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Published on: September 25, 2019
Four-year follow up of hepatitis C patients vaccinated against hepatitis B virus
Slawomir Chlabicz1, Tadeusz-Wojciech Lapinski, Anna Grzeszczuk
1Mieszka I 4B 15-054 Bialystok, Poland. schlabicz@poczta.onet.pl
Insights
Four years after hepatitis B vaccination, over 60% of chronic hepatitis C patients lacked protective antibody levels, increasing their risk for hepatitis B virus infection. Further research is needed to assess long-term immune memory.
Area of Science:
- Hepatology
- Immunology
- Vaccinology
Background:
- Patients with chronic hepatitis C (HCV) are recommended for hepatitis B vaccination.
- Assessing long-term immunogenicity and efficacy of hepatitis B vaccination in HCV patients is crucial.
Purpose of the Study:
- To evaluate hepatitis B immunogenicity and efficacy 4 years post-primary immunization in chronic hepatitis C patients.
- To determine if hepatitis C virus infection impacts the sustained antibody response to hepatitis B vaccination.
Main Methods:
- 36 chronic hepatitis C patients vaccinated with recombinant HBsAg (20 μg) on a 0-1-6 month schedule were studied.
- Anti-HBs and anti-HBc titers were measured 4 years after the third vaccine dose.
- A control group of 10 healthy individuals was included for comparison.
Main Results:
- Only 36% of hepatitis C patients maintained seroprotective anti-HBs titers after 4 years, compared to 90% in controls (P<0.05).
- Mean anti-HBs concentration was significantly lower in hepatitis C patients (18.3 mIU/mL) than in controls (156.0 mIU/mL) (P<0.05).
- No breakthrough hepatitis B virus infections were observed in either group, confirmed by negative anti-HBc.
Conclusions:
- A significant proportion of vaccinated chronic hepatitis C patients (>60%) lose seroprotective antibody levels 4 years after hepatitis B immunization.
- Inadequate anti-HBs titers may increase the risk of clinically significant breakthrough hepatitis B infections in this population.
- Further studies are needed to investigate the role of B and T lymphocyte memory in providing protection in the absence of adequate antibody titers.
Aim:
Patients with chronic hepatitis C have been recommended to receive vaccinations against hepatitis B. Our study aimed at evaluating the hepatitis B immunogenicity and efficacy against hepatitis B virus infection 4 years after primary immunization series in a group of patients with chronic hepatitis C.
Methods:
We recruited 36 out of 48 hepatitis C virus (HCV) infected individuals who were vaccinated against hepatitis B virus (20 mug of recombinant HBsAg at 0-1-6 mo schedule) in 1998. Here we measured anti-HBs titers and anti-HBc 4 years after delivery of the third dose of primary immunization series.
Results:
After 4 years a total of 13/36 (36%) HCV infected patients had seroprotective titers of anti-HBs compared with 9/10 (90%) in the control group, (P<0.05). Similarly the mean concentration of anti-HBs found in hepatitis C patients was significantly lower than that found in healthy subjects (18.3 and 156.0 mIU/mL respectively (P<0.05). None of the HCV infected patients or controls became infected with HBV during the study period as confirmed by anti-HBc negativity.
Conclusion:
We demonstrated that 4 years after HBV immunizations' more than 60% of vaccinated HCV patients did not maintain seroprotective levels of anti-HBs, which might put them at risk of clinically significant breakthrough infections. Further follow-up studies are required to clarify whether memory B and T lymphocytes can provide protection in chronic hepatitis C patients in the absence or inadequate titers of anti-HBs.
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