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Transplant donor-recipient HBV status

Transplant donor-recipient HBV status
Donor HBV status Recipient HBV serologic status Kidney transplantation: Whether "to proceed" or "not to proceed" Antiviral therapy* Comments
Chronic infection No evidence of immunity or infection Avoid transplantation except in exceptional circumstances Yes, if transplanted
  • May administer hepatitis B immune globulin in addition to antiviral therapy to prevent de novo infection.
  • Recipients should be vaccinated if they have no prior immunity, although the efficacy in eliciting an anti-HBs response is reduced due to the effect of immunosuppressive medications.
  • The optimal duration of antiviral therapy is unknown; we administer therapy for 1 year.
Immunity due to vaccination (anti-HBs ≥10 mIU/mL) Yes Yes
  • Administer antiviral therapy to prevent de novo infection because anti-HBs titer can decrease and become undetectable with immunosuppression.
  • The role of hepatitis B immunoglobulin is uncertain but may be considered perioperatively if the anti-HBs level is below 100 mIU/mL.
  • In recipients with immunity from vaccination, we check the anti-HBs titer prior to discontinuing antiviral therapy and administer a booster dose of vaccine if the titer is <10 mIU/mL.
  • The optimal duration of antiviral therapy is unknown; we administer therapy for 1 year.
Prior infection Yes Yes
  • Recipients who are anti-HBc positive have evidence of prior infection, and HBV reactivation may occur secondary to immunosuppressive therapy. The presence of anti-HBs at time of transplantation may not prevent reactivation, because anti-HBs titer can decrease and become undetectable with immunosuppression.
  • The duration of antiviral therapy can vary. Some centers administer antiviral therapy indefinitely to all recipients with prior HBV. Others discontinue treatment when immunosuppression is reduced to low-dose maintenance level and monitor closely thereafter, unless the patient is receiving immunosuppression with an agent associated with a high risk of HBV reactivation (eg, rituximab).
Chronic infection Yes Yes
  • Administer lifelong antiviral therapy to prevent reactivation of HBV secondary to immunosuppressive therapy.Δ
Prior infection No evidence of immunity or infection Yes No, unless donor has detectable HBV viral load
  • Recipients should be vaccinated if they have no prior immunity, although the efficacy in eliciting an anti-HBs response is reduced due to the effect of chronic kidney disease and immunosuppressive medications.
  • If antiviral therapy is administered, the optimal duration is unknown; we administer therapy for 1 year.
Immunity due to vaccination (anti-HBs ≥10 mIU/mL) Yes No, unless donor has detectable HBV viral load
  • If antiviral therapy is administered, the optimal duration of antiviral therapy is unknown; we administer therapy for 1 year.
  • In recipients with immunity from vaccination, we check the anti-HBs titer prior to discontinuing antiviral therapy and administer a booster dose of vaccine if the titer is <10 mIU/mL.
Prior infection Yes Yes
  • Recipients who are anti-HBc positive have evidence of prior infection and need antiviral therapy to prevent HBV reactivation secondary to immunosuppressive therapy. The presence of anti-HBs at time of transplantation may not prevent reactivation, because anti-HBs titer can decrease and become undetectable with immunosuppression.
  • The duration of antiviral therapy can vary. Some centers administer antiviral therapy indefinitely to all recipients with prior HBV. Others discontinue treatment when immunosuppression is reduced to low-dose maintenance level and monitor closely thereafter, unless the patient is receiving immunosuppression with an agent associated with a high risk of HBV reactivation (eg, rituximab).
Chronic infection Yes Yes
  • Administer life-long antiviral therapy to prevent reactivation of HBV secondary to immunosuppressive therapy.Δ
No evidence of prior infection No evidence of immunity or infection Yes No  
Immunity due to vaccination Yes No  
Prior infection Yes Yes
  • Recipients who are anti-HBc positive have evidence of prior infection and may need antiviral therapy to prevent HBV reactivation secondary to immunosuppressive therapy. The presence of anti-HBs at time of transplantation may not prevent reactivation, because anti-HBs titer can decrease and become undetectable with immunosuppression.
  • The duration of antiviral therapy can vary. Some centers administer antiviral therapy indefinitely to all recipients with prior HBV. Others discontinue treatment when immunosuppression is reduced to low-dose maintenance level and monitor closely thereafter, unless the patient is receiving immunosuppression with an agent associated with a high risk of HBV reactivation (eg, rituximab).
Chronic infection Yes Yes
  • Administer life-long antiviral therapy to prevent reactivation of HBV secondary to immunosuppressive therapy.Δ
This table should be used in conjunction with UpToDate content that discusses HBV infection in kidney transplant recipients.
Definitions:
  • No evidence of prior immunity or infection: HBsAg negative, anti-HBc negative, anti-HBs negative
  • Immunity due to vaccination: HBsAg negative, anti-HBc negative, anti-HBs positive
  • Chronic HBV infection: HBsAg positive
  • Prior HBV infection: HBsAg negative, anti-HBc positive
HBV: hepatitis B virus; anti-HBs: hepatitis B surface antibody; mIU: milli-international units; anti-HBc: hepatitis B core antibody; HBsAg: hepatitis B surface antigen.
* Entecavir or tenofovir alafenamide is the preferred antiviral agent.
¶ Some centers may also factor the HBV DNA status of the donor in the decision to administer antiviral therapy.
Δ Refer to UpToDate topics on how to prevent HBV reactivation in patients receiving immunosuppressive therapy.
If the donor is anti-HBc negative and anti-HBs positive, the donor is immune because of vaccination, not past infection.
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