Virology 1990; 177: 406. 28. Levrero M, Balsano C, Natoli G, Avantaggiati ML. Hepatitis B virus X protein transactivates the long terminal repeats of hu- man immunodeficiency virus types 1 and 2. J Virol 1990; 64: 3082. 29. Laure F, Chatenoud L, Pasquinelli C, Gazengel C, Beaurain G, Torchet MF, et al. Frequent lymphocytes infection by hepatitis B virus in haemophiliacs. Br J Haematol 1987; 65: 181. 30. Kimberlin DW, Whitley RJ. Human herpesvirus-6: neurologic implications of a newly-described viral pathogen. J Neurol Virol 1998; 4: 474. 31. Wang F-Z, Linde A, Hagglund H, Testa M, Locasciulli A, Ljung- man P. Human herpesvirus 6 DNA in cerebrospinal fluid spec- imens from allogeneic bone marrow transplant patients: does it have clinical significance? Clin Infect Dis 1999; 28: 562. 32. Paterson DL, Singh N, Gayowski T, Carrigan DR, Marino IR. Encephalopathy associated with human herpesvirus 6 in a liver transplant recipient. Liver Transpl Surg 1999; 5: 454. 33. Mookerjee BF, Vogelsang G. Human herpes virus-6 encephalitis after bone marrow transplantation: successful treatment with ganciclovir. Bone Marrow Transplant 1997; 20: 905. 34. Cole PE, Stiles J, Boulad R, Small TN, O’Reilly J, George D, et al. Successful treatment of human herpesvirus 6 encephalitis in a bone marrow transplant recipient. Clin Infect Dis 1998; 27: 653. 35. Dockrell DH, Mendez JC, Jones M, Harmsen WS, Ilstrup DM, Smith TF, et al. Human herpesvirus 6 seronegativity before transplantation predicts the occurrence of fungal infection in liver transplant recipients. Transplantation 1999; 67: 399. 36. Flamand L, Gosselin J, Stefanescu I, Ablashi D, Menezes J. Im- munosuppressive effect of human herpesvirus 6 on T-cell func- tions: suppression of interleukin-2 synthesis and cell prolifer- ation. Blood 1995; 85: 1263. 37. Burd EM, Carrigan DR. Human herpesvirus 6 (HHV-6) associ- ated dysfunction of blood monocytes. Virus Res 1993; 29: 79. 38. Roberts JP, Ascher NL, Lake J, Capper J, Purohit S, Garovoy M, et al. Graft versus host disease after liver transplantation in humans: a report of four cases. Hepatology 1991; 14: 274. 39. DePaoli AM, Bitran J. Graft versus host disease and liver trans- plantation. Ann Intern Med 1992; 117: 170. 40. Collins RH, Cooper B, Nikaein, Klintmalm GB, Fay JW. Graft- versus-host disease in a liver transplant recipient. Ann Intern Med 1992; 116: 391. 41. Appleton AL, Sviland L, Peiris JSM, Taylor CE, Wilkes J, Green MA, et al. Human herpes virus-6 infection in marrow graft recipients: role in pathogenesis of graft-versus-host disease. Newcastle Upon Tyne Bone Marrow Transport Group. Bone Marrow Transplant 1995; 16: 777. 42. Wilborn F, Brinkman V, Schmidt CA, Neipel F, Gelderblom H, Siegert W. Herpesvirus type 6 in patients undergoing bone marrow transplantation: serologic features and detection by polymerase chain reaction. Blood 1994; 83: 3052. 43. Brown, NA, Sumaya, C V, Liu, C R, et. al. Fall in human herpes- virus-6 seropositivity with age[Letter]. Lancet 1988; 13: 396. Received 28 September 1999. Accepted 8 March 2000. 0041-1337/00/6912-2573/0 TRANSPLANTATION Vol. 69, 2573–2580, No. 12, June 27, 2000 Copyright © 2000 by Lippincott Williams & Wilkins, Inc. Printed in U.S.A. LONG-TERM RESULTS AFTER CONVERSION FROM CYCLOSPORINE TO TACROLIMUS IN PEDIATRIC LIVER TRANSPLANTATION FOR ACUTE AND CHRONIC REJECTION JORGE REYES, 1 ASHOK JAIN,GEORGE MAZARIEGOS,RANDEEP KASHYAP,MIKE GREEN, KATHY IURLANO, AND JOHN FUNG Thomas E. Starzl Transplantation Institute,University of Pittsburgh Medical Center and Children Hospital, Pittsburgh, PA 15213 Tacrolimus is beneficial in liver transplantation for reversing steroid-resistant acute rejection, and for controlling the process of chronic rejection in allo- graft recipients receiving Cyclosporine- (CyA) based regimens. Very little is known about the long-term efficacy of tacrolimus in pediatric transplantation af- ter conversion from CyA. Our study examines the long- term outcome after conversion to tacrolimus for acute or chronic rejection in pediatric liver transplant (LTx) recipients. Method. Seventy-three children (age < 18 years) re- ceiving their primary LTx under CyA between August 1989 and April 1996 were converted to tacrolimus for ongoing acute rejection (n22, group I) or chronic rejection (n51, group II). Mean age at the time of conversion was 10.25.5 years with a mean interval from LTx to conversion of 3.52.9 (range 0.5–10.1 years). There were 33 boys and 40 girls. All patients were followed until June 1999. Mean follow-up was 97.317.4 months (range 62.4 –118.9 months). Results. Overall 5-year actual patient survival was 78.1% and 8-year actuarial survival was 74.6%. Pa- tients converted to tacrolimus therapy to resolve acute rejection (group I) experience significantly bet- ter patient and graft survival at 5 and 8 years than those converted to resolve chronic rejection (group 1 Address correspondence to: Jorge Reyes, Thomas E. Starzl Transplantation Institute, 3601 Fifth Avenue, 4c Falk Clinic, Pitts- burgh, PA 15213. REYES ET AL. June 27, 2000 2573