Journal of Hepatology
Volume 42, Issue 1 , Pages 61-67 , January 2005

Comparable functions of plasmacytoid and monocyte-derived dendritic cells in chronic hepatitis C patients and healthy donors

  • Diego Piccioli

      Affiliations

    • Immunology and Virology Department, Chiron Vaccines Research Center, via Fiorentina 1, 53100 Siena, Italy
  • ,
  • Simona Tavarini

      Affiliations

    • Immunology and Virology Department, Chiron Vaccines Research Center, via Fiorentina 1, 53100 Siena, Italy
  • ,
  • Sandra Nuti

      Affiliations

    • Immunology and Virology Department, Chiron Vaccines Research Center, via Fiorentina 1, 53100 Siena, Italy
  • ,
  • Piero Colombatto

      Affiliations

    • Gastroenterology and Hepatology Unit, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy
  • ,
  • Maurizia Brunetto

      Affiliations

    • Gastroenterology and Hepatology Unit, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy
  • ,
  • Ferruccio Bonino

      Affiliations

    • Gastroenterology and Hepatology Unit, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy
  • ,
  • Pietro Ciccorossi

      Affiliations

    • Gastroenterology and Hepatology Unit, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy
  • ,
  • Francesca Zorat

      Affiliations

    • Institute of Internal Medicine, School of Medicine, University of Trieste, Trieste, Italy
  • ,
  • Gabriele Pozzato

      Affiliations

    • Institute of Internal Medicine, School of Medicine, University of Trieste, Trieste, Italy
  • ,
  • Consuelo Comar

      Affiliations

    • Institute of Internal Medicine, School of Medicine, University of Trieste, Trieste, Italy
  • ,
  • Sergio Abrignani

      Affiliations

    • Immunology and Virology Department, Chiron Vaccines Research Center, via Fiorentina 1, 53100 Siena, Italy
    • Corresponding Author InformationCorresponding author. Tel.: +39 577 243032; fax: +39 577 243564.
  • ,
  • Andreas Wack

      Affiliations

    • Immunology and Virology Department, Chiron Vaccines Research Center, via Fiorentina 1, 53100 Siena, Italy

Received 20 July 2004 ,Revised 14 September 2004 ,Accepted 21 September 2004.

  • Image Result

    Chronic HCV patient and healthy donor Mo-DCs respond similarly to LPS by up-regulation of maturation markers. A, average of MFI±SD of B7.2 (CD86), CD83, HLA-DR maturation markers with (white bar) or w

    Chronic HCV patient and healthy donor Mo-DCs respond similarly to LPS by up-regulation of maturation markers. A, average of MFI±SD of B7.2 (CD86), CD83, HLA-DR maturation markers with (white bar) or without (black bar) LPS stimulation in HCV patient and healthy donor Mo-DCs. B, comparison, as representative example, of B7.2 (CD86), CD83, HLA-DR fluorescence histograms before (thin line) and after (bold line) LPS stimulation, between a healthy donor and a HCV patient Mo-DCs. Cells from 10 different healthy donors and 10 HCV patients were assessed. LPS was used at 100ng/ml.

  • Image Result
    Chronic HCV patient and healthy donor Mo-DCs have comparable allostimulatory capacity. (A) Average of stimulation indices (SIs)±SD in MLR at the Stimulator/Responder ratio of 1/20, using as stimulator

    Chronic HCV patient and healthy donor Mo-DCs have comparable allostimulatory capacity. (A) Average of stimulation indices (SIs)±SD in MLR at the Stimulator/Responder ratio of 1/20, using as stimulator cells immature Mo-DCs from healthy donors (white bar) or from HCV chronic patients (black bar). Allogeneic PBMCs are used as responder cells. 10 different healthy donors and HCV patients were analyzed. (B) Representative example of SIs at different Stimulator/Responder ratios, in two MLRs performed using healthy donor (white circle) or HCV patient (black circle) Mo-DCs as stimulator cells. (C) Thymidine incorporation in two MLRs with donor (white square) and HCV patient (black square) Mo-DCs as stimulator cells. SI is the ratio of cpm between samples with stimulator plus responder cells and samples with responder cells alone.

  • Image Result
    Chronic HCV patient and healthy donor Mo-DCs produce TNF-α with similar efficiency. TNF-α quantified by sandwich ELISA in culture supernatant of healthy donor and chronic HCV patient Mo-DCs stimulated

    Chronic HCV patient and healthy donor Mo-DCs produce TNF-α with similar efficiency. TNF-α quantified by sandwich ELISA in culture supernatant of healthy donor and chronic HCV patient Mo-DCs stimulated with LPS at 100ng/ml. We used 10 different healthy donors and HCV patients. P>0.3 (Student's t-test).

  • Image Result
    pDCs from chronic HCV patients and healthy donors show comparable TNF-α and IFN-α production. (A) Average±SD of percentage of TNF-α and IFN-α positive pDCs, as revealed by intracellular staining, in 2

    pDCs from chronic HCV patients and healthy donors show comparable TNF-α and IFN-α production. (A) Average±SD of percentage of TNF-α and IFN-α positive pDCs, as revealed by intracellular staining, in 24 healthy donors (white bar) and 10 HCV chronic patients (black bar). (B) and (C) Dot plots of BDCA-2+ gated pDCs stained for TNF-α and IFN-α from a healthy donor (B) or a chronic HCV patient (C). PBMCs were incubated overnight with CpG 2216 at 10μg/ml. Brefeldin was added after 4–6h of stimulation at final concentration of 2μg/ml.

PII: S0168-8278(04)00454-4

doi: 10.1016/j.jhep.2004.09.014

Journal of Hepatology
Volume 42, Issue 1 , Pages 61-67 , January 2005