Alterations in Intestinal Microbiota, Metabolites, and Immune Cells in Allo-HSCT

Sponsor
The First Affiliated Hospital of Soochow University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06143501
Collaborator
(none)
250
1
52
4.8

Study Details

Study Description

Brief Summary

This research project delves into the critical role of gut immunity in the occurrence and progression of acute graft-versus-host disease (aGVHD) post allogeneic hematopoietic stem cell transplantation (allo-HSCT). Addressing the current gaps in understanding the involvement of intestinal microbiota, metabolites, and cellular metabolism in clinical aGVHD, the study involves comprehensive analyses on 200 allo-HSCT patients and 50 healthy volunteers. By scrutinizing changes in gut microbiota, metabolites, and immune cell metabolism, the research aims to shed light on their roles in allo-HSCT and their correlation with post-transplant complications. The findings are poised to offer crucial insights for diagnosing and prognosticating complications following transplantation.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Blood Sample
  • Diagnostic Test: Stool Sample
  • Diagnostic Test: Urine Sample

Detailed Description

The intestinal immune system plays a pivotal role in the onset, progression, and evolution of acute graft-versus-host disease (aGVHD) following allogeneic hematopoietic stem cell transplantation (allo-HSCT). However, the precise contributions and mechanisms underlying the involvement of intestinal microbiota, metabolites, and cellular metabolism in immune regulation during clinical aGVHD remain unclear.

This research initiative aims to collect peripheral blood, fecal, and urine samples from 200 patients before and after transplantation as well as 50 healthy volunteers. Comprehensive analyses, including metagenomics, 16S rRNA sequencing, transcriptomics, metabolomics, single-cell sequencing, as well as assessments of immune cell function and inflammatory cytokines, will be conducted. Additionally, longitudinal follow-up observations will be performed to monitor post-transplant complications, relapse and immune reconstitution.

By investigating the dynamics of gut microbiota, metabolites, and cellular metabolism and analyzing their correlation with changes in immune responses, this study seeks to elucidate the roles of intestinal microbiota, metabolites, and immune cell metabolism in the context of allo-HSCT. The findings are anticipated to provide insights into the correlation between these factors and outcomes of allo-HSCT patients, contributing valuable evidence for the diagnosis and prognosis assessment of complications following transplantation.

Study Design

Study Type:
Observational
Anticipated Enrollment :
250 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Alterations in Intestinal Microbiota, Metabolites, and Immune Cells Pre- and Post-Transplantation of Allogeneic Hematopoietic Stem Cells
Actual Study Start Date :
Sep 1, 2020
Anticipated Primary Completion Date :
Dec 31, 2024
Anticipated Study Completion Date :
Dec 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Allo-HSCT Recipients

Diagnostic Test: Blood Sample
6 ml blood (collection occurs once pre-transplantation and at three designated follow-up time points post-transplantation)

Diagnostic Test: Stool Sample
pea-sized amount (collection occurs once pre-transplantation and at three designated follow-up time points post-transplantation)

Diagnostic Test: Urine Sample
8 ml (collection occurs once pre-transplantation and at three designated follow-up time points post-transplantation)

Healthy Volunteers

Diagnostic Test: Blood Sample
6 ml blood (collection occurs once pre-transplantation and at three designated follow-up time points post-transplantation)

Diagnostic Test: Stool Sample
pea-sized amount (collection occurs once pre-transplantation and at three designated follow-up time points post-transplantation)

Diagnostic Test: Urine Sample
8 ml (collection occurs once pre-transplantation and at three designated follow-up time points post-transplantation)

Outcome Measures

Primary Outcome Measures

  1. Incidence of Complications [2 years]

    Recording and monitoring the occurrence of complications such as infection, GVHD, etc., documenting their onset time, type, severity, and management.

  2. Relapse [2 years]

    Documenting and monitoring the occurrence of relapse in study subjects, including recording the time of onset, severity, and management.

  3. Overall Survival [2 years]

    OS will be assessed from the first day of stem cells infused to death or last follow-up.

Secondary Outcome Measures

  1. Immune Function [Measured 3 months after stem cells infused]

    Incidence of neutrophil recovery; Incidence of lymphocyte and monocyte subset recovery

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients with hematologic disorders undergoing allo-HSCT.
Exclusion Criteria:
  • Patients with confirmed pathogenic intestinal infections and severe systemic infections at the time of sampling.

  • Diagnosis of autoimmune diseases, metabolic disorders, and chronic gastrointestinal diseases.

  • Pre-transplant diseases not in complete remission.

  • Post-transplant hematopoietic engraftment failure or pre-engraftment mortality.

Contacts and Locations

Locations

Site City State Country Postal Code
1 The First Affiliated Hospital of Soochow University Suzhou Jiangsu China 215000

Sponsors and Collaborators

  • The First Affiliated Hospital of Soochow University

Investigators

  • Study Chair: Yang Xu, M.D, The First Affiliated Hospital of Soochow University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
The First Affiliated Hospital of Soochow University
ClinicalTrials.gov Identifier:
NCT06143501
Other Study ID Numbers:
  • Pre-Post Allo-HSCT Monitoring
First Posted:
Nov 22, 2023
Last Update Posted:
Nov 22, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by The First Affiliated Hospital of Soochow University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 22, 2023