Cited by 101Hepatitis B Virus StudiesHepatitis C virus researchIntramuscular injections and effects

A longitudinal hepatitis B vaccine cohort demonstrates long-lasting hepatitis B virus (HBV) cellular immunity despite loss of antibody against HBV surface antigen.

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Simons, Brenna C., Spradling, Philip R., Bruden, Dana J. T., Zanis, Carolyn, Case, Samantha, Choromanski, Tammy L., Apodaca, Minjun, Brogdon, Hazel D. +7 more·2016·Journal of Infectious Diseases

Abstract

BACKGROUND: Long-lasting protection resulting from hepatitis B vaccine, despite loss of antibody against hepatitis B virus (HBV) surface antigen (anti-HBs), is undetermined. METHODS: We recruited persons from a cohort vaccinated with plasma-derived hepatitis B vaccine in 1981 who have been followed periodically since. We performed serological testing for anti-HBs and microRNA-155 and assessed HBV-specific T-cell responses by enzyme-linked immunospot and cytometric bead array. Study subgroups were defined 32 years after vaccination as having an anti-HBs level of either ≥10 mIU/mL (group 1; n = 13) or <10 mIU/mL (group 2; n = 31). RESULTS: All 44 participants, regardless of anti-HBs level, tested positive for tumor necrosis factor α, interleukin 10, or interleukin 6 production by HBV surface antigen-specific T cells. The frequency of natural killer T cells correlated with the level of anti-HBs (P = .008). The proportion of participants who demonstrated T-cell responses to HBV core antigen varied among the cytokines measured, suggesting some natural exposure to HBV in the study group. No participant had evidence of breakthrough HBV infection. CONCLUSIONS: Evidence of long-lasting cellular immunity, regardless of anti-HBs level, suggests that protection afforded by primary immunization with plasma-derived hepatitis B vaccine during childhood and adulthood lasts at least 32 years.

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  1. [32]Werner JM, Abdalla A, Gara N, Ghany MG, Rehermann B. Innate and adaptive immune responses correlate to antibody recall responses to hepatitis B booster vaccineation. Hepatology 2013; 58:612A–3. [Google Scholar]

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Authors
Simons, B. C., Spradling, P. R., Bruden, D. J. T., Zanis, C., Case, S., Choromanski, T. L., Apodaca, M., Brogdon, H. D., Dwyer, G., Snowball, M., Negus, S., Bruce, M. G., Morishima, C., Knall, C., & McMahon, B. J.
Affiliations
  • Centers for Disease Control and Prevention (US)
  • Alaska Native Tribal Health Consortium (US)
  • University of Washington (US)
  • University of Alaska Anchorage (US)
Corresponding author
Simons, Brenna C.
Venue
Journal of Infectious Diseases
Published
2016-04-07
Volume
214
Issue
2
Pages
273-280
ISSN
  • 0022-1899 (ISSN-L)
  • 1537-6613
OpenAlex
W2359724621
Cited by
101
References
50
Citations by year
2026: 10 · 2025: 10 · 2024: 16 · 2023: 10 · 2022: 16 · 2021: 12 · 2020: 6 · 2019: 7 · 2018: 6 · 2017: 7 · 2016: 1
FWCI
6.56
Type
journal article
Language
en
Open access
Locations
  • The Journal of Infectious Diseases (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • HighWire Press Open Archive (submittedVersion)
Funders
  • CDC (U01 PS001097)
  • National Institute of General Medical Sciences
  • National Institutes of Health
  • NIH (P20GM103395, U261IHS0046)
Topics
  • Health Sciences › Medicine › Epidemiology › Hepatitis B Virus Studies
  • Health Sciences › Medicine › Hepatology › Hepatitis C virus research
  • Health Sciences › Medicine › Emergency Medicine › Intramuscular injections and effects
Keywords
hepatitis B vaccine, hepatitis B virus, cell-mediated immunity, hepatitis B surface antigen, HBV core antigen, NKT cells, cytokine production, miR-155, plasma-derived vaccine
MeSH terms
Adult, Cytological Techniques, Female, Hepatitis B, Hepatitis B Antibodies, Hepatitis B Surface Antigens, Hepatitis B virus, Humans, Immunity, Cellular, Longitudinal Studies, Male, Middle Aged, T-Lymphocytes, Time Factors, Hepatitis B Vaccines, MicroRNAs, Enzyme-Linked Immunospot Assay

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