In this issue of the journal, Dr. Luo and co-workers have identified intra-graft hepatitis B virus (HBV) specific lymphocytes in HBV immune liver donors, (most of whom were live donors) and correlated their findings with the liver transplant recipients' humoral immune responses to HBsAg. 1 HBV specific T and B cells were identified in 59% and 28% of liver grafts respectively in 32 donors. After liver transplantation, almost half of the transplanted patients with chronic HBV developed anti-HBs seroconversion which correlated with the number of donor graft derived HBsAg specific T cells. The investigators suggest that these donor derived HBV specific lymphocyte may be the vehicle through which adoptive transfer of immunity is transferred from HBV immune donors to liver graft recipients with persistent HBV infection. This important study provides for the first time evidence on HBV specificity of intrahepatic lymphocytes isolated from human liver grafts and transplanted to patients with chronic HBV infection. The study sheds further light on the presumed mechanism involved in adoptive transfer of immunity in the setting of parenchymatous organ transplantation. Furthermore, it may take us one step forward in the quest for developing new means for the so called "vaccinotherapy" for controlling persistent HBV infection.Analysis of the reported data requires a short look back on the progress already achieved in this exciting area of clinical research.Patients with acute HBV infection who recover spontaneously are able to clear HBV from the circulation by mounting an effective innate, cellular and humoral immune response leading to long-term, usually life-long immunity. 2,3 Some patients may clear the virus from the circulation, but remain with occult HBV infection with covalently closed circular (ccc) HBV-DNA "hiding" in hepatocytes. Yet, these recovered patients rarely reactivate HBV infection in the presence of an intact immune system and "immune memory" which serve as a gate keeper for prevention or suppression of viral replication and its consequences. In contrast, patients with persistent HBV infection are often tolerant to HBV and unable to mount an effective cellular and humoral immune response toward nucleocapsid and envelope proteins of the virus. This is also true for HBV patients undergoing liver transplantation who in addition to this immunologic defect are also immune suppressed by pharmacologic agents for prevention of graft rejection.Current strategies for protection of HBV liver transplant recipients at risk include lifelong monotherapy with hepatitis B immune globulin (HBIG) or a nucleoside analogue or combination therapy using the two agents simultaneously and indefinitely or at least for a defined period, followed by life-long monotherapy. 4 These strategies, which also include pre-transplant suppression of HBV viral load, have led to an impressive success rate in prevention of HBV graft re-infection in about 90% of patients treated with combination therapy. However, although the risk of graft re-infec...