Plasmacytoid dendritic cells induce efficient stimulation of antiviral immunity in the context of chronic hepatitis B virus infection

被引:40
作者
Martinet, Jeremie [1 ,2 ,3 ,5 ]
Leroy, Vincent [2 ,3 ,4 ]
Dufeu-Duchesne, Tania [2 ,3 ,4 ]
Larrat, Sylvie [6 ]
Richard, Marie-Jeanne [2 ,3 ,5 ]
Zoulim, Fabien [7 ]
Plumas, Joel [1 ,2 ,3 ,8 ]
Aspord, Caroline [1 ,2 ,3 ]
机构
[1] EFS Rhone Alpes, R&D Lab, F-38701 La Tronche, France
[2] Univ Grenoble 1, Grenoble, France
[3] INSERM, Immunobiol & Immunotherapy Canc U823, La Tronche, France
[4] Michallon Hosp, CHU Grenoble, CNRS, Hepatogastroenterol Unit,UJF,EMBL, Grenoble, France
[5] Michallon Hosp, CHU Grenoble, CNRS, Dept Cancerol & Biotherapy,UJF,EMBL, Grenoble, France
[6] Michallon Hosp, CHU Grenoble, CNRS, Virol Lab,UMI 3265,UJF,EMBL, Grenoble, France
[7] INSERM, Mol Pathobiol & New Treatments Viral Hepatitis U8, F-69008 Lyon, France
[8] UCL, Inst Canc, London, England
关键词
CD8(+) T-CELLS; LYMPHOCYTE EPITOPES; ANTIGEN; RESPONSES; VACCINE; HBV; IMMUNOBIOLOGY; RESOLUTION; PROTEINS; HUMANS;
D O I
10.1002/hep.25879
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The immune control of hepatitis B virus (HBV) infection is essential for viral clearance. Therefore, restoring functional antiHBV immunity is a promising immunotherapeutic approach to treatment of chronic infection. Plasmacytoid dendritic cells (pDCs) play a crucial role in triggering antiviral immunity through their ability to capture and process viral antigens and subsequently induce adaptive immune responses. We investigated the potential of pDCs to trigger antiviral cellular immunity against HBV. We used a human leukocyte antigen A (HLAA)*0201(+) pDC line loaded with HLAA*0201-restricted peptides derived from hepatitis B core/hepatitis B surface (HBc/HBs) antigens to amplify specific CD8 T cells ex vivo from chronic HBV patients and established a Hepato-HuPBL mouse model to address the therapeutic potential of the strategy in vivo. Stimulation of PBMCs or liver-infiltrating lymphocytes from HLAA*0201(+) chronic HBV patients by HBc peptide-loaded pDCs elicited up to 23.1% and 76.1% HBV-specific CD8 T cells in 45.8% of cases. The specific T cells from the responder group secreted interferon-gamma, expressed CD107 upon restimulation, and efficiently lysed HBV antigen-expressing hepatocytes. Circulating hepatitis B e antigen (HBeAg) was found to distinguish the group of patients not responding to the pDC stimulation. The therapeutic efficacy of the pDC vaccine was evaluated in immunodeficient NOD-SCID beta(2)m(-/-) mice reconstituted with HBV patients' PBMCs and xenotransplanted with human HBV-transfected hepatocytes. Vaccination of HepatoHuPBL mice with the HBc/HBs peptideloaded pDCs elicited HBV-specific T cells able to specifically lyse the transfected hepatocytes and reduce the systemic viral load. Conclusion: pDCs loaded with HBVderived peptides can elicit functional virus-specific T cells. HBeAg appears to be critical in determining the outcome of immunotherapies in chronic HBV patients. A pDC-based immunotherapeutic approach could be of interest in attempts to restore functional antiviral immunity, which is critical for the control of the virus in chronic HBV patients. (HEPATOLOGY 2012;56:17061718)
引用
收藏
页码:1706 / 1718
页数:13
相关论文
共 40 条
[1]   Induction of Antiviral Cytotoxic T Cells by Plasmacytoid Dendritic Cells for Adoptive Immunotherapy of Posttransplant Diseases [J].
Aspord, C. ;
Laurin, D. ;
Richard, M. -J. ;
Vie, H. ;
Chaperot, L. ;
Plumas, J. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2011, 11 (12) :2613-2626
[2]   A Novel Cancer Vaccine Strategy Based on HLA-A*0201 Matched Allogeneic Plasmacytoid Dendritic Cells [J].
Aspord, Caroline ;
Charles, Julie ;
Leccia, Marie-Therese ;
Laurin, David ;
Richard, Marie-Jeanne ;
Chaperot, Laurence ;
Plumas, Joel .
PLOS ONE, 2010, 5 (05)
[3]   Plasmacytoid dendritic cells - virus experts of innate immunity [J].
Barchet, W ;
Cella, M ;
Colonna, M .
SEMINARS IN IMMUNOLOGY, 2005, 17 (04) :253-261
[4]   CYTOTOXIC T-LYMPHOCYTE RESPONSE TO A WILD-TYPE HEPATITIS-B VIRUS EPITOPE IN PATIENTS CHRONICALLY INFECTED BY VARIANT VIRUSES CARRYING SUBSTITUTIONS WITHIN THE EPITOPE [J].
BERTOLETTI, A ;
COSTANZO, A ;
CHISARI, FV ;
LEVRERO, M ;
ARTINI, M ;
SETTE, A ;
PENNA, A ;
GIUBERTI, T ;
FIACCADORI, F ;
FERRARI, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (03) :933-943
[5]   T cells redirected against hepatitis B virus surface proteins eliminate infected hepatocytes [J].
Bohne, Felix ;
Chmielewski, Markus ;
Ebert, Gregor ;
Wiegmann, Katja ;
Kuerschner, Timo ;
Schulze, Andreas ;
Urban, Stephan ;
Kroenke, Martin ;
Abken, Hinrich ;
Protzer, Ulrike .
GASTROENTEROLOGY, 2008, 134 (01) :239-247
[6]   Transient restoration of anti-viral T cell responses induced by lamivudine therapy in chronic hepatitis B [J].
Boni, C ;
Penna, A ;
Bertoletti, A ;
Lamonaca, V ;
Rapti, I ;
Missale, G ;
Pilli, M ;
Urbani, S ;
Cavalli, A ;
Cerioni, S ;
Panebianco, R ;
Jenkins, J ;
Ferrari, C .
JOURNAL OF HEPATOLOGY, 2003, 39 (04) :595-605
[7]   Virus or TLR agonists induce TRAIL-mediated cytotoxic activity of plasmacytoid dendritic cells [J].
Chaperot, L ;
Blum, A ;
Manches, O ;
Lui, G ;
Angel, J ;
Molens, JP ;
Plumas, J .
JOURNAL OF IMMUNOLOGY, 2006, 176 (01) :248-255
[8]   A function of the hepatitis B virus precore protein is to regulate the immune response to the core antigen [J].
Chen, MT ;
Billaud, JN ;
Sällberg, M ;
Guidotti, LG ;
Chisari, FV ;
Jones, J ;
Hughes, J ;
Milich, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (41) :14913-14918
[9]   HBcAg-pulsed dendritic cell vaccine induces Th1 polarization and production of hepatitis B virus-specific cytotoxic T lymphocytes [J].
Chen, Weiwei ;
Shi, Ming ;
Shi, Feng ;
Mao, Yuanli ;
Tang, Zirong ;
Zhang, Bin ;
Zhang, Hui ;
Chen, Liangen ;
Chen, Liming ;
Xin, Shaojie ;
Wang, Fu-sheng .
HEPATOLOGY RESEARCH, 2009, 39 (04) :355-365
[10]  
Chisari FV, 1996, CURR TOP MICROBIOL, V206, P149