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Analysis of Intestinal Defensin Expression in Acute GVHD

Analysis of Intestinal Defensin Expression in Patients With Acute Graft-versus-Host Disease (GVHD)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04522843
Enrollment
80
Registered
2020-08-21
Start date
2018-09-01
Completion date
2024-10-30
Last updated
2024-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

GVHD,Acute, Morbus Crohn, Ulcerative Colitis

Brief summary

This study has the aim to analyze intestinal expression of endogenous antimicrobial peptides in patients with acute GVHD. The expression will be compared to intestinal expression of defensins in patients with colitis and patients without intestinal inflammation.

Detailed description

Acute graft-versus-host disease (GVHD) is a major cause of morbidity and mortality in patients undergoing allogeneic hematopoietic cell transplantation (allo-HCT). Acute GVHD is characterized by complex deficiencies of the mucosal antimicrobial barrier and intestinal dysbiosis, which contribute to disease pathogenesis. Defensins are endogenous epithelial cell-derived antimicrobial peptides, which can protect epithelial barrier integrity, shape the intestinal microbiota composition and contribute to host immunoregulation. Deregulated expression of defensins has been reported in patients with colitis, including Chron's Disease and ulcerative colitis. In this study, the investigators aim to analyze the expression of defensins in the intestine of patients with acute GVHD to study whether it is deregulated. The results will be valuable to study the role of defensins during acute GVHD pathogenesis or as potential biomarkers for disease activity.

Interventions

None listed

Sponsors

University of Freiburg
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* age ≥ 18 years * diagnostic endoscopy was performed * diagnosis results available * written informed consent * ability to understand the nature of the study and the study related procedures and to comply with them

Exclusion criteria

* age \< 18 years * gastrointestinal cancer * lack of informed consent

Design outcomes

Primary

MeasureTime frameDescription
Defensin Expression (mRNA)3 yearsAnalysis of alpha-defensin and beta-defensin mRNA expression by realtime PCR (qRT-PCR)
Defensin Expression (peptide)3 yearsAnalysis of alpha-defensin and beta-defensin levels by immunohistochemistry

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026