Strategies to overcome HBV-specific T cell exhaustion: checkpoint inhibitors and metabolic re-programming

被引:35
作者
Fisicaro, Paola [1 ]
Boni, Carolina [1 ]
Barili, Valeria [1 ]
Laccabue, Diletta [1 ]
Ferrari, Carlo [1 ,2 ]
机构
[1] Azienda Osped Univ Parma, Unit Infect Dis & Hepatol, Lab Viral Immunopathol, Parma, Italy
[2] Univ Parma, Dept Med & Surg, Parma, Italy
关键词
HEPATITIS-B; RECEPTOR PD-1; EXPRESSION; RESPONSES; BLOCKADE; DEATH-1; DIFFERENTIATION; REQUIREMENTS; DYSFUNCTION; ACTIVATION;
D O I
10.1016/j.coviro.2018.01.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
HBV-specific T cells play a key role in antiviral protection and failure to control HBV is associated with severely dysfunctional T cell responses. Therefore, functional T cell reconstitution represents a potential way to treat chronically infected patients. The growing understanding of the dysregulated transcriptional/epigenetic and metabolic programs underlying T cell exhaustion allows to envisage functional T cell reconstitution strategies based on the combined/sequential use of compounds able to induce decline of antigen load, checkpoint modulation, metabolic and epigenetic reprogramming with possible boosting of functionally restored responses by specific vaccines.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 74 条
[1]   Impaired NFAT nuclear translocation results in split exhaustion of virus-specific CD8+ T cell functions during chronic viral infection [J].
Agnellini, Paola ;
Wolint, Petra ;
Rehr, Manuela ;
Cahenzli, Julia ;
Karrer, Urs ;
Oxenius, Annette .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (11) :4565-4570
[2]  
[Anonymous], J INTERN MED
[3]   Costimulatory and Coinhibitory Receptor Pathways in Infectious Disease [J].
Attanasio, John ;
Wherry, E. John .
IMMUNITY, 2016, 44 (05) :1052-1068
[4]   Restoring function in exhausted CD8 T cells during chronic viral infection [J].
Barber, DL ;
Wherry, EJ ;
Masopust, D ;
Zhu, BG ;
Allison, JP ;
Sharpe, AH ;
Freeman, GJ ;
Ahmed, R .
NATURE, 2006, 439 (7077) :682-687
[5]   Chimeric Antigen Receptor- and TCR-Modified T Cells Enter Main Street and Wall Street [J].
Barrett, David M. ;
Grupp, Stephan A. ;
June, Carl H. .
JOURNAL OF IMMUNOLOGY, 2015, 195 (03) :755-761
[6]   Bioenergetic Insufficiencies Due to Metabolic Alterations Regulated by the Inhibitory Receptor PD-1 Are an Early Driver of CD8+ T Cell Exhaustion [J].
Bengsch, Bertram ;
Johnson, Andy L. ;
Kurachi, Makoto ;
Odorizzi, Pamela M. ;
Pauken, Kristen E. ;
Attanasio, John ;
Stelekati, Erietta ;
McLane, Laura M. ;
Paley, Michael A. ;
Delgoffe, Greg M. ;
Wherry, E. John .
IMMUNITY, 2016, 45 (02) :358-373
[7]   Restoration of HBV-specific CD8+T cell function by PD-1 blockade in inactive carrier patients is linked to T cell differentiation [J].
Bengsch, Bertram ;
Martin, Bianca ;
Thimme, Robert .
JOURNAL OF HEPATOLOGY, 2014, 61 (06) :1212-1219
[8]   T-cell therapy for chronic viral hepatitis [J].
Bertoletti, Antonio ;
Tan, Anthony Tanoto ;
Koh, Sarene .
CYTOTHERAPY, 2017, 19 (11) :1317-1324
[9]   Adaptive immunity in HBV infection [J].
Bertoletti, Antonio ;
Ferrari, Carlo .
JOURNAL OF HEPATOLOGY, 2016, 64 :S71-S83
[10]   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