The distribution of intestinal flora after hematopoietic stem cell transplantation in children

Author:

Tong Lin1ORCID,Meng Yan1,Zhang Luying1,Yu Jie1,Dou Ying1

Affiliation:

1. Department of Hematology Oncology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Chongqing Key Laboratory of Child Infection and Immunity Children's Hospital of Chongqing Medical University Chongqing China

Abstract

AbstractBackgroundThis prospective study aimed to comprehensively understand the changes in intestinal flora at different stages after hematopoietic stem cell transplantation (HSCT) in pediatric patients and to analyze the effect of intestinal flora on acute graft versus host disease (aGVHD), especially on gastrointestinal graft versus host disease (GI GVHD).MethodsA total of 32 children with primary diseases of primary immunodeficiency disease (PID) and thalassemia were included. 16S sequencing was used to characterize the microbiota layout at three time points peri‐transplant including pre‐transplant, Day +3, and Day +30.ResultsBy comparing the intestinal flora of children with GI GVHD and those without GI GVHD, it suggests that in children with GI GVHD, the distribution of intestinal flora after transplantation was more variable and more chaotic (chao1 index, Friedman test, p = .029). Besides, Veillonella and Ruminococcaceae were more abundant before transplantation, Bifidobacteriaceae and Bacillales were more abundant after transplantation. Comparing children with PID and thalassemia, it was found that the destruction of gut microbiota diversity was more significant in children with thalassemia after transplantation. The comparison of children with 0‐I° aGVHD and II‐III° aGVHD indicates that children with II‐III° aGVHD had more Bilophila before transplantation than children with 0‐I° aGVHD. Additionally, exploratory analyses to evaluate correlations between clinical characteristics (medications, immune cell recovery, etc.) and microbiome features were also performed.ConclusionsThis study has synthetically shown the distribution of intestinal flora after allo‐HSCT, and some characteristic bacteria at different stages that may serve as potential biomarkers were screened out additionally, perhaps providing clues for the prevention and treatment of the disease.

Publisher

Wiley

Subject

Transplantation,Pediatrics, Perinatology and Child Health

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