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.

PubMed

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.