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Immunological responses following administration of a genotype 1a/1b/2/3a quadrivalent HCV VLP vaccine.
Christiansen, D; Earnest-Silveira, L; Chua, B; Meuleman, P; Boo, I; Grubor-Bauk, B; Jackson, D C; Keck, Z Y; Foung, S K H; Drummer, H E; Gowans, E J; Torresi, J.
Affiliation
  • Christiansen D; Department of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Earnest-Silveira L; Department of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Chua B; Department of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Meuleman P; Laboratory of Liver Infectious Diseases, Faculty of Medicine and Health Sciences, Ghent University, De Pintelaan 185, 9000, Ghent, Belgium.
  • Boo I; Burnet Institute, Melbourne, Australia.
  • Grubor-Bauk B; Department of Surgery, The University of Adelaide and The Basil Hetzel Institute for Translational Health Research, Adelaide, South Australia, Australia.
  • Jackson DC; Department of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Keck ZY; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Foung SKH; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Drummer HE; Department of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Gowans EJ; Burnet Institute, Melbourne, Australia.
  • Torresi J; Department of Microbiology, Monash University, Clayton, Australia.
Sci Rep ; 8(1): 6483, 2018 04 24.
Article in En | MEDLINE | ID: mdl-29691437
ABSTRACT
The significant public health problem of Hepatitis C virus (HCV) has been partially addressed with the advent of directly acting antiviral agents (DAAs). However, the development of an effective preventative vaccine would have a significant impact on HCV incidence and would represent a major advance towards controlling and possibly eradicating HCV globally. We previously reported a genotype 1a HCV viral-like particle (VLP) vaccine that produced neutralizing antibodies (NAb) and T cell responses to HCV. To advance this approach, we produced a quadrivalent genotype 1a/1b/2a/3a HCV VLP vaccine to produce broader immune responses. We show that this quadrivalent vaccine produces antibody and NAb responses together with strong T and B cell responses in vaccinated mice. Moreover, selective neutralizing human monoclonal antibodies (HuMAbs) targeting conserved antigenic domain B and D epitopes of the E2 protein bound strongly to the HCV VLPs, suggesting that these critical epitopes are expressed on the surface of the particles. Our findings demonstrate that a quadrivalent HCV VLP based vaccine induces broad humoral and cellular immune responses that will be necessary for protection against HCV. Such a vaccine could provide a substantial addition to highly active antiviral drugs in eliminating HCV.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viral Hepatitis Vaccines / Hepatitis C / Hepacivirus Limits: Animals Language: En Journal: Sci Rep Year: 2018 Document type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viral Hepatitis Vaccines / Hepatitis C / Hepacivirus Limits: Animals Language: En Journal: Sci Rep Year: 2018 Document type: Article Affiliation country: Australia