Immunomodulation and RNA interference alter hepatitis B virus–specific CD8 T‐cell recognition of infected HepG2‐NTCP
Autor: | Adrian Kuipery, Aman Mehrotra, Harry L.A. Janssen, Jordan J. Feld, Adam J. Gehring, Juan Diego Sanchez Vasquez |
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Rok vydání: | 2022 |
Předmět: |
Hepatitis B virus
HBsAg T cell Antigen presentation CD8-Positive T-Lymphocytes Biology medicine.disease_cause Immunomodulation Hepatitis B Chronic Immune system Antigen medicine Humans Cytotoxic T cell Tenofovir Hepatology virus diseases Virology digestive system diseases HBcAg medicine.anatomical_structure Toll-Like Receptor 7 Toll-Like Receptor 8 Culture Media Conditioned Interferon Type I RNA Interference |
Zdroj: | Hepatology. 75:1539-1550 |
ISSN: | 1527-3350 0270-9139 |
Popis: | BACKGROUND & AIMS CD8 T cells are essential in controlling Hepatitis B virus (HBV) infection. Viral control is dependent on efficient recognition of HBV-infected hepatocytes by CD8 T cells, which can induce direct lysis of infected hepatocytes. In addition, CD8 T cells produce IFN-γ, which mediates non-cytopathic viral clearance. Innate immunomodulators and HBV-targeted RNA interference (RNAi) are being developed to treat chronic hepatitis B, but may modify HBV antigen presentation and impact CD8 T cell recognition, in addition to their primary mechanisms of action. APPROACH & RESULTS HBV infected HepG2-NTCP were treated with tenofovir disoproxil fumarate (TDF), Toll-like receptor (TLR) 7/8 agonists, TLR7/8 conditioned media (CM) collected from immune cells, or RNAi using short-interfering RNAs (siRNAs). The effect of these treatments on antigen presentation was measured through co-culture with CD8 T cells recognizing HLA-A0201 restricted epitopes, HBc18-27 or HBs183-191. Cytokine profiles of TLR7/8 CM was measured using cytometric bead array. TDF reduced viral replication, but not CD8 T cell recognition of infected cells. Direct exposure of infected HepG2-NTCP to TLR7/8 agonists had no impact on T cell recognition. Exposure of infected HepG2-NTCP to TLR7/8 CM enhanced HBV-specific CD8 T cell recognition through type 1 interferon (IFN) and IFN-γ dependent mechanisms. RNAi rapidly suppressed HBV DNA, HBV Core antigen (HBcAg), and HBV S antigen (HBsAg) expression, impairing recognition by HBV-specific CD8 T cells. CONCLUSIONS Immunomodulation, and RNAi, but not nucleos(t)ide analogues, alter recognition of infected HepG2-NTCP by HBV-specific CD8 T cells. Understanding these changes will inform combination treatments for CHB. |
Databáze: | OpenAIRE |
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