Rodent studies of nerve allografts are limited by a relatively short length
of graft segment. The authors attempted to establish an outbred sheep mode
l that would allow the study of longer, more clinically relevant nerve gaps
. Using outbred ewes, two 8-cm long radial sensory nerves were grafted into
gaps (5 cm) in the median nerve. Sheep received an autograft and an allogr
aft. Four sheep were immunosuppressed with Cyclosporin A (CsA) and four wer
e controls. Blood CsA levels greater than 1000 mu g/L were obtained. System
ic immunosuppression resulted in severe opportunistic infections, and the s
heep were sacrificed between 35 and 47 days following surgery. Histological
ly, in the autografts and CsA-treated allografts, evidence of nerve regener
ation was seen. Non-immunosuppressed allografts were clearly rejected. Whil
e clear differences in the histology of experimental and control grafted ne
rve tissues were seen, the sheep allograft model presents considerable chal
lenges due to immunosuppression-related infectious complications.