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Blood, 1 June 2004, Vol. 103, No. 11, pp. 4330-4335.
Prepublished online as a Blood First Edition Paper on February 12, 2004; DOI 10.1182/blood-2003-09-3325.

Submitted September 29, 2003
Accepted January 30, 2004
Low dendritic cell count after allogeneic hematopoietic stem cell transplantation predicts relapse, death, and acute graft-versus-host disease
Vijay Reddy*, Jose A Iturraspe, Alessandra C Tzolas, Herwig-Ulf Meier-Kriesche, Jesse Schold, and John R Wingard
College of Medicine, University of Florida, Gainesville, FL, USA
Flow Cytometry, Lifesouth Community Blood Centers, Gainesville, FL, USA
* Corresponding author; email: reddyvs{at}medicine.ufl.edu.
Dendritic cells (DC) are key antigen presenting cells, with a potential role in tumor vaccines. We investigated the hypothesis that early reconstitution of DC after allogeneic hematopoietic stem cell transplantation (SCT) improves survival. We also correlated DC reconstitution with complications of relapse and acute graft-versus-host disease (AGVHD). Fifty patients were transplanted between February 2000 and March 2003 with a median follow up of 501 days (range 136-1263). Most received blood stem cells (92%), and the remainder, bone marrow from HLA matched sibling donors for predominantly high risk hematologic malignancies. Around the time of engraftment, peripheral blood was analyzed by flow cytometry for DC, and further divided as DC1 and DC2. Patients with lower DC count (<4.97 cells/mm3) had a significantly worse survival by Kaplan-Meier analysis (p=0.002), increased incidence of relapse (p=0.002), a higher incidence of AGVHD onset (p=0.0005) and a composite end point of relapse or death (p=0.0017). A Cox-proportional Hazard multivariate model adjusted for important covariates confirmed that low DC count is independently associated with death (HR 3.8; p=0.02), time to relapse (HR 11.6; p=0.001) and AGVHD (HR=3.3; p=0.04). The sensitivity and specificity of low DC count in predicting death or relapse is 73% and 75% respectively. Low number of circulating DC significantly increases risk for relapse and acute GVHD and predicts death after allogeneic SCT.

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