Immune function of plasmacytoid dendritic cells, natural killer cells, and their crosstalk in HBV infection

被引:27
作者
Golsaz-Shirazi, Forough [1 ]
Amiri, Mohammad Mehdi [1 ]
Shokri, Fazel [1 ,2 ]
机构
[1] Univ Tehran Med Sci, Sch Publ Hlth, Dept Immunol, Tehran, Iran
[2] Avicenna Res Inst, Monoclonal Antibody Res Ctr, Tehran, Iran
基金
美国国家科学基金会;
关键词
HBV infection; natural killer cells; plasmacytoid dendritic cells; HEPATITIS-B-VIRUS; NK CELLS; IMPAIRED FUNCTION; HUMAN LIVER; IFN-ALPHA; INNATE; ACTIVATION; RESPONSES; ANTIGEN; BLOOD;
D O I
10.1002/rmv.2007
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Chronic hepatitis B virus infection is a major health problem, with over 245 million chronic carriers worldwide. This persistent infection is thought to be associated with inefficient innate and adaptive immune responses. Natural killer cells (NK cells) and plasmacytoid dendritic cells (pDCs) are the major innate immune cells which respond to viral infection at the early phase and are considered major components of the antiviral immune response. In this review, we summarize recent findings regarding the role of NK cells, pDCs, and their cross-talk in HBV infection and its chronicity. Although the data regarding the biological function of pDCs and NK cells in HBV infection is still controversial, many studies show that in chronic HBV infection, the cytotoxicity of NK cells is retained, while their capacity to secrete cytokines is strongly impaired. In addition, interferon-alpha production by pDCs is impaired during chronic HBV infection, and the virus interferes with pDC-NK cell interaction.
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页数:15
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共 86 条
[1]  
Arima S, 2003, INT J MOL MED, V11, P169
[2]   Reduction in the circulating pDC1/pDC2 ratio and impaired function of ex vivo-generated DC1 in chronic hepatitis B infection [J].
Beckebaum, S ;
Cicinnati, VR ;
Dworacki, G ;
Müller-Berghaus, J ;
Stolz, D ;
Harnaha, J ;
Whiteside, TL ;
Thomson, AW ;
Lu, L ;
Fung, JJ ;
Bonham, CA .
CLINICAL IMMUNOLOGY, 2002, 104 (02) :138-150
[3]   Activation and function of natural killer cell responses during viral infections [J].
Biron, CA .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) :24-34
[4]  
Biron CA, 2017, COLD SPRING HARB PER
[5]   Characterization of hepatitis B virus (HBV)-specific T-cell dysfunction in chronic HBV infection [J].
Boni, Carolina ;
Fisicaro, Paola ;
Valdatta, Caterina ;
Amadei, Barbara ;
Di Vincenzo, Paola ;
Giuberti, Tiziana ;
Laccabue, Diletta ;
Zerbini, Alessandro ;
Cavalli, Albertina ;
Missale, Gabriele ;
Bertoletti, Antonio ;
Ferrari, Carlo .
JOURNAL OF VIROLOGY, 2007, 81 (08) :4215-4225
[6]   Natural Killer Cell Phenotype Modulation and Natural Killer/T-Cell Interplay in Nucleos(t)ide Analogue-Treated Hepatitis e Antigen-Negative Patients With Chronic Hepatitis B [J].
Boni, Carolina ;
Lampertico, Pietro ;
Talamona, Lavinia ;
Giuberti, Tiziana ;
Invernizzi, Federica ;
Barili, Valeria ;
Fisicaro, Paola ;
Rossi, Marzia ;
Cavallo, Maria Cristina ;
Vecchi, Andrea ;
Pedrazzi, Giuseppe ;
Alfieri, Arianna ;
Colombo, Massimo ;
Missale, Gabriele ;
Ferrari, Carlo .
HEPATOLOGY, 2015, 62 (06) :1697-1709
[7]   Fine characterization of intrahepatic NK cells expressing natural killer receptors in chronic hepatitis B and C [J].
Bonorino, Paula ;
Ramzan, Muhammad ;
Camous, Xavier ;
Dufeu-Duchesne, Tania ;
Thelu, Marie-Ange ;
Sturm, Nathalie ;
Dariz, Aurelie ;
Guillermet, Christiane ;
Pernollet, Martine ;
Zarski, Jean-Pierre ;
Marche, Patrice N. ;
Leroy, Vincent ;
Jouvin-Marche, Evelyne .
JOURNAL OF HEPATOLOGY, 2009, 51 (03) :458-467
[8]   The phenotype of hepatitis B virus-specific T cells differ in the liver and blood in chronic hepatitis B virus infection [J].
Chang, J. Judy ;
Thompson, Alexander J. V. ;
Visvanathan, Kumar ;
Kent, Stephen J. ;
Cameron, Paul U. ;
Wightman, Fiona ;
Desmond, Paul ;
Locarnini, Stephen A. ;
Lewin, Sharon R. .
HEPATOLOGY, 2007, 46 (05) :1332-1340
[9]  
Chen YY, 2006, CELL MOL IMMUNOL, V3, P373
[10]   Pathogenesis of hepatitis B virus infection [J].
Chisari, F. V. ;
Isogawa, M. ;
Wieland, S. F. .
PATHOLOGIE BIOLOGIE, 2010, 58 (04) :258-266