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
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