Quantification and functional analysis of plasmacytoid dendritic cells in patients with chronic hepatitis C virus infection
N Goutagny, C Vieux, E Decullier… - The Journal of …, 2004 - academic.oup.com
N Goutagny, C Vieux, E Decullier, B Ligeoix, A Epstein, C Trépo, P Couzigou, G Inchauspé…
The Journal of infectious diseases, 2004•academic.oup.comAbstract Background. Plasmacytoid dendritic cells (PDCs) are the major producers of
interferon (IFN)-α within peripheral blood mononuclear cells (PBMCs). Methods. We
analyzed whether chronic hepatitis C virus (HCV) infection could be linked to a defective
function or number of PDCs. We evaluated the capacity of PBMCs from 5 cohorts of subjects
to produce IFN-α after viral stimulation. We concomitantly analyzed the frequency of PDCs
and the levels of IFN-α transcripts within the PBMCs from the same cohorts. Results. PBMCs …
interferon (IFN)-α within peripheral blood mononuclear cells (PBMCs). Methods. We
analyzed whether chronic hepatitis C virus (HCV) infection could be linked to a defective
function or number of PDCs. We evaluated the capacity of PBMCs from 5 cohorts of subjects
to produce IFN-α after viral stimulation. We concomitantly analyzed the frequency of PDCs
and the levels of IFN-α transcripts within the PBMCs from the same cohorts. Results. PBMCs …
Abstract
Background. Plasmacytoid dendritic cells (PDCs) are the major producers of interferon (IFN)-α within peripheral blood mononuclear cells (PBMCs).
Methods. We analyzed whether chronic hepatitis C virus (HCV) infection could be linked to a defective function or number of PDCs. We evaluated the capacity of PBMCs from 5 cohorts of subjects to produce IFN-α after viral stimulation. We concomitantly analyzed the frequency of PDCs and the levels of IFN-α transcripts within the PBMCs from the same cohorts.
Results. PBMCs from patients with chronic HCV infection receiving antiviral therapy displayed a reduced capacity to release IFN-α, compared with those from healthy individuals, those from long-term responders to therapy, and those from nontreated patients. This defect was significantly correlated with the percentage of PDCs. In addition, PDCs from patients with chronic HCV infection receiving therapy displayed a reduced intrinsic capacity to produce IFN-α, which could be linked to the level of IFN-α transcripts.
Conclusion. Our observations point to an effect of the therapy on either the survival or the localization of PDCs, rather than a direct detrimental effect due to the viral infection during chronic HCV infection.
Oxford University Press