TY - JOUR
T1 - Transcriptomic Analysis of Livers of Inactive Carriers of Hepatitis B Virus with Distinct Expression of Hepatitis B Surface Antigen
AU - Rico Montanari, Noe
AU - Ramirez, Ricardo
AU - Van Buuren, Nick
AU - van den Bosch, Thierry P.P.
AU - Doukas, Michail
AU - Debes, Jose D.
AU - Feierbach, Becket
AU - Boonstra, Andre
N1 - Publisher Copyright:
© 2021 The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.
PY - 2022/3/15
Y1 - 2022/3/15
N2 - Inactive carrier phases in chronic hepatitis B virus (HBV) infection present minimal liver disease and HBV replication activity suggesting partial immune reconstitution, although the mechanisms responsible remain elusive. Moreover, hepatitis B surface antigen (HBsAg) production-hypothesized to modulate the immune response-is unaltered. In the current study, we assessed the intrahepatic transcriptome in inactive carriers of HBV versus healthy liver donors, including in the context of diverse HBsAg levels (serum and liver), to better understand the phenomenon of immune control. We found a deregulated liver transcriptome in inactive carriers compared with healthy controls, despite normal liver function. Moreover, diverse HBsAg levels have minimal impact on the liver transcriptome in inactive carriers, although gene correlation analysis revealed that leukocyte activation, recruitment, and innate responses genes were correlated with liver HBsAg levels. These findings provide more insight into the mechanisms underlying anti-HBV strategies currently under development, aimed at interfering with HBsAg production or inducing a state of immune control.
AB - Inactive carrier phases in chronic hepatitis B virus (HBV) infection present minimal liver disease and HBV replication activity suggesting partial immune reconstitution, although the mechanisms responsible remain elusive. Moreover, hepatitis B surface antigen (HBsAg) production-hypothesized to modulate the immune response-is unaltered. In the current study, we assessed the intrahepatic transcriptome in inactive carriers of HBV versus healthy liver donors, including in the context of diverse HBsAg levels (serum and liver), to better understand the phenomenon of immune control. We found a deregulated liver transcriptome in inactive carriers compared with healthy controls, despite normal liver function. Moreover, diverse HBsAg levels have minimal impact on the liver transcriptome in inactive carriers, although gene correlation analysis revealed that leukocyte activation, recruitment, and innate responses genes were correlated with liver HBsAg levels. These findings provide more insight into the mechanisms underlying anti-HBV strategies currently under development, aimed at interfering with HBsAg production or inducing a state of immune control.
KW - HBsAg
KW - hepatitis B
KW - intrahepatic transcriptome
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U2 - 10.1093/infdis/jiab381
DO - 10.1093/infdis/jiab381
M3 - Article
C2 - 34279652
AN - SCOPUS:85126490348
SN - 0022-1899
VL - 225
SP - 1081
EP - 1090
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 6
ER -