Hematopoietic stem cell transplantation disrupts age-related gut microbiota signatures in pediatric and adult recipients - Scorecard - MDSpire

Hematopoietic stem cell transplantation disrupts age-related gut microbiota signatures in pediatric and adult recipients

  • By

  • Davide Leardini

  • Marcello Roberto

  • Sara Roggiani

  • Edoardo Muratore

  • Marco Fabbrini

  • Gianluca Storci

  • Enrica Tomassini

  • Elisa Dan

  • Angela Schipani

  • Serena De Matteis

  • Barbara Sinigaglia

  • Daria Messelodi

  • Nicola Salvatore Bertuccio

  • Arcangelo Prete

  • Patrizia Brigidi

  • Francesca Bonifazi

  • Riccardo Masetti

  • September 25, 2025

  • 0 min

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Clinical Scorecard: Hematopoietic Stem Cell Transplantation Alters Age-Related Gut Microbiome Profiles in Both Pediatric and Adult Patients

At a Glance

CategoryDetail
ConditionAllogeneic hematopoietic stem cell transplantation (allo-HSCT) and its impact on gut microbiome (GM)
Key MechanismsAlterations in gut microbiome diversity and composition influenced by age and transplant procedures; associations between GM signatures and clinical outcomes such as graft-versus-host disease (GvHD) and survival
Target PopulationPediatric and adult patients undergoing allo-HSCT
Care SettingAdult and pediatric transplant units in hospital setting

Key Highlights

  • Higher gut microbiome alpha diversity before transplant and at neutrophil engraftment correlates with improved overall survival and reduced GvHD-related mortality in adults.
  • Distinct gut microbiome signatures, including loss of beneficial taxa (e.g., Blautia) and overgrowth of pathogens (e.g., Enterococcus), are linked to increased risk of GvHD and infections.
  • Age influences gut microbiome composition and response to allo-HSCT, with pediatric patients experiencing larger microbiome shifts and more frequent myeloablative conditioning.

Guideline-Based Recommendations

Diagnosis

  • Assess gut microbiome diversity and composition before conditioning regimen and at neutrophil engraftment using stool samples and 16S rRNA sequencing.
  • Grade acute GvHD according to Mount Sinai Acute Gvhd International Consortium (MAGIC) criteria.

Management

  • Administer fluoroquinolone antibiotic prophylaxis starting at conditioning regimen until febrile neutropenia onset or neutrophil engraftment.
  • Consider age-related differences in conditioning intensity and microbiome disruption when planning transplant procedures.

Monitoring & Follow-up

  • Monitor neutrophil counts daily to define neutrophil engraftment (three consecutive days with neutrophils >0.5 × 10⁹/L).
  • Track gut microbiome changes longitudinally pre- and post-transplant to identify risk profiles for GvHD and infections.

Risks

  • Loss of gut microbiome diversity and beneficial commensals increases risk of GvHD and infection complications.
  • Overgrowth of opportunistic pathogens such as Enterococcus and Fusobacterium is associated with adverse outcomes.
  • Pediatric patients may experience greater microbiome disruption due to more frequent use of myeloablative conditioning.

Patient & Prescribing Data

Mixed cohort of pediatric and adult allo-HSCT recipients at a single hospital center.

Fluoroquinolone prophylaxis is standard; microbiome profiles differ by age and conditioning regimen intensity, influencing clinical outcomes.

Clinical Best Practices

  • Collect stool samples before conditioning and at neutrophil engraftment for microbiome analysis to guide risk stratification.
  • Implement shared antibiotic stewardship programs across adult and pediatric transplant units to optimize prophylaxis.
  • Use standardized criteria (MAGIC) for GvHD grading to ensure consistent outcome assessment.
  • Consider age-specific microbiome characteristics when interpreting microbiome data and planning interventions.

References

Original Source(s)

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