T. Kiuchi et al., BACKGROUND AND PROGNOSTIC IMPLICATIONS OF PERIREPERFUSION TISSUE-INJURIES IN HUMAN LIVER-TRANSPLANTS - A PANEL HISTOCHEMICAL-STUDY, Transplantation, 66(6), 1998, pp. 737-747
Background. Hepatic graft reperfusion is associated with inflammatory
processes of unknown relevance to the fate of graft. This study aimed
to clarify this relevance by histochemical analyses of human hepatic g
rafts. Methods. Paired tissue samples were taken at the end of cold pr
eservation and 2 hr after reperfusion (n=39). From six additional graf
ts, biopsies were performed at the end of cold preservation only. Inju
ry or inflammatory markers of sinusoidal endothelium (von Willebrand f
actor-related antigen [vWF]), Kupffer cells (25F9), platelets (CD62),
neutrophil leukocytes (CD11b), interleukin (IL)-1 beta, intercellular
adhesion molecule (ICAM)-1, and HLA-DR were evaluated semiquantitative
ly by indirect immunoperoxidase staining. Steatosis was also evaluated
by hematoxylin and eosin staining. Results. vWF, CD62(+) platelet agg
regation, CD11b(+) leukocytes, and IL-1 beta levels increased after re
perfusion, and these levels correlated with prereperfusion levels. Not
only vWF, CD62(+) platelets, CD11b(+) leukocytes, IL-1 beta, ICAM-1,
and steatosis after reperfusion, but also IL-1 beta, ICAM-1, and steat
osis before reperfusion correlated with postoperative peak transaminas
e. Furthermore, vWF, CD11b(+) leukocytes, 25F9(+) macrophages, and ICA
M-1 after reperfusion were associated with primary graft nonfunction a
nd strong expressions of ICAM-1 or HLA-DR with early acute rejection.
Although some markers (IL-1 beta, CD62(+) platelets, and CD11b(+) leuk
ocytes) correlated with preharvesting parameters (donor age or length
of intensive care unit stay), none showed any significant correlation
with cold preservation. Conclusion. Synergistic inflammatory events in
the hepatic graft at reperfusion, which have a significant impact on
the later clinical course, are largely defined and precipitated by inj
ury or activation of nonparenchymal cells preceding reperfusion or eve
n graft harvesting.