TY - JOUR
T1 - The immune responsiveness in hepatitis C virus infected patients
T2 - Effects of interferon-alfa/ribavirin combined treatment on the lymphocyte response with special reference to B cells
AU - Amati, Luigi
AU - Cozzolongo, R.
AU - Manghisi, O. G.
AU - Cuppone, R.
AU - Pellegrino, N. M.
AU - Caccavo, D.
AU - Jirillo, E.
PY - 2004
Y1 - 2004
N2 - Previous data demonstrated that an elevated percentage of hepatitis C virus (HCV) infected patients are endotoxemic. Endotoxemic patients are poor responders to the interferon (IFN)- α/ribavirin (RIB) treatment and exhibit lower serum levels of IFN-γ and interleukin (IL)-10 than the responder counterpart. Here we provide evidence that in endotoxemic HCV+ patients absolute numbers of CD19+ cells (B cells) are higher than those observed in the non-endotoxemic counterpart at the end of the combined treatment. Moreover, anti lactoferrin (LF) antibodies are more elevated in non-responder HCV+ patients than in the responders. In turn, these autoantibodies may affect the antiviral activity of LF, on the one hand, and, on the other hand abrogate the LF binding to lipopolysaccharides (LPS). Such an interaction hampers the binding of LPS to LPS binding protein, thus inhibiting LPS fixation to CD14+ cells and, ultimately, leading to a decreased release of proinflammatory cytokines.
AB - Previous data demonstrated that an elevated percentage of hepatitis C virus (HCV) infected patients are endotoxemic. Endotoxemic patients are poor responders to the interferon (IFN)- α/ribavirin (RIB) treatment and exhibit lower serum levels of IFN-γ and interleukin (IL)-10 than the responder counterpart. Here we provide evidence that in endotoxemic HCV+ patients absolute numbers of CD19+ cells (B cells) are higher than those observed in the non-endotoxemic counterpart at the end of the combined treatment. Moreover, anti lactoferrin (LF) antibodies are more elevated in non-responder HCV+ patients than in the responders. In turn, these autoantibodies may affect the antiviral activity of LF, on the one hand, and, on the other hand abrogate the LF binding to lipopolysaccharides (LPS). Such an interaction hampers the binding of LPS to LPS binding protein, thus inhibiting LPS fixation to CD14+ cells and, ultimately, leading to a decreased release of proinflammatory cytokines.
KW - B lymphocytes
KW - Endotoxins
KW - Hepatitis C virus
KW - Interferon-α
KW - Ribavirin
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U2 - 10.2174/1381612043384231
DO - 10.2174/1381612043384231
M3 - Article
C2 - 15279548
AN - SCOPUS:3042555478
SN - 1381-6128
VL - 10
SP - 2093
EP - 2100
JO - Current Pharmaceutical Design
JF - Current Pharmaceutical Design
IS - 17
ER -