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Updated: Sep 14, 2025

Bone Marrow Transplantation Platform to Investigate the Role of Dendritic Cells in Graft-versus-Host Disease
Published on: March 17, 2020
Decreased HLA-DR+CD3+ T cells three months after allogeneic stem cell transplantation predict severe chronic GvHD and
Stefan Koeck1, Gabriele Hetzenauer1, Ines Peschel-Schaar2
1Department of Internal Medicine V, Medical University of Innsbruck, Anichstraße 35, 6020 Innsbruck, Tyrol, Austria.
Insights
Low peripheral blood activated T cells after allogeneic hematopoietic stem cell transplantation (HSCT) indicate a higher risk for transplant-related mortality (TRM) and chronic graft-versus-host disease (cGvHD). This finding may help identify high-risk patients early.
Area of Science:
- Immunology
- Transplantation Medicine
- Biomarker Discovery
Background:
- Chronic graft-versus-host disease (cGvHD) is a significant factor in transplant-related mortality (TRM) following allogeneic hematopoietic stem cell transplantation (HSCT).
- Identifying reliable biomarkers for predicting cGvHD and TRM is crucial for improving patient outcomes.
Purpose of the Study:
- To evaluate the predictive value of peripheral blood activated HLA-DR+CD3+ T cells as a novel biomarker for TRM and cGvHD.
- To determine the correlation between specific counts of activated T cells and the incidence of TRM and cGvHD post-HSCT.
Main Methods:
- Retrospective analysis of 107 patients undergoing allogeneic HSCT.
- Measurement of peripheral blood HLA-DR+CD3+ T cells using flow cytometry at 3 months post-HSCT.
- Statistical correlation analysis between T cell counts and clinical outcomes (TRM, cGvHD).
Main Results:
- A peripheral blood HLA-DR+CD3+ T cell count below 140 cells/µL at 3 months post-HSCT was significantly associated with increased TRM.
- Counts below 100 cells/µL correlated with a higher rate of cGvHD (grade 2-3).
- Subgroup analyses confirmed these associations in patients who received reduced intensity conditioning.
Conclusions:
- Low levels of peripheral blood activated HLA-DR+CD3+ T cells at 3 months post-HSCT may serve as a novel predictive biomarker.
- This biomarker can help identify patients at higher risk for TRM and severe cGvHD.
- Early identification allows for potential intervention and improved management strategies in HSCT recipients.
Abstract:
Chronic graft vs host disease (cGvHD) is a major late determinant of transplant related mortality (TRM) after allogeneic hematopoietic stem cell transplantation (HSCT). We investigated the predictive value of peripheral blood activated HLA-DR+CD3+ T cells as a novel biomarker. In total, 107 patients were included in this retrospective analysis. Peripheral blood HLA-DR+CD3+ T cells were measured by flow cytometry 3 mo after HSCT. A HLA-DR+CD3+ T cell count <140 cells/µL at month 3 after HSCT correlated significantly with an increased TRM. A HLA-DR+CD3+ T cell count <100 cells/µL was associated with a higher rate of cGvHD grade 2 to 3. Subgroup analyses revealed significant results for TRM and cGvHD grade 2 to 3 for patients with a reduced intensity conditioning. In summary, low HLA-DR+CD3+ T cells in the peripheral blood 3 mo after HSCT may represent a novel biomarker to identify patients with an increased risk for TRM and cGvHD grade 2 to 3.
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