Evidence map›Paper›PMID 41409593›Full record

ArticleClinical & translational immunology2025

Elevated plasma CXCL9 and CHI3L1 prior to HCT predict post-HCT lung complications in children.

Hannah Walker, Liam Gubbels, Gabrielle M Haeusler, Shivanthan Shanthikumar, Diane Hanna, Theresa Cole, Melanie R Neeland

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Article in Clinical & translational immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Hannah WalkerChildren's Cancer Centre Royal Children's Hospital Parkville VIC Australia.
Liam GubbelsMurdoch Children's Research Institute Parkville VIC Australia.
Gabrielle M HaeuslerDepartment of Paediatrics University of Melbourne Parkville VIC Australia.
Shivanthan ShanthikumarDepartment of Paediatrics University of Melbourne Parkville VIC Australia.ORCID https://orcid.org/0000-0001-6000-3180
Diane HannaChildren's Cancer Centre Royal Children's Hospital Parkville VIC Australia.
Theresa ColeChildren's Cancer Centre Royal Children's Hospital Parkville VIC Australia.
Melanie R NeelandDepartment of Paediatrics University of Melbourne Parkville VIC Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Lung complications occur commonly post-haematopoietic stem cell transplant (HCT) in children and contribute significantly to mortality. The development of biomarkers predictive of post-HCT lung complications may improve outcomes for these children. Therefore, the primary objective of this study was to identify pre-transplant plasma biomarkers predictive of lung complications in children undergoing HCT. Methods: Plasma samples from 117 pre-HCT patients were used to measure 78 soluble immune analytes, and extensive clinical metadata were retrospectively collected from the electronic medical record, including clinical characteristics of the post-HCT lung complications. Results: Firstly, we showed that the plasma cytokine signature of children undergoing HCT differed significantly between children depending on the indication for HCT (malignant vs non-malignant). Secondly, we found that the plasma cytokine signature changed with the age of the patient. Thirdly, we showed that elevated pre-HCT plasma levels of CXCL9 and Chitinase 3-like 1, both induced by IFN-γ, were predictive of post-HCT lung complications in patients with a malignant indication for HCT [area under the curve (AUC): 0.70, Conclusion: In conclusion, we have identified two potential biomarkers of post-HCT lung disease in paediatric patients and these require validation in future cohorts.

Indexed as

biomarkerCHI3L1CXCL9haematopoietic stem cell transplantpaediatricpulmonary complications

Identifiers

PMID41409593
PMCPMC12707545

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