Abstract:Long-term HBIg prophylaxis or lamivudine prophylaxis can reduce the risk for hepatitis B virus recurrence. Long-term high-dose HBIg combined with lamivudine can further reduce HBV recurrence to less than 10%.
“…Since the immunologic benefit was not paid with an increased risk of infections, these data obviously indicated beneficial immuno-balancing capabilities of HBIg [67] . In contrast, the risk of bacterial infections was significantly higher in 21 patients with alcoholic liver cirrhosis (P < 0.05), although their immunologic outcome was comparable to that of HBV-positive liver recipients (Table 1).…”
Section: Effects On B-cellsmentioning
confidence: 87%
“…Besides producing significant costs, longterm HBIg monotherapy may promote the development of viral mutations [62,63] . Therefore, a combination of HBIg with potent nucleos(t)ide analogues (NA) is considered as gold standard in prophylaxis of recurrent HBV [62][63][64][65][66][67] . Currently, the combination of anti-HBs Ig with tenofovir or entecavir is under clinical evaluation [62,68] .…”
Shortage of appropriate donor grafts is the foremost current problem in organ transplantation. As a logical consequence, waiting times have extended and pretransplant mortality rates were significantly increasing.
“…Since the immunologic benefit was not paid with an increased risk of infections, these data obviously indicated beneficial immuno-balancing capabilities of HBIg [67] . In contrast, the risk of bacterial infections was significantly higher in 21 patients with alcoholic liver cirrhosis (P < 0.05), although their immunologic outcome was comparable to that of HBV-positive liver recipients (Table 1).…”
Section: Effects On B-cellsmentioning
confidence: 87%
“…Besides producing significant costs, longterm HBIg monotherapy may promote the development of viral mutations [62,63] . Therefore, a combination of HBIg with potent nucleos(t)ide analogues (NA) is considered as gold standard in prophylaxis of recurrent HBV [62][63][64][65][66][67] . Currently, the combination of anti-HBs Ig with tenofovir or entecavir is under clinical evaluation [62,68] .…”
Shortage of appropriate donor grafts is the foremost current problem in organ transplantation. As a logical consequence, waiting times have extended and pretransplant mortality rates were significantly increasing.
“…The superiority of combination HBIG and antiviral prophylaxis was demonstrated in two recent meta-analyses where the rate of recurrent HBV infection was found to be less than 10% in patients that received combination therapy, compared to 4% to 65% in patients given HBIG alone and 4% to 40% in patients given LAM alone [26,27]. These findings were also confirmed in a large, singlecenter retrospective cohort of 1524 patients by Hwang et al [28•] where none of the patients who were given combination prophylaxis developed recurrent HBV, compared to 9.8% of patients given HBIG over 10 years.…”
Section: Post-transplant: Prevention Of Recurrent Hbv Infectionmentioning
Patients who undergo liver transplantation (LT) for chronic hepatitis B virus (HBV) infection are at high risk of developing recurrent HBV in the absence of effective prophylaxis. Pre-LT management should focus on suppression of HBV DNA levels, which have been associated with HBV recurrence. Evidence linking hepatocellular carcinoma (HCC) recurrence to HBV recurrence has been less clear. Prophylaxis against recurrent HBV after LT with combination HBIG and antiviral therapy is the current standard of care and is effective in >90% of patients, but investigation is ongoing to determine the most cost-effective treatment regimens. While antiviral therapy with newer nucleos(t)ide analogues without HBIG is assumed to be effective, no recent studies have examined the long-term efficacy of salvage regimens for recurrent HBV. Large, prospective trials are urgently needed. Overall, LT for HBV is highly effective with appropriate pre-and post-LT antiviral therapy.
“…In the mid 1990s, Lamivudine (LAM), the first oral antiviral agent for HBV, in addition to hepatitis B immunoglobulin (HBIG) revolutionized the treatment of HBV. Long-term high-dose HBIG combined with LAM can reduce HBV recurrence to less than 10% (Chen, Yi et al 2010). However, combined treatment with HBIG and LAM is sometimes unable to control recurrent HBV infection.…”
Section: Epidemiology and Specific Risk Factorsmentioning
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