|Year : 2008 | Volume
| Issue : 1 | Page : 23-50
|Prophylaxis and treatment of Hepatitis B in immunocompromised patients
Alfredo Marzano1, Andrea Marengo1, Pietro Lampertico2
1 Division of Gastroenterology and Hepatology, AOU San Giovanni Battista, Torino, Italy
2 Division of Gastroenterology, Fondazione Policlinico, Mangiagalli Regina Elena, IRCCS Maggiore Hospital, University of Milan, Milano, Italy
Click here for correspondence address and email
|Date of Web Publication||9-Jan-2010|
| Abstract|| |
The literature on hepatitis B virus (HBV) in immunocompromised patients is heterogeneous and refers mainly to the pre-antivirals era. Today a rational approach to the problem of hepatitis B in these patients provides for: a) the evaluation of HBV markers and of liver condition in all subjects starting immunosuppressive therapies (baseline), b) the treatment with antivirals (therapy) of active carriers, c) the pre-emptive use of antivirals (prophylaxis) in inactive carriers, especially if they are undergoing immunosuppressive therapies judged to be at high risk, d) the biochemical and HBsAg monitoring (or universal prophylaxis, in case of high risk immunosuppression) in subjects with markers of previous contact with HBV (HBsAg-negative and antiHBc-positive), in order to prevent reverse seroconversion.
Moreover it is suggested a strict adherence to the criteria of allocation based on the virological characteristics of both recipients and donors in the general setting of transplants, and in liver transplantation the universal prophylaxis with nucleos(t)ides analogues (frequently combined with specific anti-HBV immunoglobulins) in HBsAg-positive candidates and in HBsAg-negative recipients of antiHBc-positive grafts should be adopted.
Keywords: AntiHBc, anti-HBV immunoglobulin, antivirals, chemotherapy, HBsAg, hepatitis B virus (HBV), HBV carrier, immunosuppression, lamivudine, transplantation, prophylaxis.
|How to cite this article:|
Marzano A, Marengo A, Lampertico P. Prophylaxis and treatment of Hepatitis B in immunocompromised patients. Hep B Annual 2008;5:23-50
| Introduction|| |
Hepatitis B virus infection is a major public and medical concern. Two billion people are overt carriers of HBV worldwide; of them, 360 million suffer from chronic HBV infection and over 520,000 die each year, 50,000 from acute hepatitis B and 470,000 from cirrhosis or liver cancer. Moreover many subjects have only markers of previous contact with the HBV (antiHBc+/- antiHBs), which can indicate an occult HBV infection (OBI).
Immunodepression due to the underlying disease or to drugs used in immunosuppressive, anticancer therapy and in organ transplants can influence the hepatitis B virus (HBV), both in terms of reactivation and in terms of the acceleration of a pre-existing chronic hepatitis.
In this situation the possibility of HBV relapse has been known for years, with clinical manifestations ranging from self-limiting anicteric to fulminant forms or to chronic hepatitis with an accelerated clinical course towards liver decompensation. Hepatitis reactivation may influence the continuation of the specific treatments and the survival of immunodepressed or transplanted patients. 
The risk of clinical events is mainly observed in overt carriers of HBV, but can also develop in the OBI condition which has been widely described in the literature of the last decade. 
Progress in the diagnostic procedures of the various virological conditions associated with HBV, the recent availability of effective antiviral treatments, the growing incidence of immunocompromised patients attributable to the evolution of immunosuppressive therapies and organ transplants and the expectation of an important future increase of HBV reactivation have brought this problem to the fore although the rational approach and management of these patients is still debated.
Persistent HBV infection is defined as overt when the hepatitis B surface antigen (HBsAg) is present in amounts well-detectable by sensitive immune assays and occult in HBsAg-negative subjects with evidence of intrahepatic and/or serum HBV DNA.  In occult carriers, HBsAg can be completely absent or undetectable for very low amounts or polymorphisms.
A. HBV carriers (HBsAg-positive). In accordance with the international definitions, they can be identified as: 1) active carriers, in presence of HBeAg or of antiHBe antibodies and of a viral load ≥ 20,000 IU/ml; this condition is associated with the presence of hepatic disease in the most part of cases, or 2) inactive carriers, in case of subjects HBeAg-negative and antiHBe-positive, whose alanine aminotransferase (ALT) levels are persistently within the normal range, HBV DNA below 20,000 IU/ml and IgM antiHBc levels < 0.20 IMx Index. In the majority of these subjects the histological finding, when available, does not reveal a significant liver disease (necroinflammatory activity < 4 HAI), while in a small minority of cases it is possible to observe the effects of a chronic liver disease which became silent spontaneously or following antiviral treatment. ,
B. Occult HBV carriers (HBsAg-negative).The difficulty in determining HBV DNA in the liver biopsy (frequently not justified in subjects without clinical signs of hepatitis), the rare presence of detectable viremia in serum even with sensitive techniques, and the frequent presence in occult carriers of markers of previous contact with the HBV (antiHBc+/- antiHBs), leads to consider all anti-HBc (anti-core)-positive subjects as potential occult carriers. Instead there are no serum determinants in the minority (about 20%) of occult carriers who are negative for all HBV markers.
In HBV carriers (occult or overt) the following virological events are considered significant: 1) in anti-core subjects the re-emergence of HBsAg (reverse-seroconversion), 2) in inactive carriers the appearance of a significant viremia (≥20,000 IU/ml) (reactivation), as this is frequently associated with liver damage due to HBV, 3) in active carriers the persistence of a significant viremia (> 20,000 IU/ml in HBeAg positive patients and > 2,000 IU/ml in HBeAg negative subjects) (activity), as this is frequently associated with progression of liver damage due to HBV, 4) in all the virological categories (whether or not during prophylaxis or therapy with antivirals), the increase in at least one logarithm of HBV DNA, compared to its nadir, reconfirmed in two consecutive serum tests during monitoring (virologic breakthrough) [Table 1]. 
The assessment of chronic liver disease is the fundamental event of the diagnostic picture (baseline) [Table 2] and it requires the use of all the instruments usually utilised in hepatology including, if necessary, trans-cutaneous or trans-jugular liver biopsy in subjects with coagulation problems (for example patients with blood or kidney diseases).
The baseline diagnosis of the disease is pivotal in the choice of which treatment to adopt, as the risk of severe complications is related to the severity of the underlying liver disease. 
In order to standardize the definitions the following terms were suggested: 1) infection (not necessarily associated with reactivation of hepatitis) in the case of the detection of HBV DNA by sensitive HBV assays and/or of HBsAg in patients in whom these markers were originally negative, 2) reactivation of hepatitis B (hepatitis), in the presence of a significant viremia and ALT levels above the upper normal value.
The term prophylaxis was used to mean treatment with antiviral drugs of an inactive or occult infection, with the aim of preventing hepatitis reactivation. Prophylaxis was defined as: 1) universal prophylaxis (UP), if it is carried out on the entire population potentially at risk (inactive carriers and/or anti-core), or targeted prophylaxis (TP), if it is subordinate to the appearance of infection markers (HBV DNA and/or HBsAg) in the absence of hepatitis reactivation [Table 3].
Therapy (T) was understood to mean the treatment of hepatitis B (i.e. chronic hepatitis in active carriers or hepatitis reactivation in previously inactive carriers and in anti-core subjects who develop the reverse seroconversion).
In Italy the following drugs are available at present: interferons, either standard or peghilated (both little tolerated in the condition of immunodepression, especially in transplant patients for the potential risk of rejection) and the nucleos(t)ides analogues (NAs), which include lamivudine, adefovir-dipivoxil and entecavir for those with HBV monoinfection, with the addition of tenofovir and emtricitabine for patients with HBV-HIV co-infection.
Lamivudine, which has a potent antiviral effect, frequently (50-60% at 4 years) induces the selection of lamivudine-resistant mutants in locus YMDD of the polymerase gene (YMDD). Instead adefovir-dipivoxil and entecavir induce a lower selection of mutants in monotherapy (0-3% at 1-2 year and genotypic resistance in 29% at 5 years with adefovir in naοve patients; about 10-20% at 2 years with both drugs in YMDD-carriers). ,,, In carriers of the lamivudine-resistant variant, the combination of adefovir-dipivoxil and lamivudine can synergically control the selection of the respective mutants. 
Data from experience in liver transplanted and HIV patients have shown a relation between the original viremia, the degree of immunosuppression and the selection of mutants during prophylaxis with lamivudine. , Consequently a careful monitoring of the response to treatment and of the resistance is suggested in immunosuppressed patients.
Once NAs therapy or prophylaxis has been started, monitoring will essentially be through testing serum HBV DNA and ALT levels every three months, to assess: 1) response to treatment (i.e. reduction of HBV DNA, preferably below the limit of sensitivity of the amplified techniques and ALT normalization) and 2) drug-resistance, which should be suspected in thecase of virologic breakthrough while on-treatment, in order to activate an early rescue therapy.  Resistance can be defined clinically by the virologic breakthrough  but if available a genotypic testing could be used in order to better define the different mutations and to choose the rescue therapy.
Impact on different specialist fields
Data regarding hepatitis B in immunocompromised patients are very heterogeneous, so the statements reported here below required an extensive review of the literature and the inclusion of expert opinion where information was lacking. As a result there was a strong indication to promote studies aimed at defining the natural history of hepatitis B in these patients, to assess - also prospectively - different treatment protocols, to promote close cooperation among different specialists and, finally, to constantly update the indications.
Of note, in all fields a pre-immunosuppression assessment (baseline) is recommended, in both HBsAg positive and negative subjects.
Oncology, Hematology and Hematopoietic Stem Cell Transplantation (HSCT)
During chemotherapy hepatitis B can make its appearance in two different phases: 1) during the treatment, in relation to the intense bone marrow suppression, which is associated with a strong viral replication and, sometimes, with the emergence of a fulminant hepatitis in the form of fibrosing cholestasis, 2) after the end of therapy, as during the immuno-reconstitution phase the immune response can bring on a reactivation of hepatitis whose clinical course may be more or less severe depending on the baseline condition of the liver and other possible factors that may contribute to the damage.
In oncology the prevalence of HBsAg-positive patients ranges between 5.3% (in Europe) and 12% (in China). In these patients the frequency of clinical HBV reactivation ranges between 20 and 56%, correlating with the use of steroids, anthracyclines, 5-fluouracil with some virological indicators (presence of HBeAg or of e-minus variants and/or of a detectable HBV DNA prior to therapy). The clinical significance of relapse has been clearly associated with the pre-chemotherapy liver function, with a mortality of 5-40%. The reactivation of hepatitis, moreover, influences the continuation of the chemotherapy, inducing its suspension and not infrequently posing problems of differential diagnosis with regard to drug toxicity. Hepatitis B can develop both in active and in inactive carriers and it is generally associated with the reappearance of a significant viremia in the preceding 2-3 weeks.
In hematology the frequency of HBsAg positive patients is higher (12.2% in Greece and 8.8% in a recent study from Italy) and the risk of reactivation appears to be greater than in other settings of oncology, depending on the degree of immunosuppression. In this setting, control of the HBV infection assumes great importance in order to prevent HBV-related complications, but also so as not to modify a highly successful therapeutic schedule. In this field the main prognostic indicators unfavorably associated with hepatitis B reactivation are, besides those already cited, hyper-transaminasemia and the condition of second or third cycle compared to the first.,,,
In hematology, a 21-67% (median 50%) risk of reactivation has been described, with an average mortality of 20%. In this setting, the available literature is not clear whether the severity of hepatitis in HBsAg-positive patients is directly due to the liver damage caused by HBV reactivation or by other causes (i.e. VOD, GvHD or MOF) and also the degree of risk in relation to the condition of active or inactive carrier is not clearly determinable.
The risk would appear to be heightened by the use of monoclonal antibodies (antiCD20, antiCD52), with the possibility of hepatitis reactivation (even after a cycle of 1-3 months of prophylaxis with lamivudine) at a distance of 12-36 months from the last administration of these drugs, particularly in overt carriers, but also in anti-core subjects. An analogous risk exists in the course of allogeneic HSCT, as the immuno-suppressive effect in the conditioning phase is particularly strong and is amplified by the subsequent anti-rejection therapy, so the risk of hepatitis reactivation remains throughout the phase of immuno-reconstitution (in some cases until 1-2 years from transplantation). ,,,,
Experiences in the different virological categories.
1. Active HBsAg-carriers. In the onco-hematological setting lamivudine therapy of chronic hepatitis in active carriers appears to be effective. 
2. Inactive HBsAg-carriers. The start of lamivudine therapy at the time of the clinical relapse (hepatitis) in inactive carriers maintains a residual mortality of 20%, probably in relation to the baseline conditions and to the delayed treatment. However, in retrospective studies lamivudine has been shown to be effective in prophylaxis of hepatitis B (0-9% of hepatitis reactivation compared to 25-85% in untreated patients) and in the only prospective study hepatitis relapse developed in 5% of treated subjects and in 24% of controls. Moreover, in the study the universal use of lamivudine was better than the targeted prophylaxis (activated only at the appearance of HBV DNA with a non-amplified technique, during bimonthly monitoring), both in terms of survival and of hepatitis reactivation (0% vs 53%, P=0.002). ,,,,
Recently two meta-analyses have confirmed the significant efficacy of lamivudine in preventing hepatitis B in HBsAg positive patients (OR 0.09, 95% CI 0.05-0.15 in the first; RR 0.13, 95% CI 0.07-0.24 in the second), in reducing deaths (OR 0.36, 95% CI 0.23-0.56, NNT 11 in the first; RR 0.30, 95% CI 0.1-0.94, NNT 3 in the second) and in reducing chemotherapy discontinuation. Finally, as lately reported in literature, lamivudine-prophylaxis in HBsAg-positive patients undergoing chemotherapy has been shown to be cost-effective in terms of HBV reactivation (9.6% LAM+ vs 43.8% LAM-), liver related deaths (0/500 LAM+ vs 20/500 LAM-), chemotherapy discontinuation and cancer deaths (39/500 LAM+ vs 47/500 LAM-). ,,
3. Anti-core patients (HBsAg-negative). In the oncological setting there are no data, at present, for this virological category, which can reach 20-40% in averagely endemic areas and 70-80% in highly endemic areas. However, in the hematological setting, out of a total of 176 patients described in literature, sero-reversion has been reported in 21 subjects (12%) during conventional chemotherapy, whether or not this was associated with HSCT, with percentages of 4-30% during chemotherapy and 14-50% in the course of autologous transplantation.
After autologous HSCT, hepatitis B developed in anti-core patients later (6-52 months, average 19 months) than in overt carriers (average 2-3 months) and none of the patients described died of hepatitis B (in 7 cases during therapy with lamivudine, started at the time of the clinical relapse). After the reactivation 9 of the 10 patients remained HBsAg positive and one lost the HBsAg during follow-up. Instead, 2 deaths out of 39 subjects with sero-reversion have been reported in literature after allogeneic HSCT and this appeared to have been significantly linked to the absence of protective antibodies (antiHBs) in the donor and to GVHD. 
Recently the introduction in hematologic treatments of monoclonal anti-lymphocyte B and T antibodies (anti-CD20 and antiCD52), used alone or together with chemotherapy, has been associated with the signaling of 6 cases of sero-reversion in anti-core subjects, in 3 cases with a fulminant form and death of the patients, despite therapy with lamivudine. 
HBV infection has been described to be the most frequently (39%) experienced viral infection in lymphoma patients treated with Rituximab. In this study about 50% of Rituximab-related HBV infections resulted in death, whereas this was the case in only 33% of the patients with other infections.
An Italian study has lately stressed a very low (1%) overall risk of sero-reversion in a large series of patients treated for lymphoma, but the risk of hepatitis B reactivation was 3.5 fold increased for Rituximab therapy, compared to conventional chemotherapy (P < 0.005).
Data confirming the increased risk of HBV reactivation in patients undergoing anti B-cell therapy have also emerged in a trial which showed as alemtuzumab containing chemotherapy regimen was associated with a high risk (29%) of reactivation of occult HBV infection and of severe HBV-related hepatitis. ,,
1. In active carriers therapy is considered useful to control the liver disease pre- and post-immunosuppressive treatments. In HSCT, in particular, the control of the HBV-related disease permits a more precise diagnosis and treatment of specific liver complications (GvHD and VOD). In these patients, antiviral therapy should be continued lifelong (due to the high risk of relapse after withdrawal) or at least until the disappearance of HBsAg in serum. A strict monitoring of mutants should be activated, in order to prevent hepatitis relapse with rescue therapy.
2. In the inactive carriers universal prophylaxis appears to be indicated and should be continued for the entire phase of chemotherapy, until at least 6-12 months (also 18 months in patients treated with repeated cycles of monoclonal antibodies) after the end of the treatment.  The optimal duration of the prophylaxis is still debated and requires prospective studies. In any case, the panel recommends monitoring of the viremia after suspension, for the prompt diagnosis and return to treatment in the case of reactivation.
3. In anti-core (HBsAg-negative) patients, two different strategies can be identified:
a) in oncology or in patients undergoing mild hematological therapies (judged to be at low immunosuppressive potential, such as the ABVD of the CHOP 21 days scheme), HBsAg monitoring every 1-3 months is advised, with the activation of targeted prophylaxis or therapy in the case of sero-reversion or hepatitis reactivation, respectively. However, the use of HBV DNA monitoring for targeted prophylaxis remains controversial because of the lack of data referred to the timing and duration of the monitoring and to the clinical significance of minimal levels of detectable viremia (i.e. the presence of low levels of serum HBV DNA in anti-core patients after solid organs transplantation is not constantly associated with hepatitis relapse). 
b) In subjects who need to be treated with intense immunosuppression (chemotherapy with fludarabine, dose-sense regimes, allogeneic transplant, autologous myeloablative transplant, induction in acute leukemia, use of monoclonal antibodies) universal prophylaxis is proposed. This approach is strongly indicated in the hematological setting and in patients with signs of a chronic hepatitis (due to a previous history of HBV-related disease and/or to other causes of chronic hepatitis) and/or with a positive serum HBV DNA and/or positive for antiHBe antibodies at the baseline evaluation. In anti-core subjects clinical studies are recommended in the future.
Effects of different virological conditions in donors (D) and recipients (R) of Allogeneic Hematopoietic Stem Cell Transplantation (HSCT)
1. D (HBsAg-/antiHBs+/antiHBc )->R (HBsAg+). In the case of transplant from an immunized (antiHBs-positive) donor to an overt carrier (HBsAg-positive) recipient two possible scenarios have been described: a) the chance of adoptive transfer of immunity with the possible clearance of HBsAg (especially if recipients are treated with lamivudine), b) an acute and sometimes fulminant hepatitis (in historical series). 
2. D (HBsAg-/antiHBs /anti-core+)->R (HBsAg-/antiHBs /anti-core). Only few data are available, indicating that in the case of transplant from an anti-core donor the risk of sero-reversion in the recipient would appear to be negligible in anti-core positive recipients and greater in the case of complete negativity for the markers of previous contact with HBV (naοve), in analogy with what has been described in the transplant of solid organs. 
3. D (HBsAg+)->R (HBsAg-). In a few studies, transplant from an HBsAg-positive donor was associated with hepatitis in 44-62% of recipients, with generic hepatic mortality in 33-75% of cases, although the role of HBV in these clinical events was not well defined. In a historical retrospective multicenter study performed in the pre-antiviral phase, the anti-HBV specific immunoglobulins (HBIG) were not protective against the transmission of the infection. In contrast, in a recent study the activation of therapy with lamivudine in donors and of prophylaxis with the same antiviral in recipients significantly reduced the HBV-related hepatitis rate (48 vs. 7%, P=0.002) and mortality (24 vs. 0%, P=0.01) compared to a historical control group. 
Furthermore two case-reports have confirmed the efficacy of lamivudine-prophylaxis in this clinical setting in preventing HBV-related hepatitis. ,
General recommendations in HSCT
a. Vaccination of the recipient prior to transplant with accelerated protocols, (recombinant vaccine 40 μg by intramuscular route time 0-1-2 months or 0-7-21 days), especially if he/she is naοve.
b. Vaccination of the donor not immunized prior to transplant, with accelerated protocols (recombinant vaccine 20 ΅g by intramuscular route time 0-1-2 months or 0-7-21 days) in the case of allogeneic HSCT.
c. Preferential allocation of anti-core organs to vaccinated recipients or those with markers of prior contact with HBV.
d. Treatment of the HBsAg-positive donor with lamivudine pre-HSCT in order to reduce infectivity through the reduction of viremia (preferably below the limit of sensitivity of an amplified assay) and universal prophylaxis of the recipient on the day before the transplant.
e. The use of high doses of HBIG (intravenous 10,000 IU) during infusion of hematoopoietic stem cells from overt carriers (who have been preventively treated with antivirals) in HBsAg-negative recipients. There is a lack of data about the neutralizing effect of HBIG in this setting in the antivirals-era, but while awaiting prospective studies there has been recent evidence in the liver transplantation setting of a direct correlation between HBV DNA in serum (now preventively reduced in HBsAg positive recipients by antivirals) and the neutralizing power of the immunoglobulins. 
Because of the actual results of the hepatologic and hematologic therapy there is no reason to deny hematopoietic stem cell transplantation from an HBV positive donor (any form) if the risk-benefit ratio is in favour of transplantation. Moreover in the case of an HLA identical family HBV positive member there is no point in wasting time and resources in searching for an unrelated donor in the international bone marrow donor bank.
Dialysis and solid organs transplants (kidney, heart and lung)
Dialysis. The incidence of overt carriers of HBsAg among dialyzed patients is 0-7% in developed countries and 10-20% in developing ones. In these subjects the frequent normality of the transaminase makes clinical judgment difficult, confirming the fundamental role of the virological markers (quantitative HBV DNA) and of the liver biopsy to distinguish between active and inactive carriers (baseline). In this setting data about the condition of occult carrier among anti-core patients are scarce and consider the sole presence of viremia in serum, whose diagnostic sensitivity is low.
In kidney transplant the condition of HBsAg carrier can be estimated in 10-20% of cases and is associated with a significantly higher risk of death (OR 2.49, 95% CI), independent of the viremic condition (active or inactive carrier), and the chronic hepatitis presents an accelerated course towards cirrhosis (5.3-12%-year), decompensation and hepatocarcinoma. ,
In heart and lung transplant, Italian reports have signalled HBsAg positivity in 2.3-3.7% of recipients. In this setting the evolution of the HBV-related disease is accelerated in active carriers and the risk of hepatitis B reactivation post-transplant is over 50% in originally inactive subjects. Finally, the risk of sero-reversion post-surgery (de-novo hepatitis B) in HBsAg-negative/anti-core recipients seems to be lower than 5%. ,,
Clinical experiences in nephrology
No controlled trials for the treatment of HBV with either interferon or lamivudine in dialyzed patients or in kidney transplants are currently available. Interferon can be used to treat dialyzed patients with chronic hepatitis B, but it is contraindicated in transplanted patients. Short-term administration of lamivudine monotherapy is effective but when the drug is withdrawn, viremia rebounds and hepatitis relapses in most cases. Continuous administration of lamivudine monotherapy for 3 to 4 years is able to obtain long-term suppression of HBV replication and may prevent the development of liver related complications and mortality.  Secondary treatment failure is caused by the emergence of YMDD which, in some patients, herald hepatitic flares and progression of the liver disease.
Recommendations in relation to transplant recipients
1. Active carrier. In candidates for kidney, heart or lung transplant the indication to therapy is confirmed, both in the pre-transplant (with NAs or interferons, when they are tolerated) and in the post-transplant phase (only NAs in view of the high risk of interferon-induced rejection).
2. Inactive carrier. Pre-transplant and during dialysisthere is no indication for prophylaxis but biochemical and virological monitoring is advised, if the diagnosis has been confirmed by strict adherence to previously defined criteria. Instead, therapy should be used in the re-activated forms (HBV DNA >20,000 IU/ml), especially if associated with significant liver damage (HAI > 4 and/or signs of fibrotic disease by non-invasive methods). Post-transplant, however, there is an indication to universal prophylaxis, in relation to the available data on mortality in HBV carriers, independentlyfrom their virological condition. 
3. Anti-core recipient. In HBsAg-negative and anti-corepositive recipients of kidney, heart and lung transplant the presence of subclinical manifestations (low levels of circulating HBV DNA detectable with amplified techniques post-transplant) without sero-reversion in over 95% of cases ,,, has been indicated. In this condition only monitoring of the HBsAg is required, with the activation of targeted prophylaxis or therapy only in the case of sero-reversion and/or hepatitis, respectively.
Recommendations in relation to transplant donors
1. Anti-core donors. In the case of kidney, heart or lung allocation from an HBsAg-negative/anti-core positive/antiHBs-positive or negative donor in a HBsAg-negative recipient, the risk of hepatitis B appears to be less than 5%. , The low risk does not justify preventive prophylaxis, but only HBsAg monitoring (every 3-6 months and/or in the case of transaminase increase) and the use of targeted prophylaxis or therapy only in the case of sero-reversion. In analogy to what has been signaled before the risk connected with the use of anti-core positive organs is further reduced by the indications reported in Section "General recommendations in HSCT".
2. HBsAg-positive donors. In this condition the risk of transmission of the HBV infection is very high in the absence of prophylaxis, especially from HBeAg-positive donors.  Recently a report has indicated the post-transplant control of hepatitis B in HBsAg-negative/antiHBs-positive recipients of kidneys from HBsAg-positive donors (HBeAg and HBV DNA-negative) while on lamivudine prophylaxis.  In Italy the use of these organs is controlled by national guidelines (www.governo.it/GovernoInforma/Dossier/donatori_organi/linee_guida.html).
The risk of post transplantation hepatitis B is strictly influenced from both recipient and donor virological characteristics:
a) HBsAg-positive recipients: in the absence of pre- and post-operative prophylaxis the risk of post-transplantation hepatitis B is over 80%. In this condition the use of antivirals before transplant (one single antiviral in the case of wild type virus, combined with a second one that is active on the mutants, in the condition of drug resistance with active replication), associated with HBIG after surgery (combined prophylaxis), is protective in more than 90% of patients. ,
b) HBsAg-negative and anti-core positive recipients: in absence of prophylaxis the risk of sero-reversion after transplantation (de-novo hepatitis B) is less than 5% from naοve liver donors and 10-15% from anti-core positive donors. ,
c) HBsAg-positive donors: the risk of hepatitis B transmission with a liver from an HBsAg-positive donor is high, as the neutralizing effect of HBIG is very low in this setting and the reappearance of HDV, in co-infected recipients, is constant. In this particular condition the reactivation of hepatitis would appear to be controlled by the combination of two antivirals in the long term. 
In Italy, the transplantation is controlled by the national guidelines (www.governo.it/GovernoInforma/Dossier/donatori_organi/linee_guida.html);
d) HBsAg-negative/anti-core positive donors: in this category the overall risk of HBV transmission and hepatitis is high (33-78%), in the absence of prophylaxis, ranging from 70% in naοve to 10-15% in anti-core recipients. Combined prophylaxis with lamivudine and HBIG controls relapse in nearly all cases, while personalized prophylaxis with only HBIG or only lamivudine has been suggested in low risk recipients (anti-core positive).  Comparative studies are not available in this setting.
Recommendations in relation to recipients
In all HBsAg-positive carriers there is an indication to universal prophylaxis post-surgery according to their original virological condition:
a) in active carriers, therapy before surgery is indicated (with one or two antivirals in cases of YMDD mutants), with the aim of achieving the reduction of HBV DNA below the limit of sensitive HBV assays or at least below < 20,000 IU/ml, in association with combined prophylaxis (HBIG and one or two antivirals, as previously reported) in the post-operative period;
b) in inactive carriers, the role of therapy before surgery remains controversial because of the high (> 80%) protective effect of post-transplantation combined prophylaxis. In these subjects a preventive reduction of HBV DNA before surgery might not be necessary, with regard to the minimal residual risk, but it could be desirable in order to save HBIG in the long term after liver transplantation. Likewise, in subjects with spontaneous undetectable viremia (PCR-negative) or with levels around the limit of detectability (< 2,000 IU/ml), especially if co-infected with HDV, the protective power of just HBIG seems to be very high. Although also in this condition the use of the combined prophylaxis after liver transplantation permits a considerable saving of HBIG in the long term;
c) in HBsAg-negative/anti-core positive recipients, in analogy with what has been described in the other transplants, albeit in the presence of serum and intra-hepatic evidence of re-infection by HBV in the post-transplant period, the risk of reverse-seroconversion is practically nil , and so there is no indication for any prophylaxis, but only the monitoring of the HBsAg.
Recommendations in relation to donors
As indicated by the national guidelines the use of organs from HBsAg-positive donors should be considered only in conditions of emergency, avoiding their use in HDV recipients. The use of universal prophylaxis with two antivirals post-transplant could permit the control of hepatitis B recurrence in the long term. Instead the use of livers from HBsAg-negative/anti-core positive donors justifies the adherence to the indications reported in Section7.5 and the activation of universal prophylaxis with HBIG and lamivudine in the case of allocation to naοve recipients and with only HBIG or only lamivudine (after the administration of HBIG in the peri-operative period) in anti-core recipients.
Reports regarding the reactivation of HBV in the rheumatology setting are episodic, during the course of hydroxychlorochine, azathioprine, methotrexate and anti-Tumor Necrosis factor (TNF). The few data available all refer to active and inactive HBsAg carriers. However,reports on anti-CD20 derive from hematological experience, and like in hematology the risk of HBV reactivation in the rheumatology setting would appear to be linked both to the phase of immuno-suppression and to that of immuno-reconstitution. In the meantime no reactivations have been reported in the few HBsAg-positive rheumatology patients undergoing universal prophylaxis with lamivudine during immunosuppressive therapy. ,,,
In the absence of data two risk categories have been identified with regard to the type and to the degree of immunosuppression: a) high risk of HBV reactivation in patients undergoing the following therapy: anti-TNF antibodies, medium to high dosage steroids (>7.5 mg/die) for prolonged periods, immunosuppressors such as cyclophosphamide, methotrexate, leflunomide, cyclosporine, tacrolimus, azathioprine and mycophenolate. Although cases of viral reactivation have not yet been described in rheumatology patients undergoing treatment with anti-CD20 antibodies, the data which have emerged in other specialist circles suggest the inclusion in this group of these and other monoclonals; b) low risk of HBV reactivation in patients treated with steroids at <7.5 mg/die, sulfasalazine and hydroxychlorochine.
Among HBsAg-positive patients, therapy is indicated in active carriers and universal prophylaxis with NAs is suggested in inactive carriers who underwent high-risk treatment, especially if they are subjects with manifestations of chronic liver disease due to the previous activity of HBV or other causes. Finally, in inactive HBsAg-carriers treated with low risk therapies and in HBsAg-negative/anti-core positive subjects the proposal is a strategy of monitoring, with the activation of therapy or targeted prophylaxis in the case of viral reactivation (HBV DNA > 20,000 IU/ml) or sero-reversion, respectively.
Prophylaxis should be started 2-4 weeks before the immunosuppressive therapy if possible and continued for at least 6-12 months afterwards (i.e. after immunosuppressive therapy has been suspended). Hematology literature advises particular caution in suspending prophylaxis, especially in subjects treated with repeated cycles of monoclonal antibodies.
Peculiar conditions in the rheumatology setting
Anti-HBV vaccination. Vaccination in rheumatology patients remains controversial and its cost/benefit ratio should be carefully assessed in groups particularly at risk of HBV (for example those living with HBsAg-positive individuals or health workers).
Panarteritis nodosa (PAN). This is a rare necrotizing vasculitis that affects small and medium-sized arteries which presents, at least in a portion of cases, a pathogenic correlation with HBV infection. In the treatment of HBV-related PAN, the immunosuppressive therapy (which also poses the question of an uncontrolled activation of the virus) should be associated with an antiviral therapy (in active carriers) or universal prophylaxis (in inactive carriers) to repress viral replication. In this regard single cases and observational studies with small numbers of cases have documented the efficacy of interferon (IFN) and lamivudine.
The indications, in this setting, refer to the recently published European Association for the Study of the Liver (EASL) guidelines. Cirrhosis and liver cancer are the second cause of death worldwide in HIV carriers (3-4 million), 9% of whom have HBV infection. Co-infection with HIV increases the rate of chronic HBV infection, reduces the annual rate of seroconversion to antiHBe and to antiHBs and may be linked to the reactivation of the occult infection in HBsAg-negative subjects in the presence of severe immuno-depletion. Moreover co-infection with HIV accelerates progression towards cirrhosis and liver decompensation and reduces survival in decompensated cirrhotics. Therefore mortality due to liver disease in those co-infected with HIV-HBV is higher compared to subjects with just HBV infection. ,
A. Patients undergoing Anti-Retroviral Therapy (ART). In active and inactive carriers therapy and universal prophylaxis with antivirals (utilizing the same nucleos(t)ides effective on HBV used in the treatment of HIV infection) are indicated, respectively.
In HBsAg-negative/anti-core positive subjects, the condition of occult carrier, characterized by HBV DNA positivity in serum and/or in the liver, has been identified in 35-90% of subjects with HIV co-infection using high sensitivity techniques, and only in 1% of cases with less sensitive techniques. Even in the presence of anecdotal reports of reactivation during immunodepletion and/or of suspension of lamivudine, the risk of sero-reversion appears to be very low (0.23/100 patients/year) and it does not therefore justify any prophylaxis but only monitoring. 
B. Patients who do not require ART. In active carriers therapy with interferons or antivirals is indicated. In these subjects treatment should preferably be administered using drugs which do not have any effect on HIV and which do not, in the future, induce resistance to ART (interferons, entecavir, telbivudine).
Instead, in inactive carriers and in anti-core subjects monitoringof HBV DNA or HBsAg, respectively, is recommended, with activation of therapy or targeted prophylaxis in the case of reactivation or sero-reversion.
The literature on hepatitis B in immunodepressed patients is heterogeneous. It refers mainly to the pre-analogue nucleos(t)ides era and the period prior to the introduction of the modern techniques of determination and quantification of the viremia, which raises many doubts and difficulties about the interpretation of the studies and leaves several aspects still a matter of debate. This encourages the proposal of a network of communication between different specialists involved, in order to better define the natural history, the potential risk of hepatitis B and the results of the various strategies proposed.
Even in the light of such premises today it appears to be justified to propose a rational approach to the problem of hepatitis B in immunocompromised patients [Table 4], which provides for:
Finally, the greatest uncertainty concerns the most cost-effective management of HBsAg negative/anti-HBc positive (anti-core) subjects. For most of these patients involved in the different settings, a simple monitoring of HBsAg seems to be the most rational approach. In contrast, in those enlisted for HSCT and/or undergoing intense chemotherapy, especially in the presence of multi-cycles of antiCD20 or antiCD52 monoclonal antibodies, universal prophylaxis is considered to be cost-effective and is therefore proposed. However, clinical studies in this setting are scarce and there is an absolute need for these to be conducted in the near future.
- monitoring the markers of the HBV in all subjects starting immunosuppressive therapies and the evaluation of their liver condition (baseline),t
- therapy of active carriers,
- prophylaxis of inactive carriers, especially if they are undergoing immunosuppressive therapies judged to be at high risk. In this case the treatment should be limited to the period of immunosuppression and to the subsequent reconstitution, in the settings in which this is possible (hematology and HSCT, rheumatology, oncology, HIV) and continued indefinitely in the condition of solid organs transplantation,
- biochemical and HBsAg monitoring (or viremia monitoring, when this strategy is chosen) with the aim of activating a swift therapy or a targeted prophylaxis, respectively in inactive carriers and in anti-core subjects not undergoing prophylaxis,
- evaluation, in the transplant setting, of the virological characteristics of both recipients and donors, in order to activate the best prophylactic strategies and to obtain the best allocation in the case of a significant risk of hepatitis B after surgery (organs from donors who are positive for HBsAg or anti-core antibodies).
| Acknowledgements|| |
To Mrs Susan Phillips for the language revision and to Mrs Monica Moretti, Mrs Clara Grossi and Silvia Carenzi, MD, for their valuable assistance in the preparation of the first AISF Single Topic conference and of the manuscript. We want to thank all the scientific associations who endorsed the meeting and the participants in the different groups of discussion and in the plenary session.
| References|| |
|1.||Yeo W, Johnson PJ. Diagnosis, prevention and management of hepatitis B virus reactivation during anticancer therapy. Hepatology 2006, 2006;43:209-20. |
|2.||Raimondo G, Pollicino T, Squadrito G. What is the clinical impact of occult hepatitis B virus infection? 2005;365:638-40. [PUBMED] [FULLTEXT] |
|3.||EASL Jury. EASL International Consensus Conference on Hepatitis B. 13-14 September, 2002: Geneva, Switzerland. Consensus statement (short version). J Hepatol 2003;38:533-40. |
|4.||Keeffe EB, Dieterich DT, Han SH, Jacobson IM, Martin P, Schiff ER, et al. A treatment algorithm for the management of chronic hepatitis B virus infection in the United States. Clin Gastroenterol Hepatol 2004;2:87-106. [PUBMED] [FULLTEXT] |
|5.||Di Marco V, Marzano A, Lampertico P, Andreone P, Santantonio T, Almasio PL, et al. Clinical outcome of HBeAg-negative chronic hepatitis B in relation to virological response to lamivudine. Hepatology 2004;40:883-91. [PUBMED] [FULLTEXT] |
|6.||Fung SK, Chae HB, Fontana RJ, Conjeevaram H, Marrero J, Oberhelman K, et al. Virologic response and resistance to adefovir in patients with chronic hepatitis. J Hepatol 2006;44:283-90. [PUBMED] [FULLTEXT] |
|7.||Locarnini S, Hatzakis A, Heathcote J, Keeffe EB, Liang TJ, Mutimer D, et al. Management of antiviral resistance in patients with chronic hepatitis B. Antivir Ther 2004;9:679-93. [PUBMED] [FULLTEXT] |
|8.||Mutimer D. Adefovir-lamivudine combination therapy and hepatitis B kinetics. J Hepatol 2005;43:200-2. [PUBMED] [FULLTEXT] |
|9.||Mutimer D, Dusheiko G, Barrett C, Grellier L, Ahmed M, Anschuetz G, et al. Lamivudine without HBIg for prevention of graft reinfection by hepatitis B: Long-term follow-up. Transplantation 2000;70:809-15. [PUBMED] [FULLTEXT] |
|10.||Matthews GV, Bartholomeusz A, Locarnini S, Ayres A, Sasaduesz J, Seaberg E, et al. Characteristics of drug resistant HBV in an international collaborative study of HIV-HBV-infected individuals on extended lamivudine-therapy. AIDS 2006;20:863-70. [PUBMED] [FULLTEXT] |
|11.||Lampertico P, Vigano M, Manenti E, Iavarone M, Lunghi G, Colombo M. Adefovir rapidly suppresses hepatitis B in HBeAg-negative patients developing genotypic resistance to lamivudine. Hepatology 2005;42:1414-9. |
|12.||Alexopoulos CG, Vaslamatzis M, Hatzidimitriou G, Prevalence of hepatitis B virus marker positivity and evolution of hepatitis B virus profile, during chemotherapy, in patients with solid tumours. B J Cancer 1999;81:69-74. |
|13.||Marcucci F, Mele A, Spada E, Candido A, Bianco E, Pulsoni A, et al. High prevalence of hepatitis B virus infection in B-cell non-Hodgkin's lymphoma, Haematologica 2006;91:554-7. |
|14.||Takai S, Tsurumi H, Ando K, Kasahara S, Sawada M, Yamada T, et al. Prevalence of hepatitis B and C virus infection in haematological malignancies and liver injury following chemotherapy. Eur J Hematol 2005;74:158-65. |
|15.||Dai MS, Chao TY, Kao WY, Shyu RY, Liu TM. Delayed hepatitis B virus reactivation after cessation of pre-emptivelamivudine in lymphoma patients treated with rituximab plus CHOP. Ann Hematol 2004;83:769-74. [PUBMED] [FULLTEXT] |
|16.||Hui CK, Cheung WW, Au WY, Lie AK, Zhang HY, Yueng YH, et al. Hepatitis B reactivation after withdrawal of pre-emptive lamivudine in patients with haematological malignancy on completion of cytotoxic chemotherapy. Gut 2005;54:1597-603. [PUBMED] [FULLTEXT] |
|17.||Lau GK, Yiu HH, Fong DY, Cheng HC, Au WY, Lai LS, et al. Early is superior to deferred pre-emptive lamivudine therapy for hepatitis B patients undergoing chemotherapy. Gastroenterology 2003;125:1742-9. [PUBMED] [FULLTEXT] |
|18.||Kohrt HE, Ouyang DL, Keeffe EB. Systemic review: Lamivudine prophylaxis for chemotherapy-induced reactivation of chronic hepatitis B virus infection. Aliment Pharmacol Ther 2006;24:1003-6. [PUBMED] [FULLTEXT] |
|19.||Knoll A, Pietrzyk M, Loss M, Goetz WA, Jilg W. Solid organ transplantation in HBsAg-negative patients with antibodies to HBV core antigen: Low risk of HBV reactivation. Transplantation 2005;79:1631-3. |
|20.||Allain JP. Occult hepatitis B virus infection: Implications in transfusion. Vox Sang 2004;86:83-91. [PUBMED] [FULLTEXT] |
|21.||Zekri AR, Mohamed WS, Samra MA, Sherif GM, El-Shehaby AM, El-Sayed MH. Risk factors for cytomegalovirus, hepatitis B and C virus reactivation after bone marrow transplantation. Transpl Immunol 2004;13:305-11. [PUBMED] [FULLTEXT] |
|22.||Dickson RC, Terrault NA, Ishitani M, Reddy KR, Sheiner P, Luketic V, et al. Protective antibody levels and dose requirements for IV 5% Nabi Hepatitis B immune globulin combined with lamivudine in liver transplantation for hepatitis B-induced end stage liver disease. Liver Transpl 2006;12:124-33. [PUBMED] [FULLTEXT] |
|23.||Fabrizi F, Martin P, Dixit V, Kanwal F, Dulai G. HBsAg seropositive status and survival after renal transplantation: Meta-analysis of observational studies. Am J Transplant 2005;5:2913-21. [PUBMED] [FULLTEXT] |
|24.||Berger A, Preiser W, Kachel HG, Sturmer M, Doerr HW. HBV reactivation after kidney transplantation. J Clin Virol 2005;32:162-5. |
|25.||Fagiuoli S, Minniti F, Pevere S, Farinati F, Burra P, Livi U, et al. HBV and HCV infections in heart transplant recipients. J Heart Lung Transplant 2001;20:718-24. [PUBMED] [FULLTEXT] |
|26.||Zampino R, Marrone A, Ragone E, Costagliola L, Cirillo G, Karayiannis P, et al. Heart transplantation in patients with chronic hepatitis B: Clinical evaluation, molecular analysis and effect of treatment. Transplantation 2005;80:1340-3. |
|27.||De Feo TM, Grossi P, Poli F, Mozzi F, Messa P, Minetti E, et al. Kidney transplantation from anti-HBc positive donors: Results from a retrospective Italian study. Transplantation 2006;81:76-80. [PUBMED] [FULLTEXT] |
|28.||Fabrizi F, Dulai G, Dixit V, Bunnapradist S, Martin P. Lamivudine for the treatment of hepatitis B virus-related liver disease after renal transplantation: Meta-analysis of clinical trials. Transplantation 2004;77:859-64. [PUBMED] [FULLTEXT] |
|29.||Fabrizi F, Lunghi G, Martin P. Hepatitis B virus infection in hemodialysis: Recent discoveries. J Nephrol 2002;15:463-8. [PUBMED] [FULLTEXT] |
|30.||Natov SN, Pereira BJ. Transmission of viral hepatitis by kidney transplantation. Transplant Infect Dis 2002;4:117-23. |
|31.||Berber I, Aydin C, Yigit F, Turkmen F, Titiz I, Altaca G. The effect of HBsAg-positivity of kidney donors on long-term patient and graft outcome. Transplant Proc 2005;37:4173-5. |
|32.||Marzano A, Lampertico P, Mazzaferro V, Carenzi S, Vigano M, Romito R, et al. Prophylaxis of hepatitis B virus recurrence after liver transplantation in carriers of lamivudine-resistant mutants. Liver Transpl 2005;11:532-8. [PUBMED] [FULLTEXT] |
|33.||Marzano A, Gaia S, Ghisetti V, Carenzi S, Premoli A, Debernardi-Venon W, et al. Viral load at the time of liver transplantation and risk of hepatitis B virus recurrence. Liver Transpl 2005;11:402-9. [PUBMED] [FULLTEXT] |
|34.||Manzarbeitia C, Reich DJ, Ortiz JA, Rothstein KD, Araya VR, Munoz SJ. Safe use of livers from donors with positive hepatitis B core antibody. Liver Transpl 2002;8:556-61. [PUBMED] [FULLTEXT] |
|35.||Franchello A, Ghisetti V, Marzano A, Romagnoli R, Salizzoni M. Transplantation of hepatitis B surface antigen-positive livers into hepatitis B virus-positive recipients and the role of hepatitis delta coinfection. Liver Transpl 2005;11:922-8. [PUBMED] [FULLTEXT] |
|36.||Ghisetti V, Marzano A, Zamboni F, Barbui A, Franchello A, Gaia S, et al. Occult hepatitis B virus infection in HBsAg negative patients undergoing liver transplantation: Clinical significance. Liver Transpl 2004;10:356-62. [PUBMED] [FULLTEXT] |
|37.||Abdelmalek MF, Pasha TM, Zein NN, Persing DH, Wiesner RH, Douglas DD. Subclinical reactivation of hepatitis B virus in liver transplant recipients with past exposure. Liver Transpl 2003;9:1253-7. [PUBMED] [FULLTEXT] |
|38.||Vento S, Cainelli F, Longhi MS. Reactivation of replication of hepatitis B and C viruses after immunosuppressive therapy: An unresolved issue. Lancet Oncol 2002;3:333-40. [PUBMED] [FULLTEXT] |
|39.||Esteve M, Saro C, Gonzalez-Huix F, Suarez F, Forne M, Viver JM. Chronic hepatitis B reactivation following infliximab therapy in Crohn's disease patients: Need for primary prophylaxis. Gut 2004;53:1363-5. |
|40.||Zanati SA, Locarnini SA, Dowling JP, Angus PW, Dudley FJ, Roberts SK. Hepatic failure due to fibrosing cholestatic hepatitis in a patient with pre surface mutant hepatitis B virus and mixed connective tissue disease treated with prednisolone and chloroquine. J Clin Vir 2004;31:53-7. |
|41.||Calabrese LH, Zein NN, Vassilopoulos D. Hepatitis B reactivation with immunosuppressive therapy in rheumatic disease: Assessment and preventive strategies. Ann Rheum Dis 2006;65:983-9. [PUBMED] [FULLTEXT] |
|42.||Buttgereit F, da Silva JA, Boers M, Burmester GR, Cutolo M, Jacobs J, et al. Standardised nomenclature for glucocorticoid dosages and glucocorticoid treatment regimens: Current questions and tentative answers in rheumatology. Ann Rheum Dis 2002;61:718-22. [PUBMED] [FULLTEXT] |
|43.||Alberti A, Clumeck N, Collins S, Gerlich W, Lundgren J, Palω G, et al. Short statement of the first European Consensus Conference on the treatment of chronic hepatitis B and C in HIV co-infected patients. J Hepatol 2005;42:615-24. |
|44.||Puoti M, Torti C, Bruno R, Filice G, Carosi G. Natural history of chronic hepatitis B in co-infected patients. J Hepatol 2006;44:S65-70. [PUBMED] [FULLTEXT] |
|45.||Firpi R, Nelson D. Management of viral hepatitis in hematologic malignancies. Blood Rev 2008;22:117-26. |
|46.||Katz LH, Fraser A, Gafter-Gvili A, Leibovici L, Tur-Kaspa R. Lamivudine prevents reactivation of hepatitis B and reduces mortality in immunosuppressed patients: Systematic review and meta-analysis. J Viral Hepat 2008;15:89-102. |
|47.||Martyak LA, Taqavi E, Saab S. Lamivudine prophylaxis is effective in reducing hepatitis B reactivation and reactivation-related mortality in chemotherapy patients: A meta-analysis. Liver Int 2007;:28-38. [PUBMED] [FULLTEXT] |
|48.||Saab S, Dong MH, Joseph TA, Tong MJ, Hepatitis B prophylaxis in patients undergoing chemotherapy for lymphoma: A decision analysis model. Hepatology 2007;46:1049-56. |
|49.||Yeo W, Chan PK, Ho WM, Zee B, Lam KC, Lei KL, et al. Lamivudine for the prevention of hepatitis B virus reactivation in hepatitis B s-antigen seropositive cancer patients undergoing cytotoxic chemotherapy, J Clin Oncol 2004;22:927-34. |
|50.||Li YH, He YF, Jiang WQ, Wang FH, Lin XB, Zhang L, et al. Lamivudine prophylaxis reduces the incidence and severity of hepatitis in hepatitis b virus carriers who receive chemotherapy for lymphoma. Cancer 2006;106:1320-5. [PUBMED] [FULLTEXT] |
|51.||Aksoy S, Harputluoglu H, Kilickap S, Dede DS, et al. Rituximab-related viral infections in lymphoma patients. Leuk Lymph 2007;48:1307-12. |
|52.||Targhetta C, Cabras MG, Mamusa AM, Mascia G, Angelucci E. Hepatitis B virus related disease in isolated anti-Hepatitis B-core positive lymphoma patients receiving chemo or chemo-immune therapy. Haematologica 2008;93:951-2. [PUBMED] [FULLTEXT] |
|53.||Hui CK, Cheung WW, Leung KW, Cheng VC, Tang BS, Li IW, et al. Outcome and immune reconstitution of HBV-specific immunity in patients with reactivation of occult HBV infection after alemtuzumab-containing chemotherapy regimen. Hepatology 2008;48:1-10. [PUBMED] [FULLTEXT] |
|54.||Tavil B, Kuskonmaz B, Kasem M, Demir H, Cetin M, Uckan D. Hepatitis B immunoglobulin in combination with lamivudine for prevention of hepatitis B virus reactivation in children undergoing bone marrow transplantation. Pediatr Transplant 2006;10:966-9. |
|55.||Sobhonslidsuk A, Ungkanont A. A prophylactic approach for bone marrow transplantation from a hepatitis B surface antigen-positive donor. World J Gastroenterol 2007;13:1138-40. [PUBMED] [FULLTEXT] |
Division of Gastroenterology, AOU San Giovanni Battista, Corso Bramante 88, 10125, Torino
Source of Support: None, Conflict of Interest: None
[Table 1], [Table 2], [Table 3], [Table 4]
|This article has been cited by|
||Risk of hepatitis B infection in pediatric acute lymphoblastic leukemia in a tertiary care center from South India
| ||B. Guruprasad,S. Kavitha,B.S. Aruna Kumari,B.R. Vijaykumar,B.G. Sumati,Sinha Mahua,L. Appaji,R.S. Jayshree |
| ||Pediatric Blood & Cancer. 2014; : n/a |
|[Pubmed] | [DOI]|
| Article Access Statistics|
| Viewed||13750 |
| Printed||535 |
| Emailed||6 |
| PDF Downloaded||916 |
| Comments ||[Add] |
| Cited by others ||1 |