Defining hepatocellular chimerism in a liver failure patient bridged with hepatocyte infusion

Background. A practical method of monitoring engraftment by transplanted he patocytes for the purpose of bridging human liver failure to native regener ation is described. Methods. A previously healthy 37-year-old female with a a-week history of a febrile illness presented with fulminant liver failure. Findings on admiss ion included the following: illicit drug use, serum hepatitis B surface ant igen positive, grade 1 encephalopathy, prothrombin time (pt) >100 sec, F-7< 1%, NH3 150 mu mol/L, alanine aminotransferase 4079 U/L, total bilirubin le vel 11.4 mg/dl, and glucose 70 mg/dl (on TV D-10). With immunosuppression, 8.8x10(8), 96% viable human hepatocytes were intraportally infused. Clinica l chemistries, total sHLA class I, and ELISA to measure donor-specific sHLA -A(1) and -B-8 were recorded. Serial transjugular liver biopsies were perfo rmed and pooled for histological examination, DNA extraction, and HLA DNA t yping. Results. The patient fully recovered. At months 3 and 4 with donor biopsy s pecimen class I HLA DNA no longer detectable, immunosuppression was tapered off. The patient is clinically normal, serum hepatitis B surface antigen n egative at 10 months of follow-up. Conclusions. Bridging liver failure with donor hepatocytes with HLA class I antigen disparate from recipients is clinically feasible, and allows for a marker, combined with serial graft histology, to safely wean immunosuppres sion when native liver regeneration succeeds.