PMID- 16646673 OWN - NLM STAT- MEDLINE DCOM- 20060710 LR - 20171116 IS - 1547-3287 (Print) IS - 1547-3287 (Linking) VI - 15 IP - 2 DP - 2006 Apr TI - No polarization of type 1 or type 2 precursor dendritic cells in peripheral blood stem cell collections of non-hodgkin's lymphoma patients mobilized with cyclophosphamide plus G-CSF, GM-CSF, or GM-CSF followed by G-CSF. PG - 269-77 AB - Dendritic cells (DCs) are the most efficient antigen-presenting cells and play a role in immune reconstitution after autologous transplantation. Recent reports suggest that mobilization with granulocyte colony-stimulating factor (G-CSF) containing regimens polarizes DCs into pDC2, which could potentially result with increased Th2 response and decreased graft-versus-host disease (GVHD) in allogeneic transplantation and with decreased cytotoxic Th1 response and graft versus tumor effect, which in autologous transplantation could translate into increased relapse rate. Previously, we have shown that non-Hodgkin's lymphoma (NHL) patients receiving cyclophosphamide (CTX) plus granulocyte- macrophage (GM)-CSF, G-CSF or GM-CSF followed by G-CSF for stem cell collection, mobilize up to five-fold more mature CD80(+) DCs compared to CTX plus G-CSF mobilized patients. Here, we analyzed samples from the same study for the number of pDC1 and pDC2 subsets in blood and apheresis products obtained from these patients. Samples from 29 patients were collected. Patients mobilized with CTX plus G-CSF collected a mean of 1.2 +/- 0.4 x 10(6) pDC1/kg per day and 2.2 +/- 1 x 10(6) pDC2/kg per day, whereas patients mobilized with CTX plus GM-CSF collected a mean of 1.1 +/- 0.5 x 10(6) pDC1 and 1.5 +/- 0.9 x 10(6) pDC2/kg per day. Patients mobilized with CTX plus GM-CSF followed by G-CSF collected 2.5 +/- 1.1 x 10(6) pDC1 and 2 +/- 0.5 x 106 pDC2/kg per day, with significantly higher levels of pDC1 +/- pDC2 cells. No significant difference was observed in pDC1/pDC2 ratio between the three mobilization arms. Patients mobilized with the GM-CSFcontaining regimen had a higher probability for survival compared to patients receiving G-CSF alone (median of 55 months vs. 15 months; p = 0.02). These results support the hypothesis that higher levels of DCs in the graft might be associated with prolonged survival of autotransplanted NHL patients. Further similar studies are merited in a larger population of NHL patients. FAU - Gazitt, Yair AU - Gazitt Y AD - University of Texas Health Science Center, San Antonio, 78284, USA. gazitt@uthscsa.edu FAU - Akay, Cagla AU - Akay C FAU - Thomas, Charles 3rd AU - Thomas C 3rd LA - eng PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - United States TA - Stem Cells Dev JT - Stem cells and development JID - 101197107 RN - 0 (Antigens, CD34) RN - 0 (CD11c Antigen) RN - 0 (HLA-DR Antigens) RN - 0 (IL3RA protein, human) RN - 0 (Interleukin-3 Receptor alpha Subunit) RN - 0 (Receptors, Interleukin-3) RN - 143011-72-7 (Granulocyte Colony-Stimulating Factor) RN - 83869-56-1 (Granulocyte-Macrophage Colony-Stimulating Factor) RN - 8N3DW7272P (Cyclophosphamide) SB - IM MH - Adult MH - Aged MH - Antigens, CD34/analysis MH - Blood Component Removal MH - Bone Marrow/drug effects MH - CD11c Antigen/analysis MH - Cyclophosphamide/*pharmacology MH - Dendritic Cells/chemistry/*cytology MH - Female MH - Granulocyte Colony-Stimulating Factor/administration & dosage/*pharmacology MH - Granulocyte-Macrophage Colony-Stimulating Factor/administration & dosage/*pharmacology MH - HLA-DR Antigens/analysis MH - Hematopoietic Stem Cell Mobilization/*methods MH - Hematopoietic Stem Cell Transplantation/methods MH - Humans MH - Interleukin-3 Receptor alpha Subunit MH - Leukocytes/chemistry/cytology MH - Lymphoma, Non-Hodgkin/*therapy MH - Male MH - Middle Aged MH - Receptors, Interleukin-3/analysis MH - Survival Analysis MH - Transplantation, Autologous EDAT- 2006/05/02 09:00 MHDA- 2006/07/13 09:00 CRDT- 2006/05/02 09:00 PHST- 2006/05/02 09:00 [pubmed] PHST- 2006/07/13 09:00 [medline] PHST- 2006/05/02 09:00 [entrez] AID - 10.1089/scd.2006.15.269 [doi] PST - ppublish SO - Stem Cells Dev. 2006 Apr;15(2):269-77. doi: 10.1089/scd.2006.15.269.