AI Article Synopsis

  • The WHO recommends hepatitis B vaccination from infancy due to its widespread presence and health risks, but existing vaccines aren’t 100% effective, leaving some individuals unprotected.
  • Using mRNA-sequencing, the study assessed immune responses after the Engerix-B vaccine, finding differences in gene expression before vaccination that correlated with antibody responses after two doses.
  • Non-responders showed an already activated immune state before vaccination and a delayed immune response afterward, suggesting that pre-existing immune conditions can affect the efficacy of hepatitis B vaccination.

Article Abstract

Introduction: As the hepatitis B virus is widely spread and responsible for considerable morbidity and mortality, WHO recommends vaccination from infancy to reduce acute infection and chronic carriers. However, current subunit vaccines are not 100% efficacious and leave 5-10% of recipients unprotected.

Methods: To evaluate immune responses after Engerix-B vaccination, we determined, using mRNA-sequencing, whole blood early gene expression signatures before, at day 3 and day 7 after the first dose and correlated this with the resulting antibody titer after two vaccine doses.

Results: Our results indicate that immune related genes are differentially expressed in responders mostly at day 3 and in non-responders mostly at day 7. The most remarkable difference between responders and non-responders were the differentially expressed genes before vaccination. The granulin precursor gene (GRN) was significantly downregulated in responders while upregulated in non-responders at day 0. Furthermore, absolute granulocytes numbers were significantly higher in non-responders at day 0.

Conclusion: The non-responders already showed an activated state of the immune system before vaccination. Furthermore, after vaccination, they exhibited a delayed and partial immune response in comparison to the responders. Our data may indicate that the baseline and untriggered immune system can influence the response upon hepatitis B vaccination.

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Source
http://dx.doi.org/10.1016/j.vaccine.2018.09.001DOI Listing

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