What is the significance of a Hepatitis B surface antibody level of 0.36 IU/L in an 18-year-old male (YOM) with previously treated Hepatitis B (hep B) and normal liver function tests, including aspartate aminotransferase (AST), alanine aminotransferase (ALT), C-reactive protein (CRP), and gamma-glutamyl transferase (GGT)?

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Last updated: May 5, 2025View editorial policy

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From the Guidelines

This 18-year-old male requires hepatitis B vaccination due to his inadequate immunity, as indicated by a hepatitis B surface antibody level of 0.36 IU/L, which is below the protective level of ≥10 IU/L 1. Given his history of hepatitis B treatment and current low antibody level, he is at risk of reinfection, which could lead to more severe liver damage.

  • His normal liver function tests (AST, ALT, GGT) and inflammatory markers (CRP) do not negate the need for vaccination, as the primary concern is preventing future infection.
  • The hepatitis B vaccine is safe and highly effective, with protection rates over 95% in young adults who complete the full series 1.
  • He should receive a complete hepatitis B vaccination series consisting of three doses: the initial dose, followed by a second dose 1 month later, and a third dose 6 months after the first.
  • After completing the series, antibody levels should be checked 1-2 months later to confirm immunity, as some individuals may not respond to the vaccine and require additional doses or alternative approaches 1.
  • It is essential to note that, according to the Advisory Committee on Immunization Practices (ACIP), persons who do not respond to a primary 3-dose vaccine series may respond to an additional vaccine dose or a 3-dose revaccination series, but more than two vaccine series are not recommended in nonresponders 1.

From the FDA Drug Label

Antibody titers ≥10 mIU/mL against HBsAg are recognized as conferring protection against hepatitis B. The patient's hepatitis B surface antibody is 0.36 IU/L, which is below the protective level of ≥10 mIU/mL.

  • The patient is not protected against hepatitis B.
  • Booster vaccination may be necessary to achieve protective antibody levels 2, 2.

From the Research

Hepatitis B Surface Antibody Levels

  • The patient's hepatitis B surface antibody level is 0.36 IU/L, which is considered low 3.
  • A study from 1985 found that isolated anti-HBs levels were low and did not persist, and the immunologic specificity and protective value of anti-HBs, especially when levels are low, remain questionable 3.
  • Another study from 2014 found that viral clearance can be achieved for high anti-HBV antibody levels, but the mechanism of protection is complex and depends on various factors, including the rate of synthesis of hepatitis B subviral particles and the rate of anti-HBV antibody production 4.

Protective Levels of Hepatitis B Surface Antibody

  • A study from 2020 found that the prevalence of protective levels of hepatitis B surface antibody (anti-HBs) among adults at high risk of HBV infection was around 23.4%, and the prevalence increased from 2003-2006 to 2007-2010, but no change occurred from 2007-2010 to 2011-2014 5.
  • The same study found that factors associated with positive anti-HBs serology included young age and higher education 5.
  • A study from 2023 found that hepatitis B vaccination in patients after HBsAg seroclearance increased the anti-HBs seroconversion rate and significantly increased antibody levels, with good safety 6.

Clinical Significance of Antibody to Hepatitis B Surface Antigen

  • A study from 2025 found that anti-HBs is recognized as a protective immune marker, both for HBV infection clearance and following vaccination, and it is also considered an important indicator of functional cure for CHB 7.
  • The same study found that the restoration of HBV-specific B cell function, along with the induction of an anti-HBs antibody response, is regarded as pivotal for terminating chronic HBV infection and achieving functional cure 7.

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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