The basal activation state of DC subsets correlates with anti-HCV treatment outcome in HCV/HIV co-infected patients

被引:3
作者
Sacchi, Alessandra [1 ]
Agrati, Chiara [1 ,2 ]
D'Offizi, Gianpiero [3 ]
Vlassi, Chrysoula [3 ]
Rozera, Gabriella [2 ]
Abbate, Isabella [2 ]
Capobianchi, Maria Rosaria [2 ]
Martini, Federico [1 ]
机构
[1] IRCCS, Natl Inst Infect Dis Lazzaro Spallanzani, Cellular Immunol Lab, I-00149 Rome, Italy
[2] IRCCS, Natl Inst Infect Dis Lazzaro Spallanzani, Clin Dept, I-00149 Rome, Italy
[3] IRCCS, Natl Inst Infect Dis Lazzaro Spallanzani, Virol Lab, I-00149 Rome, Italy
关键词
HCV; HIV; Dendritic cells; IFN-alpha; CHRONIC HEPATITIS-C; PLASMACYTOID DENDRITIC CELLS; BLOOD MONONUCLEAR-CELLS; VIRUS-INFECTION; HIV-1; INFECTION; IFN-ALPHA; IN-VITRO; T-CELLS; INTERFERON; THERAPY;
D O I
10.1016/j.clim.2010.11.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this work we evaluated plasmacytoid (pDC) and myeloid dendritic (mDC) cells activation before and during anti-HCV treatment in HCV+/HIV+ individuals. HCV+/HIV+ patients received Peg-IFN-alpha 2b subcutaneously for 28 days, followed by oral weight-based ribavirin. DCs activation was evaluated by flow cytometry. Baseline pDC CD80 and CD86 expression was correlated with HIV, but not with HCV viral load. A transient decrease of HIV RNA was found not associated with DC activation. When patients were grouped according to early/sustained virological response (EVR/SVR) to anti-HCV treatment, baseline pDC CD80 and CD86 expression was higher in non-EVR and non-SVR compared to EVR and SVR. Moreover, in responder patients CD80 and CD86 were upregulated by IFN-alpha. Our data suggest a correlation between DCs activation and response to therapy. These findings could be helpful to better understand the mediators of IFN-alpha action in HCV+/HIV+ patients and to explore possible exploitation of this knowledge to improve therapeutic response. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:178 / 186
页数:9
相关论文
共 39 条
[1]   Epidemiology of viral hepatitis and HIV co-infection [J].
Alter, MJ .
JOURNAL OF HEPATOLOGY, 2006, 44 :S6-S9
[2]   Selective impairments in dendritic cell-associated function distinguish hepatitis C virus and HIV infection [J].
Anthony, DD ;
Yonkers, NL ;
Post, AB ;
Asaad, R ;
Heinzel, FP ;
Lederman, MM ;
Lehmann, PV ;
Valdez, H .
JOURNAL OF IMMUNOLOGY, 2004, 172 (08) :4907-4916
[3]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[4]   Impact of alpha interferon and ribavirin on the function of maturing dendritic cells [J].
Barnes, E ;
Salio, M ;
Cerundolo, V ;
Medlin, J ;
Murphy, S ;
Dusheiko, G ;
Klenerman, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (09) :3382-3389
[5]   Influence of plasma viremia on defects in number and immunophenotype of blood dendritic cell subsets in human immunodeficiency virus 1-infected individuals [J].
Barron, MA ;
Blyveis, N ;
Palmer, BE ;
MaWhinney, S ;
Wilson, CC .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 (01) :26-37
[6]   Factors affecting liver fibrosis in human immunodeficiency virus- and hepatitis C virus-coinfected patients: Impact of protease inhibitor therapy [J].
Benhamou, Y ;
Di Martino, V ;
Bochet, M ;
Colombet, G ;
Thibault, V ;
Liou, A ;
Katlama, C ;
Poynard, T .
HEPATOLOGY, 2001, 34 (02) :283-287
[7]   Human CD1b and CD1c isoforms survey different intracellular compartments for the presentation of microbial lipid antigens [J].
Briken, V ;
Jackman, RM ;
Watts, GFM ;
Rogers, RA ;
Porcelli, SA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (02) :281-287
[8]   Dendritic cells generated in the presence of granulocyte-macrophage colony-stimulating factor and IFN-α are potent inducers of HIV-specific CD8 T cells [J].
Carbonneil, C ;
Aouba, A ;
Burgard, M ;
Cardinaud, S ;
Rouzioux, C ;
Langlade-Demoyen, P ;
Weiss, L .
AIDS, 2003, 17 (12) :1731-1740
[9]   Persistent decreases in blood plasmacytoid dendritic cell number and function despite effective highly active antiretroviral therapy and increased blood myeloid dendritic cells in HIV-infected individuals [J].
Chehimi, J ;
Campbell, DE ;
Azzoni, L ;
Bacheller, D ;
Papasavvas, E ;
Jerandi, G ;
Mounzer, K ;
Kostman, J ;
Trinchieri, G ;
Montaner, LJ .
JOURNAL OF IMMUNOLOGY, 2002, 168 (09) :4796-4801
[10]   Hepatic gene expression discriminates responders and nonresponders in treatment of chronic hepatitis C viral infection [J].
Chen, LM ;
Borozan, I ;
Feld, J ;
Sun, J ;
Tannis, LL ;
Coltescu, C ;
Heathcote, J ;
Edwards, AM ;
McGilvray, ID .
GASTROENTEROLOGY, 2005, 128 (05) :1437-1444