Can a kidney donor who is anti‑HBc total positive donate a kidney?

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Last updated: February 23, 2026View editorial policy

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Can Anti-HBc Total Positive Donors Donate Kidneys?

Yes, anti-HBc total positive donors can safely donate kidneys, and this practice is explicitly supported by consensus guidelines to expand the donor pool. 1

Evidence Supporting Anti-HBc Positive Kidney Donation

The American Society of Transplantation consensus guidelines explicitly state that HBV-positive donors (including anti-HBc positive donors) should be considered for donation to safely expand the organ pool. 2 The key data supporting this practice includes:

  • In a review of 1,385 HBsAg-negative kidney recipients from anti-HBc+ donors, the rate of HBsAg acquisition was only 0.28% (4/1385) with no evidence of symptomatic hepatitis. 1

  • Patient and graft outcomes were not worse among patients with HBsAg acquisition or evidence of anti-HBs or anti-HBc seroconversion. 1

  • The largest UNOS database study showed HBsAg acquisition occurred at similar rates from anti-HBc+ donors (0.001 cases per year) compared to anti-HBc-negative donors (0.003 cases per year). 1

Risk Stratification Based on Recipient Status

The transmission risk and management strategy depends critically on the recipient's HBV immunity status:

Recipients with HBV Immunity (Anti-HBs+ or Prior HBV)

  • Clinical hepatitis has not been noted in immunized individuals following kidney transplantation from anti-HBc+ donors, possibly due to partial protection from vaccination. 1
  • No prophylaxis is typically required for immune recipients. 1
  • These recipients can safely receive anti-HBc+ kidneys without significant transmission risk. 3

HBV-Naive Recipients (No Prior Exposure or Vaccination)

  • HBV vaccination prior to transplant with target anti-HBs titers >10 IU/L has been demonstrated to be protective for renal recipients of anti-HBc+ donors. 1
  • Higher antibody titers provide better protection: risk of anti-HBc seroconversion was 4% when anti-HBs titers were >100 IU/L compared to 10% when <100 IU/L. 1
  • In one observational study of 46 kidney recipients from anti-HBc+ organs, there was no evidence of HBV transmission after a median of 36 months when non-immune recipients were treated with lamivudine for 1 year. 1

HBsAg-Positive Recipients

  • Kidneys from anti-HBc+ donors can be successfully transplanted into HBsAg+ recipients with appropriate antiviral coverage. 4
  • These recipients already require long-term antiviral therapy regardless of donor status. 4

Recommended Management Algorithm

Step 1: Confirm Donor Serologic Status

  • Verify donor is HBsAg-negative and anti-HBc total positive. 1, 2
  • Additional testing for anti-HBs status in the donor does not impact transmission risk but may be performed. 1

Step 2: Assess Recipient HBV Status

  • Check recipient HBsAg, anti-HBs, anti-HBc, and HBV DNA levels. 4
  • Measure quantitative anti-HBs titers if recipient has been vaccinated. 1

Step 3: Implement Risk-Stratified Prophylaxis

  • If recipient is HBV-immune (anti-HBs >10 IU/L): No prophylaxis required; proceed with transplantation. 1
  • If recipient is HBV-naive: Either vaccinate pre-transplant to achieve anti-HBs >10 IU/L (preferably >100 IU/L) OR provide antiviral prophylaxis (lamivudine for 1 year or entecavir/tenofovir). 1
  • If recipient is HBsAg-positive: Continue or initiate long-term antiviral therapy with entecavir or tenofovir. 4

Step 4: Post-Transplant Monitoring

  • Monitor for HBsAg and HBV DNA at regular intervals (6,12,24, and 36 months). 1
  • Check for anti-HBc or anti-HBs seroconversion. 1

Critical Distinctions from Liver Transplantation

The risk profile for kidney transplantation from anti-HBc+ donors is fundamentally different from liver transplantation:

  • Transmission risk is significantly lower in kidney recipients compared to liver recipients. 1, 5
  • No HBV transmission was observed in kidney recipients from anti-HBc+ donors independent of recipient immunological profile in multiple studies. 5
  • In contrast, liver recipients show a 43% de novo hepatitis rate in naive patients without prophylaxis. 5

Common Pitfalls to Avoid

Do not reject anti-HBc+ kidney donors automatically. This unnecessarily discards viable organs when safe use protocols exist. 1, 2, 3

Do not use HBIG routinely in kidney recipients. There is likely no role for HBIG in the setting of antiviral prophylaxis, and data demonstrating benefit in kidney recipients are lacking. 1

Do not use lamivudine as first-line if choosing antiviral prophylaxis. While lamivudine has been studied extensively, entecavir and tenofovir have superior resistance profiles. 1, 4

Do not assume isolated anti-HBc positivity always represents true HBV exposure. False-positive results can occur and should be considered, though this does not change the safety of proceeding with donation. 6

Do not confuse anti-HBc+ donors with HBsAg+ donors. HBsAg-positive donors carry much higher transmission risk and are generally contraindicated except for HBsAg-positive recipients or those with protective immunity. 2, 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Interpretation of Infectious Disease Test Results for Organ Donation Eligibility

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Transmission of viral hepatitis by kidney transplantation: donor evaluation and transplant policies (Part 1: hepatitis B virus).

Transplant infectious disease : an official journal of the Transplantation Society, 2002

Guideline

Kidney Transplantation in Hepatitis B Positive Recipients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Significance of anti-HBc alone serological status in clinical practice.

The lancet. Gastroenterology & hepatology, 2017

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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