# Comprehensive management of hematopoietic stem cell transplantation complications: from infection prevention to immune microenvironment reconstruction

**Authors:** Zhengrong Song, Xinzhi Han, Ziwei Zhou, Huan Hua, Fuxu Wang, Xuejun Zhang, Shupeng Wen

PMC · DOI: 10.3389/fimmu.2026.1740067 · Frontiers in Immunology · 2026-03-11

## TL;DR

This paper reviews strategies to manage complications in stem cell transplants, focusing on infections, GVHD, and VOD/SOS, and highlights new tools like AI and microbiome analysis for better patient outcomes.

## Contribution

The paper introduces emerging approaches such as AI and microbiome analysis for comprehensive HSCT complication management.

## Key findings

- Letermovir and post-transplant cyclophosphamide improve infection and GVHD control.
- Defibrotide and early biomarkers are critical for VOD/SOS management.
- Single-cell sequencing and AI can enhance risk management models for HSCT.

## Abstract

This article systematically reviews the management of key complications in hematopoietic stem cell transplantation (HSCT), including infections, graft-versus-host disease (GVHD), and hepatic sinusoidal obstruction syndrome (VOD/SOS). It highlights the importance of optimizing conditioning regimens to reduce infection risk and discusses the role of novel antiviral agents like letermovir in transforming infection control. For GVHD, the pathogenesis involving effector and regulatory T-cell imbalances is analyzed, together with prevention strategies such as post-transplant cyclophosphamide with antithymocyte globulin and TCRαβ/CD19 depletion. Ruxolitinib is emphasized for steroid-refractory GVHD, and gut microbiota modulation is noted as a promising intervention. For VOD/SOS, early biomarker detection and defibrotide treatment are critical. The review also explores the impact of immune reconstitution on infection control, GVHD development, and relapse, and examines how emerging approaches, including single-cell sequencing, microbiome analysis, and artificial intelligence, can be applied in building whole-course risk management models. Future directions include developing intelligent platforms and personalized strategies to enhance long-term patient outcomes.

## Linked entities

- **Chemicals:** letermovir (PubChem CID 45138674), cyclophosphamide (PubChem CID 2907), ruxolitinib (PubChem CID 17754772)
- **Diseases:** graft-versus-host disease (MONDO:0013730)

## Full-text entities

- **Genes:** CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}
- **Diseases:** infection (MESH:D007239), hepatic sinusoidal obstruction syndrome (MESH:D006504), GVHD (MESH:D006086)
- **Chemicals:** letermovir (MESH:C000588473), defibrotide (MESH:C036901), steroid (MESH:D013256), Ruxolitinib (MESH:C540383), cyclophosphamide (MESH:D003520)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13012925/full.md

## References

106 references — full list in the complete paper: https://tomesphere.com/paper/PMC13012925/full.md

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Source: https://tomesphere.com/paper/PMC13012925