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Int Immunopharmacol ; 91: 107302, 2021 Feb.
Article in English | MEDLINE | ID: mdl-33395584

ABSTRACT

The treatment for hepatitis Delta virus (HDV) still consists of Pegylated interferon (PEG-IFN) combined with inhibitors of Hepatitis B virus (HBV) replication. In some patients may be occur a virological response, which means a negative HDV RNA 6 months after stopping treatment. In this study it was conducted an in vitro approach with the aim to mimic possible immunological events that are observed in patients responding to PEG-IFN therapy. Jurkat cells (human T lymphocyte cell line) were employed alone or co-cultured with THP-1 (human monocytic cell line) and stimulated with controls and HBV Surface Antigen (HBsAg), Small-Delta Antigen (SHDAg), and HBsAg + SHDAg combined. Twenty-four hours stimulation with SHDAg and/or HBSAg led to a toxic profile in a co-culture condition and cell supernatants were collected for cytokines quantification. PEG-IFN was added and cells were incubated for additional 24 h. Co-cultured cells incubated with the association (SHDAg + PEG-IFN) significantly produced levels of IFN-γ, IL-2 and IL-12. On the other hand, the HBsAg alone was able to inhibit the production of IFN-γ, suggesting that this antigen may hinder the treatment exclusively with PEG-IFN.


Subject(s)
Antiviral Agents/pharmacology , Cytokines/metabolism , Cytotoxicity, Immunologic/drug effects , Hepatitis D/drug therapy , Hepatitis Delta Virus/immunology , Interferons/pharmacology , Polyethylene Glycols/pharmacology , Coculture Techniques , Hepatitis B Surface Antigens/pharmacology , Hepatitis D/immunology , Hepatitis D/metabolism , Hepatitis D/virology , Hepatitis Delta Virus/pathogenicity , Hepatitis delta Antigens/pharmacology , Host-Pathogen Interactions , Humans , Interferon-gamma/metabolism , Interleukin-12/metabolism , Interleukin-2/metabolism , Jurkat Cells , Signal Transduction , THP-1 Cells
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