TY - JOUR
T1 - Histopathologic and molecular evaluation of the Organ Procurement and Transplantation Network selection criteria for intestinal graft donation
AU - Roskott, Anne Margot C.
AU - van Haaften, Wouter T.
AU - Leuvenink, Henri G. D.
AU - Ploeg, Rutger J.
AU - van Goor, Harry
AU - Blokzijl, Tjasso
AU - Ottens, Petra J.
AU - Dijkstra, Gerard
AU - Nieuwenhuijs, Vincent B.
N1 - Copyright © 2014 Elsevier Inc. All rights reserved.
PY - 2014/6
Y1 - 2014/6
N2 - BACKGROUND: The Organ Procurement and Transplantation Network (OPTN) has formulated criteria for the selection of donors for intestinal transplantation. To date, however, no study has correlated histologic findings of intestinal injury with the OPTN criteria. We aimed to describe histopathologic and molecular features of allograft injury in relation to donor conditions defined by the OPTN criteria.MATERIALS AND METHODS: Graft histology (Park Score), Claudin-3 staining, systemic inflammatory markers (C-reactive protein/lipopolysaccharide-binding protein) and expression of heat shock protein 70, heme oxygenase 1, and interleukin 6 were evaluated in multiorgan deceased donors (donation after brain death [DBD] and donation after cardiac death [DCD]).RESULTS: Ninety-seven samples (52 jejunum/45 ileum) were recovered from 59 donors (46 DBD/13 DCD). The OPTN criterion cold ischemia time correlated with histologic injury (Park score) to which the jejunum appeared more susceptible than the ileum. Claudin-3 staining was higher, and heat shock protein 70 expression lower in donors meeting the OPTN criteria compared with donors not meeting the criteria and in DBD versus DCD. In DBD donors, interleukin 6 expression was higher compared with DCD donors and inversely related to C-reactive protein.CONCLUSIONS: Our multiparameter analysis suggests that the OPTN criteria can be discriminative concerning intestinal graft quality. Our data suggest that DCD intestinal allografts are qualitatively inferior and that the jejunum is more sensitive to ischemia than the ileum.
AB - BACKGROUND: The Organ Procurement and Transplantation Network (OPTN) has formulated criteria for the selection of donors for intestinal transplantation. To date, however, no study has correlated histologic findings of intestinal injury with the OPTN criteria. We aimed to describe histopathologic and molecular features of allograft injury in relation to donor conditions defined by the OPTN criteria.MATERIALS AND METHODS: Graft histology (Park Score), Claudin-3 staining, systemic inflammatory markers (C-reactive protein/lipopolysaccharide-binding protein) and expression of heat shock protein 70, heme oxygenase 1, and interleukin 6 were evaluated in multiorgan deceased donors (donation after brain death [DBD] and donation after cardiac death [DCD]).RESULTS: Ninety-seven samples (52 jejunum/45 ileum) were recovered from 59 donors (46 DBD/13 DCD). The OPTN criterion cold ischemia time correlated with histologic injury (Park score) to which the jejunum appeared more susceptible than the ileum. Claudin-3 staining was higher, and heat shock protein 70 expression lower in donors meeting the OPTN criteria compared with donors not meeting the criteria and in DBD versus DCD. In DBD donors, interleukin 6 expression was higher compared with DCD donors and inversely related to C-reactive protein.CONCLUSIONS: Our multiparameter analysis suggests that the OPTN criteria can be discriminative concerning intestinal graft quality. Our data suggest that DCD intestinal allografts are qualitatively inferior and that the jejunum is more sensitive to ischemia than the ileum.
KW - Graft donation criteria
KW - Donor quality
KW - Intestinal graft
KW - Intestinal graft donation
KW - Intestinal transplantation
KW - Organ viability
KW - SMALL-BOWEL TRANSPLANTATION
KW - LIVING-DONOR LIVERS
KW - BRAIN-DEATH
KW - ISCHEMIA-REPERFUSION
KW - LUMINAL PRESERVATION
KW - INFLAMMATORY MARKERS
KW - UNITED-STATES
KW - ILEAL GRAFTS
KW - INJURY
KW - RAT
U2 - 10.1016/j.jss.2014.02.008
DO - 10.1016/j.jss.2014.02.008
M3 - Article
C2 - 24655665
SN - 0022-4804
VL - 189
SP - 143
EP - 151
JO - Journal of Surgical Research
JF - Journal of Surgical Research
IS - 1
ER -