A descriptive study of a new model enabling serial biopsies of ongoing
hyperacute rejection of small intestinal discordant xenografts is pre
sented, In a series of guinea-pig-to-Lewis rat small bowel xenotranspl
ants (n=7), aboral free ends of Thierry-Vella loops constructed from t
he graft were sequentially biopsied at one-minute intervals up to ten
minutes post-reperfusion and less frequently thereafter, In a guinea p
ig-to-guinea pig (n=6) isograft series, biopsy controls for preservati
on/ischemia-reperfusion injury were obtained, Xenoantibody sequestrati
on in this model was evaluated in a separate series of transplants, ut
ilizing an ELISA assay for rat anti-guinea pig natural antibodies. Pat
hologic evaluation revealed a unique series of events characterized wi
th microcirculatory failure and thrombosis progressing from the submuc
osal vasculature to the lumen, Within the system's detection limits, c
omplement deposition and P-selectin expression occurred as early as on
e minute post-reperfusion, preceding the staining for IgM and IgG, Usi
ng rat serum ELISAs, no significant difference in xenoantibody sequest
ration was detected between the xenograft and isograft groups, The gui
nea pig-to-rat discordant small bowel xenotransplantation is an effici
ent small animal model to dissect the very early pathophysiologic even
ts during hyperacute rejection.