Upon allogeneic transplantation (Tx) of pancreatic islets under the kidney
capsule of diabetic rats, cells from draining lymph nodes and, to a minor d
egree, bone marrow transiently upregulate CD44 splice variants as detected
by RT-PCR using CD44 variant exon specific primers. Maximal expression was
on day 5 post Tx in lymph nodes and thus precedes islet rejection sufficien
tly (in this model by 5 days) to still permit establishing rescue by immuno
suppressive therapy. CD44 variant exon sequence could therefore serve as ea
rly markers of allograft rejection.