TY - JOUR
T1 - Enumeration of bone marrow plasmacytoid dendritic cells by multiparameter flow cytometry as a prognostic marker following allogeneic hematopoietic stem cell transplantation
AU - Su, Ruijun Jeanna
AU - Green, Ralph
AU - Chen, Mingyi
N1 - Funding Information:
The study was partially supported by Collaborative Institutional Research Pilot Grant for Investigators in Oncology, the Cancer Research Coordinating Committee (CRCC) and academic senate grants from University of California (MC). We thank Dr. Mehrdad Abedi and Mr. Mark Junyang Jiang for their assistance in patient information collection.
Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2018/3
Y1 - 2018/3
N2 - Plasmacytoid dendritic cells (pDCs) promote tolerance in solid organ transplants and hematopoietic stem cell transplantation (HSCT). pDCs originate from CD34 + hematopoietic progenitors. Following allogeneic hematopoietic stem cell transplant (allo-HSCT), pDC reconstitution in the BM and PB gradually attain levels similar to those in healthy individuals. We have investigated the recovery of pDC following allo-HSCT as a means to predict successful marrow engraftment. We retrospectively studied immune reconstitution of pDC in the BM of 48 patients following allo-HSCT for initial diagnoses of leukemia or other malignancies. Multi-parameter flow cytometry was used to detect the CD45 + CD123 bright HLA-DR + CD4 low pDCs in BM aspirates at 2–14 months (median 6 months) post allo-HSCT. Percentages of pDCs were analyzed along with engraftment, acute graft-versus-host disease (aGVHD), event-free survival, relapse and death over a period of up to 39 months (median 30) following HSCT. We report that higher levels of pDCs in the BM post-HSCT are associated with successful engraftment, less severity of aGVHD, lower relapse rate, higher event-free survival and overall survival (P value < 0.05 for all). pDC levels detected at a shorter time interval 2–8 months (median 5 months) following HSCT also showed similar results. We conclude that pDC numbers are associated with HSCT engraftment and overall survival. Flow cytometry offers rapid quantification of pDCs as an early predictor of outcome following HSCT.
AB - Plasmacytoid dendritic cells (pDCs) promote tolerance in solid organ transplants and hematopoietic stem cell transplantation (HSCT). pDCs originate from CD34 + hematopoietic progenitors. Following allogeneic hematopoietic stem cell transplant (allo-HSCT), pDC reconstitution in the BM and PB gradually attain levels similar to those in healthy individuals. We have investigated the recovery of pDC following allo-HSCT as a means to predict successful marrow engraftment. We retrospectively studied immune reconstitution of pDC in the BM of 48 patients following allo-HSCT for initial diagnoses of leukemia or other malignancies. Multi-parameter flow cytometry was used to detect the CD45 + CD123 bright HLA-DR + CD4 low pDCs in BM aspirates at 2–14 months (median 6 months) post allo-HSCT. Percentages of pDCs were analyzed along with engraftment, acute graft-versus-host disease (aGVHD), event-free survival, relapse and death over a period of up to 39 months (median 30) following HSCT. We report that higher levels of pDCs in the BM post-HSCT are associated with successful engraftment, less severity of aGVHD, lower relapse rate, higher event-free survival and overall survival (P value < 0.05 for all). pDC levels detected at a shorter time interval 2–8 months (median 5 months) following HSCT also showed similar results. We conclude that pDC numbers are associated with HSCT engraftment and overall survival. Flow cytometry offers rapid quantification of pDCs as an early predictor of outcome following HSCT.
KW - Allogeneic hematopoietic stem cell transplantation
KW - Flow cytometry
KW - Outcome
KW - Plasmacytoid dendritic cells
KW - Prognosis
UR - http://www.scopus.com/inward/record.url?scp=85033608624&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85033608624&partnerID=8YFLogxK
U2 - 10.1016/j.bcmd.2017.10.004
DO - 10.1016/j.bcmd.2017.10.004
M3 - Article
C2 - 29137845
AN - SCOPUS:85033608624
SN - 1079-9796
VL - 69
SP - 107
EP - 112
JO - Blood Cells, Molecules, and Diseases
JF - Blood Cells, Molecules, and Diseases
ER -