Biology of Blood and Marrow Transplantation
Volume 16, Issue 7 , Pages 985-993 , July 2010

Endothelial Dysfunction after Hematopoietic Stem Cell Transplantation: Role of the Conditioning Regimen and the Type of Transplantation

  • Marta Palomo

      Affiliations

    • Hemotherapy-Hemostasis Department, Centre de Diagnòstic Biomèdic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Hospital Clínic, Universitat de Barcelona, Barcelona, Spain
    • Corresponding Author InformationCorrespondence and reprint requests: Marta Palomo, Pre-doctoral Hemotherapy-Hemostasis Department, Hospital Clinic, Villarroel 170, 08036 Barcelona, Spain.
  • ,
  • Maribel Diaz-Ricart

      Affiliations

    • Hemotherapy-Hemostasis Department, Centre de Diagnòstic Biomèdic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Hospital Clínic, Universitat de Barcelona, Barcelona, Spain
  • ,
  • Carla Carbo

      Affiliations

    • Immune Disease Institute, Department of Pathology, Harvard Medical School, Boston, Massachusetts
  • ,
  • Montserrat Rovira

      Affiliations

    • Stem Cell Transplantation Unit, Hematology Department, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Hospital Clínic, Universitat de Barcelona, Barcelona, Spain
  • ,
  • Francesc Fernandez-Aviles

      Affiliations

    • Stem Cell Transplantation Unit, Hematology Department, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Hospital Clínic, Universitat de Barcelona, Barcelona, Spain
  • ,
  • Carmen Martine

      Affiliations

    • Stem Cell Transplantation Unit, Hematology Department, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Hospital Clínic, Universitat de Barcelona, Barcelona, Spain
  • ,
  • Gabriela Ghita

      Affiliations

    • Stem Cell Transplantation Unit, Hematology Department, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Hospital Clínic, Universitat de Barcelona, Barcelona, Spain
  • ,
  • Ginés Escolar

      Affiliations

    • Hemotherapy-Hemostasis Department, Centre de Diagnòstic Biomèdic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Hospital Clínic, Universitat de Barcelona, Barcelona, Spain
  • ,
  • Enric Carreras

      Affiliations

    • Stem Cell Transplantation Unit, Hematology Department, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Hospital Clínic, Universitat de Barcelona, Barcelona, Spain

Received 8 October 2009 ,Accepted 4 February 2010.

  • Image Result

    Changes in plasmatic levels of vWF and ADAMTS-13 activity. Graphs represent changes in VWF (●) and ADAMTS-13 activity (○) levels in plasma samples from recipients of autologous HSCT with BEAM and MLF

    Changes in plasmatic levels of vWF and ADAMTS-13 activity. Graphs represent changes in VWF (●) and ADAMTS-13 activity (○) levels in plasma samples from recipients of autologous HSCT with BEAM and MLF conditioning treatments, and of allogeneic HSCT with Cy/TBI and Flu/MLF treatments, as indicated. Levels were determined at the different time points of the study: before starting conditioning regimen (Pre), immediately before the infusion of the hematopoietic stem cells (day 0), and days 7, 14, and 21 after the HSCT. Data are expressed as ratios with respect to the Pre value and correspond to mean ± SEM (∗P < .05; n = 6, 5, 5, and 8 for the BEAM, MLF, Cy/TBI, and Flu/MLF, respectively).

  • Image Result
    Changes in the levels of sVCAM-1 and sICAM-1 in patients without TRC from the autologous and allogeneic groups. Graphs represent changes in soluble VCAM-1 and ICAM-1 levels in plasma from recipients o

    Changes in the levels of sVCAM-1 and sICAM-1 in patients without TRC from the autologous and allogeneic groups. Graphs represent changes in soluble VCAM-1 and ICAM-1 levels in plasma from recipients of autologous HSCT with BEAM (●) and MLF (○) conditioning treatments, and of allogeneic HSCT with Cy/TBI (▴) and Flu/MLF (Δ) treatments. Levels were determined at the different time points of the study: before starting conditioning regimen (Pre), immediately before the infusion of the hematopoietic stem cells (day 0), and days 7, 14, and 21 after the HSCT. Data are expressed as ratios with respect to the Pre value and correspond to mean ± SEM (∗P < 0.05; n = 6, 5, 5, and 8 for the BEAM, MLF, Cy/TBI, and Flu/MLF, respectively).

  • Image Result
    Levels of plasmatic soluble TNF receptor I in patients without TRC. Graphs representing changes in soluble TNFRI levels in plasma from recipients of autologous HSCT with BEAM (●) and MLF (○) condition

    Levels of plasmatic soluble TNF receptor I in patients without TRC. Graphs representing changes in soluble TNFRI levels in plasma from recipients of autologous HSCT with BEAM (●) and MLF (○) conditioning treatments, and of allogeneic HSCT with Cy/TBI (▴) and Flu/MLF (▵) treatments. Levels were determined at the different time points of the study: before starting conditioning regimen (Pre), immediately before the infusion of the hematopoietic stem cells (day 0), and days 7, 14, and 21 after the HSCT. Data are expressed as ratios with respect to the Pre value and correspond to mean ± SEM (∗P < .05; n = 6, 5, 5, and 8 for the BEAM, MLF, Cy/TBI and Flu/MLF, respectively).

  • Image Result
    Kinetics of VWF in patients with TRC versus those without complications. Graphs show VWF levels in recipients of autologous HSCT (a) and allogeneic HSCT (b and c) with (•) and without (o) transplant r

    Kinetics of VWF in patients with TRC versus those without complications. Graphs show VWF levels in recipients of autologous HSCT (a) and allogeneic HSCT (b and c) with () and without (o) transplant related complications. ES = engraftment syndrome (n =11); GVHD = graft-versus-host disease (n = 7); VOD = venooclusive disease (n = 2). Data are expressed as absolute values in % (mean ± SEM) (∗P < .05; for days 7, 14, and 21 versus day Pre).

 Financial disclosure: See Acknowledgments on page 992.

PII: S1083-8791(10)00064-9

doi: 10.1016/j.bbmt.2010.02.008

Biology of Blood and Marrow Transplantation
Volume 16, Issue 7 , Pages 985-993 , July 2010