Copyright
©The Author(s) 2017.
World J Hepatol. Nov 28, 2017; 9(33): 1239-1252
Published online Nov 28, 2017. doi: 10.4254/wjh.v9.i33.1239
Published online Nov 28, 2017. doi: 10.4254/wjh.v9.i33.1239
Type of vaccine | Vaccine structure/adjuvant | Stage of development | Outcome | Application | Developer | Year | Current status | Ref. |
Recombinant protein vaccine | Recombinant E1 or E2/MF59 | 7 chimpanzees | Induce strong humoral immune response; complete protection in 5 chimpanzees | Prophylactic vaccine | Chiron/ Novartis | 1994 | Completed | [101] |
Recombinant E1 or E2/Alum | 4 Chimpanzees | Induce antigen-specific T-helper cytokines in either E1 or | Therapeutic vaccine | BPRC | 2011 | Published | [102] | |
Recombinant E1/Alum | Phase I 20 healthy volunteers | E2-vaccinated animals; clear HCV infection in only E1-vaccinated animals (neutralizing antibodies) Induce strong cellular and humoral anti-E1 responses | Therapeutic vaccine | Fujirebio Europe | 2004 | Published | [103] | |
Recombinant E1 and E2/MF59 | Phase I 60 healthy volunteers | Induce humoral and cellular immune responses | Prophylactic vaccine | Novartis | 2010 | Completed | [104] | |
Recombinant E1/Alum | Phase I/II 20 healthy volunteers and 35 patients with chronic HCV infection/122 HCV-infected patients | Induce HCV specific humoral and cellular immune responses (Th1 type); no change in HCV viral load | Therapeutic vaccine | Innogenetics/ GenImmune | 2003/2008 | Published | [103,105,106] | |
HCV core protein/ISCOMATRIX | Phase I/IIa 30 healthy volunteers | Induce strong humoral immune responses in all except one patients; induce CD8+ T cell responses in 2 of 8 patients receiving the highest dose | Prophylactic vaccine | CSL Ltd | 2009 | Published | [107] | |
GI5005: Inactivated recombinant Saccharomyces cerevisiae expressing NS3-core fusion protein/ GI-5005 plus SOC | Phase I/II 66 patients with chronic HCV infection/ | Improve SVR | Therapeutic vaccine | GlobeImmune | 2009/2010 | Completed | [108,109] | |
Peptide-based vaccine | Peptide from core protein (C35-C44)/ISA51 | Phase I 26 patients with chronic HCV infection | Induce peptide-specific cellular and humoral immune responses in 15 of 25 patients; decline HCV viral load in 2 of 25 patients | Therapeutic vaccine | Karume University | 2009 | Published | [110] |
Four peptides from E1, E2, NS3 and NS5A/Freund’s adjuvant | Phase I 12 nonresponder patients with chronic HCV infection | Induce peptide-specific cellular and humoral immune responses; decline HCV viral load in 3 patients | Therapeutic vaccine | Karume University | 2007 | Published | [111] | |
Autologous dendritic cell delivered six CD8+ T cell epitope peptides from core, NS3 and NS4B | Phase I 6 nonresponder patients with chronic HCV infection | Induce transient T-cell response | Therapeutic vaccine | Burnet Institute + others | 2010 | Completed | [112] | |
IC41: Five peptides from core, NS3, and NS4/Poly-L-arginine | Phase I/II 128 volunteers/60 non-responders with chronic HCV infection | Induce HCV-specific T-cell responses | Therapeutic vaccine | Intercell AG | 2006/2008 | Published | [113,114] | |
IC41/Poly-L-arginine + imiquimod | Phase I 54 healthy volunteers | Induce significant T cell responses; low immunogenicity of topical imiquimod | Therapeutic vaccine | Intercell AG | 2010 | Published | [115] | |
IC41 + imiquimod | Phase II 50 HCV-infected patients | Decline viral load; induce T cell responses | Therapeutic vaccine | Intercell AG | 2012 | Completed | [116] | |
Virus-like particles | Recombinant HCV-like particles (HCV-LPs) containing core, E1, and E2/AS01B | 4 chimpanzees | Induce HCV-specific cellular immune responses; viral clearance | Prophylactic vaccine | NIH | 2007 | Published | [117] |
Recombinant baculovirus containing core, E1 and E2 | Mice | Induce high titers of anti-E2 antibodies and strong HCV-specific cellular immune responses (CD8+ T and Th1 cells) | Prophylactic vaccine | NIH | 2001 | Published | [118] | |
Bacterial-vectored vaccine | Attenuated Salmonella typhimurium containing NS3 gene | Mice | Induce long-lasting T-cell responses | Therapeutic vaccine | NIH | 2001 | Published | [119] |
Viral-vectored vaccine | Recombinant adenoviral vectors and plasmid DNA expressing NS3-NS5B | 5 chimpanzees | Induce memory HCV-specific T cells; control of viremia | Prophylactic vaccine | NIH/Okairos | 2012 | Completed | [120] |
Multiple adenoviral vectors (Ad5, Ad6, Ad24, ChAd32 and ChAd33) expressing NS3-NS5B proteins | Mice and rhesus macaque | Induce strong cellular immune responses; long-term maintenance of memory cells | Prophylactic vaccine | Okairos | 2006 | Published | [121] | |
Recombinant vaccinia viruses (rVV) expressing core, E1, E2, P7, NS2 and NS3 | 4 chimpanzees | Induce cellular immune responses; reduce viral load; resolve HCV infection | Prophylactic vaccine | NYC Blood Center | 2008 | Published | [122] | |
Recombinant adenoviral vectors (Ad6 and ChAd3) expressing NS3-NS5B proteins | Phase I 40 healthy volunteers | Induce sustained HCV-specific T cell responses | Prophylactic vaccine | Okairos | 2012 | Completed | [123] | |
Adenovirus vector (Ad6 and ChAd3) expressing NS3-NS5B proteins | Phase I 36 healthy volunteers | Highly immunogenic; induce HCV specific T cell responses | Prophylactic vaccine | Okairos and Oxford University | 2009 | Published | [124] | |
TG4040: MVA vector expressing NS3, NS4 and NS5B proteins | Phase I 15 patients with chronic HCV infection | Decline HCV viral load in 7 of 15 patients associated with T-cell response | Therapeutic vaccine | Transgene | 2009 | Withdrawn | [125] | |
MVA and ChAd3 vectors expressing NS3, NS4, NS5A and NS5B proteins | Phase I/II Healthy at risk population (68/472 IDU) | July 28, 2018: Final data collection date | Prophylactic vaccine | NIAID | 2017 | Ongoing | [126] | |
TG4040 + SOC | Phase II 153 patients with chronic HCV infection | Induce HCV- and MVA-specific T-cell responses; develop anti-MVA antibodies; increase rate of early virologic response | Therapeutic vaccine | - | 2014 | Published | [127] | |
DNA vaccine | Recombinant DNA plasmid encoding E2 | 2 chimpanzees | Induce humoral and cellular immune responses; resolve the infection; prevent progression to chronicity | Prophylactic vaccine | NIAID/NIH | 2000 | Published | [128] |
Recombinant DNA plasmid and adenovirus vector expressing core, E1, E2 and NS3-5 | 8 chimpanzees | Induce HCV-specific T-cell and long-lasting E2-specific antibody responses; reduce viral load | Prophylactic vaccine | NIH | 2005 | Published | [129] | |
Recombinant DNA plasmids and MVA vector expressing core, E1, E2 and NS3 | 6 chimpanzees | Induce HCV-specific immune responses; reduce viral load; early control of acute HCV infection; fail to impact on chronicity | Prophylactic vaccine | Transgene | 2007 | Published | [130] | |
CIGB-230: Plasmid expressing core/E1/E2 plus recombinant core protein | Phase I 15 non-responder patients with chronic HCV infection | Induce humoral and cellular immune responses; no viral clearance | Therapeutic vaccine | University of Montreal + others | 2009 | Published | [131] | |
ChronVac-C: Plasmid expressing NS3 and NS4A delivered by in vivo electroporation | Phase I/IIa 12 HCV-infected patients | Decline HCV viral load in 4 of 6 patients receiving the highest dose with corresponding HCV-specific T-cell response in 3 patients | Therapeutic vaccine | Tripep AB | 2009 | Recruiting | [132] |
- Citation: Taherkhani R, Farshadpour F. Global elimination of hepatitis C virus infection: Progresses and the remaining challenges. World J Hepatol 2017; 9(33): 1239-1252
- URL: https://www.wjgnet.com/1948-5182/full/v9/i33/1239.htm
- DOI: https://dx.doi.org/10.4254/wjh.v9.i33.1239