Immunotherapy for Chronic Hepatitis B Virus Infection

被引:98
作者
Bertoletti, Antonio [1 ,2 ]
Le Bert, Nina [1 ,2 ]
机构
[1] Duke NUS Med Sch, Emerging Infect Dis Program, 8 Coll Rd, Singapore 169857, Singapore
[2] ASTAR, Viral Hepatitis Lab, Singapore Inst Clin Sci, Singapore, Singapore
关键词
Vaccines; Hepatitis B; chronic; Therapeutics; Hepatitis B virus; CD8(+) T-CELLS; BONE-MARROW-TRANSPLANTATION; ANTIVIRAL IMMUNE-RESPONSE; CHRONIC HBV INFECTION; HEPATOCELLULAR-CARCINOMA; THERAPEUTIC VACCINATION; COMBINATION THERAPY; INTERFERON-ALPHA; SURFACE-ANTIGEN; INNATE IMMUNITY;
D O I
10.5009/gnl17233
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
While new therapies for chronic hepatitis C virus infection have delivered remarkable cure rates, curative therapies for chronic hepatitis B virus (HBV) infection remain a distant goal. Although current direct antiviral therapies are very efficient in controlling viral replication and limiting the progression to cirrhosis, these treatments require lifelong administration due to the frequent viral rebound upon treatment cessation, and immune modulation with interferon is only effective in a subgroup of patients. Specific immunotherapies can offer the possibility of eliminating or at least stably maintaining low levels of HBV replication under the control of a functional host antiviral response. Here, we review the development of immune cell therapy for HBV, highlighting the potential antiviral efficiency and potential toxicities in different groups of chronically infected HBV patients. We also discuss the chronic hepatitis B patient populations that best benefit from therapeutic immune interventions.
引用
收藏
页码:497 / 507
页数:11
相关论文
共 101 条
  • [1] MECHANISMS OF CLASS-I RESTRICTED IMMUNOPATHOLOGY - A TRANSGENIC MOUSE MODEL OF FULMINANT-HEPATITIS
    ANDO, K
    MORIYAMA, T
    GUIDOTTI, LG
    WIRTH, S
    SCHREIBER, RD
    SCHLICHT, HJ
    HUANG, SN
    CHISARI, FV
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (05) : 1541 - 1554
  • [2] IFN-α inhibits HBV transcription and replication in cell culture and in humanized mice by targeting the epigenetic regulation of the nuclear cccDNA minichromosome
    Belloni, Laura
    Allweiss, Lena
    Guerrieri, Francesca
    Pediconi, Natalia
    Volz, Tassilo
    Pollicino, Teresa
    Petersen, Joerg
    Raimondo, Giovanni
    Dandri, Maura
    Levrero, Massimo
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (02) : 529 - 537
  • [3] Restoration of HBV-specific CD8+T cell function by PD-1 blockade in inactive carrier patients is linked to T cell differentiation
    Bengsch, Bertram
    Martin, Bianca
    Thimme, Robert
    [J]. JOURNAL OF HEPATOLOGY, 2014, 61 (06) : 1212 - 1219
  • [4] Adaptive immunity in HBV infection
    Bertoletti, Antonio
    Ferrari, Carlo
    [J]. JOURNAL OF HEPATOLOGY, 2016, 64 : S71 - S83
  • [5] The immune tolerant phase of chronic HBV infection: new perspectives on an old concept
    Bertoletti, Antonio
    Kennedy, Patrick T.
    [J]. CELLULAR & MOLECULAR IMMUNOLOGY, 2015, 12 (03) : 258 - 263
  • [6] Hepatitis B: future curative strategies
    Bertoletti, Antonio
    Rivino, Laura
    [J]. CURRENT OPINION IN INFECTIOUS DISEASES, 2014, 27 (06) : 528 - 534
  • [7] Immune Therapeutic Strategies in Chronic Hepatitis B Virus Infection: Virus or Inflammation Control?
    Bertoletti, Antonio
    Gehring, Adam J.
    [J]. PLOS PATHOGENS, 2013, 9 (12) : 1 - 4
  • [8] Tumor-necrosis factor impairs CD4+ T cell-mediated immunological control in chronic viral infection
    Beyer, Marc
    Abdullah, Zeinab
    Chemnitz, Jens M.
    Maisel, Daniela
    Sander, Jil
    Lehmann, Clara
    Thabet, Yasser
    Shinde, Prashant V.
    Schmidleithner, Lisa
    Koehne, Maren
    Trebicka, Jonel
    Schierwagen, Robert
    Hofmann, Andrea
    Popov, Alexey
    Lang, Karl S.
    Oxenius, Annette
    Buch, Thorsten
    Kurts, Christian
    Heikenwalder, Mathias
    Faetkenheuer, Gerd
    Lang, Philipp A.
    Hartmann, Pia
    Knolle, Percy A.
    Schultze, Joachim L.
    [J]. NATURE IMMUNOLOGY, 2016, 17 (05) : 593 - +
  • [9] Chronic hepatitis B: What should be the goal for new therapies?
    Block, Timothy M.
    Gish, Robert
    Guo, Haitao
    Mehta, Anand
    Cuconati, Andrea
    London, W. Thomas
    Guo, Ju-Tao
    [J]. ANTIVIRAL RESEARCH, 2013, 98 (01) : 27 - 34
  • [10] T cells redirected against hepatitis B virus surface proteins eliminate infected hepatocytes
    Bohne, Felix
    Chmielewski, Markus
    Ebert, Gregor
    Wiegmann, Katja
    Kuerschner, Timo
    Schulze, Andreas
    Urban, Stephan
    Kroenke, Martin
    Abken, Hinrich
    Protzer, Ulrike
    [J]. GASTROENTEROLOGY, 2008, 134 (01) : 239 - 247