Prevention of recurrent hepatitis B virus infection after liver transplantation: hepatitis B immunoglobulin, antiviral drugs, or both? Systematic review and meta-analysis
Abstract:Combination treatment with HBIg and LAM reduced HBV recurrence following liver transplantation, compared with HBIg or LAM alone, and reduced mortality compared with HBIg alone.
“…3,4 Hepatitis B immunoglobulin (HBIG) is also important in the management of HBV infection. 5,6 Since vertical transmission is responsible for about 40%-50% of HBV carriers, 5 newborns of mothers who are HBV surface antigen (HBsAg)-positive are generally required to receive HBIG and hepatitis B vaccine within 24 h following delivery and complete the whole regimen of recommended vaccination injections. 7 Liver transplantation is an effective method for end-stage liver disease management, and many people with liver diseases related to HBV receive liver transplantation.…”
Hepatitis B immunoglobulin (HBIG) is important in the management of hepatitis B virus (HBV) infection. Aiming to develop recombinant monoclonal antibodies as an alternative to HBIG, we report the successful identification of HBV surface antigen (HBsAg)-specific antibodies from a full-length human antibody library displayed on mammalian cell surface. Using total RNA of peripheral blood mononuclear cells of a natively immunized donor as template, the antibody repertoire was amplified. Combining four-way ligation and the Flp recombinase-mediated integration (Flp-In) system, we constructed a mammalian cell-based, fully human, full-length antibody display library in which each cell displayed only one kind of antibody molecule. By screening the cell library using fluorescence-activated cell sorting (FACS), eight cell clones that displayed HBsAg-specific antibodies on cell surfaces were identified. DNA sequence analysis of the antibody genes revealed three unique antibodies. FACS data indicated that fluorescent strength of expression (FSE), fluorescent strength of binding (FSB) and relative binding ability (RBA) were all different among them. These results demonstrated that by using our antibody mammalian display and screening platform, we can successfully identify antigen-specific antibodies from an immunized full-length antibody library. Therefore, this platform is very useful for the development of therapeutic antibodies.
“…3,4 Hepatitis B immunoglobulin (HBIG) is also important in the management of HBV infection. 5,6 Since vertical transmission is responsible for about 40%-50% of HBV carriers, 5 newborns of mothers who are HBV surface antigen (HBsAg)-positive are generally required to receive HBIG and hepatitis B vaccine within 24 h following delivery and complete the whole regimen of recommended vaccination injections. 7 Liver transplantation is an effective method for end-stage liver disease management, and many people with liver diseases related to HBV receive liver transplantation.…”
Hepatitis B immunoglobulin (HBIG) is important in the management of hepatitis B virus (HBV) infection. Aiming to develop recombinant monoclonal antibodies as an alternative to HBIG, we report the successful identification of HBV surface antigen (HBsAg)-specific antibodies from a full-length human antibody library displayed on mammalian cell surface. Using total RNA of peripheral blood mononuclear cells of a natively immunized donor as template, the antibody repertoire was amplified. Combining four-way ligation and the Flp recombinase-mediated integration (Flp-In) system, we constructed a mammalian cell-based, fully human, full-length antibody display library in which each cell displayed only one kind of antibody molecule. By screening the cell library using fluorescence-activated cell sorting (FACS), eight cell clones that displayed HBsAg-specific antibodies on cell surfaces were identified. DNA sequence analysis of the antibody genes revealed three unique antibodies. FACS data indicated that fluorescent strength of expression (FSE), fluorescent strength of binding (FSB) and relative binding ability (RBA) were all different among them. These results demonstrated that by using our antibody mammalian display and screening platform, we can successfully identify antigen-specific antibodies from an immunized full-length antibody library. Therefore, this platform is very useful for the development of therapeutic antibodies.
“…20 The combination of HBIg and NAs is more effective against HBV reinfection after liver transplant than HBIg alone, because of synergistic activity; the combination results in a greater reduction in the needed time course and doses of HBIg. 11,21 The combination of HBIg and lamivudine has been the standard of care recommended by many centers against HBV reinfection, with recurrence rate of less than 10% at 2 years after liver transplant. 22 However, there is an increasing interest among liver transplant centers in using more potent NAs, such as adefovir, tenofovir and entecavir, instead of lamivudine.…”
Section: Discussionmentioning
confidence: 99%
“…9,10 Hepatitis B immunoglobulin prophylaxis in combination with the nucleoside/nucleotide analogs (NAs) lamivudine or tenofovir is a well-accepted treatment recommended by many centers for prevention of HBV reinfection after liver transplants. 11 However, there is no consensus on a standard prophylactic method, and controversy over the duration, dose, and route of administration of HBIg exists among transplant centers.…”
Objectives: Hepatitis B immunoglobulin prophylaxis in combination with antiviral drugs is recommended for prevention of hepatitis B virus reinfection after liver transplant. However, there is no consensus on a standard prophylactic method, and controversy exists over the duration, dose, and route of administration. We conducted a prospective study to evaluate the safety and effectiveness of intramuscular hepatitis B immunoglobulin in combination with lamivudine and/or tenofovir and discontinuation of hepatitis B immunoglobulin after 1 year for prevention of hepatitis B virus reinfection.
“…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.
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