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Journal Summaries in Gastroenterology
HBV vaccination and HBV infection induces HBV-specific natural killer cell memory
Gut — Wijaya RS2, Read SA, Truong NR, et al. | April 01, 2020
The identification of antigen-specific memory natural killer cells (mNKs) in mice and non-human primates has challenged the view that vaccination against hepatitis B virus (HBV) confers protection from subsequent infection through immunological memory that is traditionally considered the domain of the adaptive immune system. Researchers examined humans for the existence of HBV-specific mNKs after vaccination and in chronic HBV infection. Flow cytometry and ELISA were used to evaluate NK cell responses following challenge with HBV antigens in HBV vaccinated, non-vaccinated and chronic HBV-infected individuals. They observed higher cytotoxic and proliferative responses against autologous hepatitis B surface antigen (HBsAg)-pulsed monocyte-derived dendritic cells (moDCs) in NK cells from vaccinated subjects vs unvaccinated subjects. Moreover, significantly higher NK cell lysis of HBsAg-pulsed moDCs was observed relative to that of hepatitis B core antigen (HBcAg)-pulsed moDCs (non-vaccine antigen) or tumor necrosis factor α-activated moDCs in a NKG2D-dependent manner. Further, greater degranulation against HBcAg-pulsed moDCs was observed in mNKs from chronic hepatitis B patients vs unvaccinated or vaccinated patients. Notably, there was a negative correlation of mNK activity with HBV DNA levels. Data suggest the existence of a mature mNKs following HBV antigen exposure either through vaccination or infection. For developing novel treatments targeting HBV in chronic infection, harnessing these antigen specific, functionally active mNKs provides an opportunity. |
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