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COVID-19 Vaccination Alters NK Cell Dynamics and Transiently Reduces HBsAg Titers Among Patients With Chronic
Hyunjae Shin1, Ha Seok Lee2, Ji Yun Noh3
1Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul 03080, Korea.
Insights
COVID-19 vaccination transiently reduced hepatitis B surface antigen (HBsAg) levels in chronic hepatitis B patients and decreased NKG2A+ NK cells in healthy volunteers. These immune changes were temporary, with HBsAg levels returning to baseline within 180 days.
Area of Science:
- Immunology
- Hepatology
- Vaccinology
Background:
- Coronavirus disease 2019 (COVID-19) vaccination may induce non-specific immune alterations.
- Chronic hepatitis B (CHB) patients on antiviral therapy have specific immune profiles.
- Understanding vaccine impacts on CHB patients is crucial for managing liver disease and immune response.
Purpose of the Study:
- To evaluate the effect of COVID-19 vaccination on hepatitis B surface antigen (HBsAg) levels in CHB patients.
- To assess the impact of COVID-19 vaccination on natural killer (NK) cell dynamics in healthy volunteers.
- To determine if COVID-19 vaccination influences host immunity in the context of CHB.
Main Methods:
- Analysis of serial HBsAg measurements in 2,797 CHB patients before and after COVID-19 vaccination.
- Prospective collection of serial blood samples from 25 healthy volunteers for NK cell analysis.
- Flow cytometry used to examine NK cell populations, specifically NKG2A expression.
Main Results:
- COVID-19 vaccinated CHB patients showed a significant, transient decline in HBsAg levels within 30 days post-vaccination (-21.4 IU/ml), with levels reverting by 91-180 days.
- The velocity of HBsAg decline was transiently accelerated post-vaccination.
- A significant decrease in NKG2A+ NK cells was observed within 7 days after the first COVID-19 vaccine dose in healthy volunteers.
Conclusions:
- COVID-19 vaccination induces a rapid, temporary reduction in HBsAg titers in CHB patients.
- COVID-19 vaccination transiently decreases the frequency of NKG2A+ NK cells, indicating a short-term modulation of innate immunity.
- These findings highlight the transient immunomodulatory effects of COVID-19 vaccines on both liver-specific antigens and innate immune cells.
Abstract:
Coronavirus disease 2019 (COVID-19) vaccination may non-specifically alter the host immune system. This study aimed to evaluate the effect of COVID-19 vaccination on hepatitis B surface Ag (HBsAg) titer and host immunity in chronic hepatitis B (CHB) patients. Consecutive 2,797 CHB patients who had serial HBsAg measurements during antiviral treatment were included in this study. Changes in the HBsAg levels after COVID-19 vaccination were analyzed. The dynamics of NK cells following COVID-19 vaccination were also examined using serial blood samples collected prospectively from 25 healthy volunteers. Vaccinated CHB patients (n=2,329) had significantly lower HBsAg levels 1-30 days post-vaccination compared to baseline (median, -21.4 IU/ml from baseline), but the levels reverted to baseline by 91-180 days (median, -3.8 IU/ml). The velocity of the HBsAg decline was transiently accelerated within 30 days after vaccination (median velocity: -0.06, -0.39, and -0.04 log10 IU/ml/year in pre-vaccination period, days 1-30, and days 31-90, respectively). In contrast, unvaccinated patients (n=468) had no change in HBsAg levels. Flow cytometric analysis showed that the frequency of NK cells expressing NKG2A, an NK inhibitory receptor, significantly decreased within 7 days after the first dose of COVID-19 vaccine (median, -13.1% from baseline; p<0.001). The decrease in the frequency of NKG2A+ NK cells was observed in the CD56dimCD16+ NK cell population regardless of type of COVID-19 vaccine. COVID-19 vaccination leads to a rapid, transient decline in HBsAg titer and a decrease in the frequency of NKG2A+ NK cells.
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