lymphoma (MONDO:0019472), hemophagocytic lymphohistiocytosis (MONDO:0015540)

## Full-text entities

- **Genes:** IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, GGTLC5P (gamma-glutamyltransferase light chain 5 pseudogene) [NCBI Gene 653590] {aka GGT}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}
- **Diseases:** Hepatic Injury (MESH:D056486), NK/T (MESH:D001260), primary HLH (MESH:D010538), NK/T-Cell Lymphoma (MESH:D016399), GSD (MESH:D016098), NK/T-HLH (MESH:D000077428), hepatic dysfunction (MESH:D008107), Hemophagocytic Lymphohistiocytosis (MESH:D051359)
- **Chemicals:** DBIL (-), bilirubin (MESH:D001663), emapalumab (MESH:C000644327)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12906978/full.md

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Source: https://tomesphere.com/paper/PMC12906978