Abstract
1. Hyper-induction of cytokines and chemokines was found in human blood macrophages infected with the avian influenza H5N1 and H9N2/G1 viruses, as compared to those infected with human influenza H1N1 virus. 2. IRF3 played a significant role in the hyperinduction of cytokines including IFN-β, IFN-λ1,IFN-α subtypes, MCP-1, and TNF-α, and also played a part in subsequent cytokine-induced cell signalling cascades. 3. Compared with H1N1 viruses, avian influenza viruses including H5N1/97 and its precursors triggered a caspase-mediated but delayed apoptotic response in human macrophages. 4. Therapies that can minimise immunopathology-associated dysregulation of innate immunity without impairing effective host defence may be valuable adjuncts to antiviral therapy.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Apoptosis*
-
Caspase 3 / metabolism
-
Cells, Cultured
-
Cytokines / biosynthesis
-
Cytokines / genetics*
-
Gene Expression Regulation
-
Humans
-
Influenza A Virus, H1N1 Subtype
-
Influenza A Virus, H5N1 Subtype*
-
Influenza, Human / metabolism*
-
Interferon Regulatory Factor-3 / genetics
-
Interferon Regulatory Factor-3 / metabolism*
-
Interferon-beta / biosynthesis
-
Interferon-beta / genetics
-
Interferons
-
Interleukins / biosynthesis
-
Interleukins / genetics
-
Macrophages / enzymology
-
Macrophages / metabolism*
-
Macrophages / virology
-
Poly(ADP-ribose) Polymerases / metabolism
-
RNA, Messenger / metabolism*
-
RNA, Small Interfering
-
Transcription Factors / metabolism
-
Tumor Necrosis Factor-alpha / biosynthesis
-
Tumor Necrosis Factor-alpha / genetics
-
Up-Regulation / genetics
Substances
-
Cytokines
-
IFNL1 protein, human
-
IRF3 protein, human
-
Interferon Regulatory Factor-3
-
Interleukins
-
RNA, Messenger
-
RNA, Small Interfering
-
Transcription Factors
-
Tumor Necrosis Factor-alpha
-
Interferon-beta
-
Interferons
-
Poly(ADP-ribose) Polymerases
-
Caspase 3