TY - JOUR
T1 - Hepatitis C virus NS4 protein impairs the Th1 polarization of immature dendritic cells
AU - Takaki, A.
AU - Tatsukawa, M.
AU - Iwasaki, Y.
AU - Koike, K.
AU - Noguchi, Y.
AU - Shiraha, H.
AU - Sakaguchi, K.
AU - Nakayama, E.
AU - Yamamoto, K.
PY - 2010/8
Y1 - 2010/8
N2 - Dendritic cells (DCs) in chronic hepatitis C patients display impaired function, although the details remain unclear. To investigate the hepatitis C virus (HCV) protein that has the most impact on DC function, we compared five recombinant proteins and seven HCV protein genes in modulating DC phenotype and function. Immature DCs (iDCs) were established from healthy donor peripheral blood monocytes with granulocyte-macrophage colony stimulating factor (GM-CSF) and IL-4. Lipopolysaccharide was used to establish mature DCs (mDCs). Cells were then pulsed with HCV recombinant proteins or transfected with HCV plasmids and subsequently assayed for cell surface marker expression by flow cytometry. For cytokine and proliferative T-cell response analysis, DCs were cultured with autologous CD4 T cells and tuberculin purified protein derivative (PPD). Mean fluorescent intensity of CD86 was reduced in HCV protein-pulsed iDCs. Proliferative T-cell responses and Th1 cytokine concentrations were reduced with HCV nonstructural proteins (NS), particularly with HCV NS4. HCV nonstructural proteins, particularly NS4, change the iDC phenotype and reduce antigen-specific T-cell stimulatory function with Th1 cytokine reductions.
AB - Dendritic cells (DCs) in chronic hepatitis C patients display impaired function, although the details remain unclear. To investigate the hepatitis C virus (HCV) protein that has the most impact on DC function, we compared five recombinant proteins and seven HCV protein genes in modulating DC phenotype and function. Immature DCs (iDCs) were established from healthy donor peripheral blood monocytes with granulocyte-macrophage colony stimulating factor (GM-CSF) and IL-4. Lipopolysaccharide was used to establish mature DCs (mDCs). Cells were then pulsed with HCV recombinant proteins or transfected with HCV plasmids and subsequently assayed for cell surface marker expression by flow cytometry. For cytokine and proliferative T-cell response analysis, DCs were cultured with autologous CD4 T cells and tuberculin purified protein derivative (PPD). Mean fluorescent intensity of CD86 was reduced in HCV protein-pulsed iDCs. Proliferative T-cell responses and Th1 cytokine concentrations were reduced with HCV nonstructural proteins (NS), particularly with HCV NS4. HCV nonstructural proteins, particularly NS4, change the iDC phenotype and reduce antigen-specific T-cell stimulatory function with Th1 cytokine reductions.
KW - T cell
KW - dendritic cell
KW - hepatitis C virus
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UR - http://www.scopus.com/inward/citedby.url?scp=77954508223&partnerID=8YFLogxK
U2 - 10.1111/j.1365-2893.2009.01213.x
DO - 10.1111/j.1365-2893.2009.01213.x
M3 - Article
C2 - 19804500
AN - SCOPUS:77954508223
SN - 1352-0504
VL - 17
SP - 555
EP - 562
JO - Journal of Viral Hepatitis
JF - Journal of Viral Hepatitis
IS - 8
ER -