TY - JOUR
T1 - An engraftment syndrome in autologous stem cell transplantation related to mononuclear cell dose
AU - Edenfield, W. J.
AU - Moores, L. K.
AU - Goodwin, G.
AU - Lee, N.
N1 - Funding Information:
We wish to express gratitude for the support of the ward 71 staff for assistance during this review, and the support from the Department of Clinical Investigation, Walter Reed Army Medical Center.
PY - 2000
Y1 - 2000
N2 - Engraftment syndrome (ES) is a toxicity of autologous stem cell transplantation that occurs unexpectedly and is occasionally fatal. This syndrome, manifested as fever, rash and pulmonary deterioration which becomes evident at marrow engraftment, has been described by several centers but as yet remains enigmatic. We describe this syndrome at a single institution and note that it has accompanied the transition from the use of autologous marrow rescue to peripheral blood stem cell rescue. In this study, the occurrence of ES is related to the mononuclear cell dose at reinfusion. We found, in agreement with other reports, that patients developing ES are predominantly women undergoing therapy for solid tumors who demonstrate neutrophil engraftment at a significantly greater rate than do those patients not expressing the syndrome. We did not note a significant relationship between growth factor use (G-CSF) or amphotericin B exposure and the syndrome, as has been previously reported. The progenitor cell populations obtained with autologous marow and peripheral blood stem cells are different. We hypothesize that the interaction of committed myeloid precursors from the stem cell product with the pulmonary vascular endothelium can be deleterious, especially under the influence of the inflammatory cytokines present at the time of engraftment.
AB - Engraftment syndrome (ES) is a toxicity of autologous stem cell transplantation that occurs unexpectedly and is occasionally fatal. This syndrome, manifested as fever, rash and pulmonary deterioration which becomes evident at marrow engraftment, has been described by several centers but as yet remains enigmatic. We describe this syndrome at a single institution and note that it has accompanied the transition from the use of autologous marrow rescue to peripheral blood stem cell rescue. In this study, the occurrence of ES is related to the mononuclear cell dose at reinfusion. We found, in agreement with other reports, that patients developing ES are predominantly women undergoing therapy for solid tumors who demonstrate neutrophil engraftment at a significantly greater rate than do those patients not expressing the syndrome. We did not note a significant relationship between growth factor use (G-CSF) or amphotericin B exposure and the syndrome, as has been previously reported. The progenitor cell populations obtained with autologous marow and peripheral blood stem cells are different. We hypothesize that the interaction of committed myeloid precursors from the stem cell product with the pulmonary vascular endothelium can be deleterious, especially under the influence of the inflammatory cytokines present at the time of engraftment.
KW - Engraftment syndrome
KW - Mononuclear cell
KW - Peripheral blood stem cells
KW - Progenitor cell
UR - http://www.scopus.com/inward/record.url?scp=0033996952&partnerID=8YFLogxK
U2 - 10.1038/sj.bmt.1702155
DO - 10.1038/sj.bmt.1702155
M3 - Article
C2 - 10723584
AN - SCOPUS:0033996952
SN - 0268-3369
VL - 25
SP - 405
EP - 409
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 4
ER -