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Interferon‐β enhancement of human dendritic cell activation
Author(s) -
PhippsYonas Hannah,
Seto Jeremy,
FernandezSesma Ana,
Moran Thomas M.
Publication year - 2008
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.22.2_supplement.498
Subject(s) - interferon , immune system , virus , biology , priming (agriculture) , influenza a virus , dendritic cell , virology , viral replication , context (archaeology) , immunology , microbiology and biotechnology , paleontology , botany , germination
Influenza virus produces a protein, NS1, that inhibits infected cells from releasing type I interferon (IFN) and blocks maturation of conventional dendritic cells (DCs). As a result, influenza virus is a poor activator of both mouse and human DCs in vitro . However, a strong immune response is generated in both species in response to virus infection suggesting that other factors may contribute to the maturation of DC in vivo . It is likely that the environment in which a DC encounters a virus would contain multiple pro‐inflammatory molecules, including type I IFN. Type I IFN is a critical component of viral immune response that initiates an antiviral state in cells, primarily by triggering a broad transcriptional program that interferes with the ability of virus to establish infection in the cell. In this study we have examined the activation profiles of both conventional and plasmacytoid dendritic cells (cDCs and pDCs) in response to an influenza virus infection in the context of a type I IFN‐containing environment. We found that both cDCs and pDCs demonstrate a greater activation response to influenza virus when pre‐exposed to IFN‐β (IFN priming); although, the priming kinetics are different in these two cell types. This strongly suggests that type I IFN functions to, not only reduce viral replication in these immune cells but, promote greater DC activation during viral infections.