Seven children with short bowel syndrome underwent small bowel allogra
fting. Episodes of early rejection were observed in five patients who
received a graft from paediatric or adult donors but not in two patien
ts who received a neonatal graft. This study aimed, firstly, to define
immunohistochemical parameters accompanying rejection and, secondly,
to compare immunohistochemical parameters in neonatal grafts with thos
e in grafts from older donors. An immunohistochemical analysis was per
formed on 85 intestinal biopsy specimens taken for monitoring the tran
splants. Acute histological rejection was associated with pericryptic
infiltrates of CD3+-TcR alpha beta+T cells containing clusters of CD8 cells, numerous CD25+ cells, and increased numbers of CD68+ macrophag
es. These changes were associated with the appearance of major histoco
mpatibility (MHC) class II antigens on crypt enterocytes and with an a
ppreciable increase in the expression of E-selectin on mucosal endothe
lial cells. Immunohistochemistry was useful in predicting rejection by
showing the appearance of pericryptic CD25+ T cells 48 hours before t
he first histological lesions of crypt necrosis. Comparison of neonata
l grafts with grafts from older donors did not show any significant di
fference in the density of CD68+ macrophages or in the endothelial exp
ression of intercellular adhesion molecule-1, vascular cell adhesion m
olecule-1, or E-selectin. In contrast to grafts from older donors, how
ever, neonatal grafts did not express MHC class II antigens on epithel
ial cells and contained very low numbers of intraepithelial lymphocyte
s. These data indicate, firstly, that immunohistochemistry is useful f
or monitoring intestinal transplants and, secondly, that the better cl
inical tolerance of neonatal allografts may be related to the lower im
munogenicity of the neonatal epithelium.