4.7 Article

Microbiota Predict Infections and Acute Graft-Versus-Host Disease After Pediatric Allogeneic Hematopoietic Stem Cell Transplantation

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JOURNAL OF INFECTIOUS DISEASES
卷 -, 期 -, 页码 -

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OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiad190

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immunocompromised hosts; infections; microbiome; transplantation complications

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This study explores the correlation between gut microbiota and infection risk in pediatric allogeneic hematopoietic cell transplantation (allo-HCT). It finds that disruptions in the gut microbiome are related to infection risk in pediatric allo-HCT, and different microbiota patterns are associated with different infections. The ratios of specific bacteria types in the gut can predict the risk of bacteremia, bacterial infections, and viral enterocolitis.
Background Despite preventive measures, infections continue to pose significant risks to pediatric allogeneic hematopoietic cell transplantation (allo-HCT) recipients. The gut microbiota has been linked to clinical outcomes following adult allo-HCT. This study evaluated whether similar disruptions or differing microbiota patterns were associated with infection risk in pediatric allo-HCT. Methods In a prospective observational study, fecal samples were obtained from 74 children before conditioning and upon neutrophil recovery. Microbiome signatures identified through sequencing were examined for their associations with infections or acute graft-versus-host disease (aGVHD) in the first-year post-HCT using Cox proportional hazards analysis. Results Microbiome disruption in adults, did not predict infection risk in pediatric allo-HCT. Unique microbiota signatures were associated with different infections or aGVHD. A ratio of strict and facultative anaerobes (eg, Lachnoclostridium, Parabacteroides) prior to conditioning predicted bacteremia risk (Cox hazard ratio [HR], 3.89). A distinct ratio of oral (eg, Rothia, Veillonella) to intestinal anaerobes (eg, Anaerobutyricum, Romboutsia) at neutrophil recovery predicted likelihood of bacterial infections (Cox HR, 1.81) and viral enterocolitis (Cox HR, 1.96). Conclusions Interactions between medical interventions, pediatric hosts, and microbial communities contribute to microbiota signatures that predict infections. Further multicenter study is necessary to validate the generalizability of these ratios as biomarkers. Gut microbial communities can predict which children after hematopoietic cell transplantation will have infections or acute graft-versus-host disease. These ratios of gut community members can be used to focus prevention and treatment on children at highest risks for complications.

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