Immunogenicity and safety of a novel therapeutic hepatitis C virus (HCV) peptide vaccine: A randomized, placebo controlled trial for dose optimization in 128 healthy subjects

As interferon/ribavirin-based standard therapy is curative in only about half of HCV patients, there remains an important need for alternatives including vaccines. The novel peptide vaccine IC41 consists of five synthetic peptides harboring HCV T cell epitopes and poly- l-arginine as synthetic adjuv...

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Published inVaccine Vol. 24; no. 20; pp. 4343 - 4353
Main Authors Firbas, Christa, Jilma, Bernd, Tauber, Erich, Buerger, Vera, Jelovcan, Sandra, Lingnau, Karen, Buschle, Michael, Frisch, Jürgen, Klade, Christoph S.
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 15.05.2006
Elsevier
Elsevier Limited
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Online AccessGet full text
ISSN0264-410X
1873-2518
DOI10.1016/j.vaccine.2006.03.009

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Abstract As interferon/ribavirin-based standard therapy is curative in only about half of HCV patients, there remains an important need for alternatives including vaccines. The novel peptide vaccine IC41 consists of five synthetic peptides harboring HCV T cell epitopes and poly- l-arginine as synthetic adjuvant. In this randomized, placebo-controlled trial, 128 HLA-A2 positive healthy volunteers received four s.c. vaccinations of seven different doses IC41, HCV peptides alone, poly- l-arginine alone or saline solution, every 4 weeks. IC41 was safe and well tolerated. Mild to moderate local reactions were transient. Immunogenicity was assessed using T cell epitope specific [ 3H]-thymidine proliferation, IFN-gamma ELIspot and HLA-tetramer assays. IC41 induced responses in all dose groups. Higher responder rates were recorded in higher dose groups and increasing number of vaccinations were associated with higher responder rates and more robust responses. Poly- l-arginine was required for the aimed-for Th1/Tc1-type immunity (IFN-gamma secreting T cells).
AbstractList As interferon/ribavirin-based standard therapy is curative in only about half of HCV patients, there remains an important need for alternatives including vaccines. The novel peptide vaccine IC41 consists of five synthetic peptides harboring HCV T cell epitopes and poly-l-arginine as synthetic adjuvant. In this randomized, placebo-controlled trial, 128 HLA-A2 positive healthy volunteers received four s.c. vaccinations of seven different doses IC41, HCV peptides alone, poly-l-arginine alone or saline solution, every 4 weeks. IC41 was safe and well tolerated. Mild to moderate local reactions were transient. Immunogenicity was assessed using T cell epitope specific [3H]-thymidine proliferation, IFN-gamma ELIspot and HLA-tetramer assays. IC41 induced responses in all dose groups. Higher responder rates were recorded in higher dose groups and increasing number of vaccinations were associated with higher responder rates and more robust responses. Poly-l-arginine was required for the aimed-for Th1/Tc1-type immunity (IFN-gamma secreting T cells).
As interferon/ribavirin-based standard therapy is curative in only about half of HCV patients, there remains an important need for alternatives including vaccines. The novel peptide vaccine IC41 consists of five synthetic peptides harboring HCV T cell epitopes and poly- l-arginine as synthetic adjuvant. In this randomized, placebo-controlled trial, 128 HLA-A2 positive healthy volunteers received four s.c. vaccinations of seven different doses IC41, HCV peptides alone, poly- l-arginine alone or saline solution, every 4 weeks. IC41 was safe and well tolerated. Mild to moderate local reactions were transient. Immunogenicity was assessed using T cell epitope specific [ 3H]-thymidine proliferation, IFN-gamma ELIspot and HLA-tetramer assays. IC41 induced responses in all dose groups. Higher responder rates were recorded in higher dose groups and increasing number of vaccinations were associated with higher responder rates and more robust responses. Poly- l-arginine was required for the aimed-for Th1/Tc1-type immunity (IFN-gamma secreting T cells).
As interferon/ribavirin-based standard therapy is curative in only about half of HCV patients, there remains an important need for alternatives including vaccines. The novel peptide vaccine IC41 consists of five synthetic peptides harboring HCV T cell epitopes and poly-L-arginine as synthetic adjuvant. In this randomized, placebo-controlled trial, 128 HLA-A2 positive healthy volunteers received four s.c. vaccinations of seven different doses IC41, HCV peptides alone, poly-l-arginine alone or saline solution, every 4 weeks. IC41 was safe and well tolerated. Mild to moderate local reactions were transient. Immunogenicity was assessed using T cell epitope specific [3H]-thymidine proliferation, IFN-gamma ELIspot and HLA-tetramer assays. IC41 induced responses in all dose groups. Higher responder rates were recorded in higher dose groups and increasing number of vaccinations were associated with higher responder rates and more robust responses. Poly-L-arginine was required for the aimed-for Th1/Tc1-type immunity (IFN-gamma secreting T cells).As interferon/ribavirin-based standard therapy is curative in only about half of HCV patients, there remains an important need for alternatives including vaccines. The novel peptide vaccine IC41 consists of five synthetic peptides harboring HCV T cell epitopes and poly-L-arginine as synthetic adjuvant. In this randomized, placebo-controlled trial, 128 HLA-A2 positive healthy volunteers received four s.c. vaccinations of seven different doses IC41, HCV peptides alone, poly-l-arginine alone or saline solution, every 4 weeks. IC41 was safe and well tolerated. Mild to moderate local reactions were transient. Immunogenicity was assessed using T cell epitope specific [3H]-thymidine proliferation, IFN-gamma ELIspot and HLA-tetramer assays. IC41 induced responses in all dose groups. Higher responder rates were recorded in higher dose groups and increasing number of vaccinations were associated with higher responder rates and more robust responses. Poly-L-arginine was required for the aimed-for Th1/Tc1-type immunity (IFN-gamma secreting T cells).
As interferon/ribavirin-based standard therapy is curative in only about half of HCV patients, there remains an important need for alternatives including vaccines. The novel peptide vaccine IC41 consists of five synthetic peptides harboring HCV T cell epitopes and poly-l-arginine as synthetic adjuvant. In this randomized, placebo-controlled trial, 128 HLA-A2 positive healthy volunteers received four s.c. vaccinations of seven different doses IC41, HCV peptides alone, poly-l-arginine alone or saline solution, every 4 weeks. IC41 was safe and well tolerated. Mild to moderate local reactions were transient. Immunogenicity was assessed using T cell epitope specific [ super(3)H]-thymidine proliferation, IFN-gamma ELIspot and HLA-tetramer assays. IC41 induced responses in all dose groups. Higher responder rates were recorded in higher dose groups and increasing number of vaccinations were associated with higher responder rates and more robust responses. Poly-l-arginine was required for the aimed-for Th1/Tc1-type immunity (IFN-gamma secreting T cells).
Author Tauber, Erich
Lingnau, Karen
Jilma, Bernd
Firbas, Christa
Buerger, Vera
Buschle, Michael
Jelovcan, Sandra
Frisch, Jürgen
Klade, Christoph S.
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  givenname: Bernd
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  fullname: Jilma, Bernd
  email: bernd.jilma@meduniwien.ac.at
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  givenname: Erich
  surname: Tauber
  fullname: Tauber, Erich
  organization: Intercell AG, Vienna Biocenter Campus, A-1030 Vienna, Austria
– sequence: 4
  givenname: Vera
  surname: Buerger
  fullname: Buerger, Vera
  organization: Intercell AG, Vienna Biocenter Campus, A-1030 Vienna, Austria
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  surname: Jelovcan
  fullname: Jelovcan, Sandra
  organization: Intercell AG, Vienna Biocenter Campus, A-1030 Vienna, Austria
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  surname: Lingnau
  fullname: Lingnau, Karen
  organization: Intercell AG, Vienna Biocenter Campus, A-1030 Vienna, Austria
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  surname: Buschle
  fullname: Buschle, Michael
  organization: Intercell AG, Vienna Biocenter Campus, A-1030 Vienna, Austria
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  surname: Frisch
  fullname: Frisch, Jürgen
  organization: Intercell AG, Vienna Biocenter Campus, A-1030 Vienna, Austria
– sequence: 9
  givenname: Christoph S.
  surname: Klade
  fullname: Klade, Christoph S.
  organization: Intercell AG, Vienna Biocenter Campus, A-1030 Vienna, Austria
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ISSN 0264-410X
IngestDate Fri Sep 05 07:18:58 EDT 2025
Fri Sep 05 13:08:26 EDT 2025
Wed Aug 13 04:42:34 EDT 2025
Wed Feb 19 01:48:24 EST 2025
Mon Jul 21 09:14:45 EDT 2025
Tue Jul 01 03:44:52 EDT 2025
Thu Apr 24 23:09:31 EDT 2025
Fri Feb 23 02:32:29 EST 2024
Tue Aug 26 16:34:22 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 20
Keywords Human
Peptide vaccine
Hepatitis C
Randomized controlled trial
Hepatitis A virus
Peptides
Picornaviridae
Toxicity
Hepatic disease
Vaccine
Optimization
Hepatovirus
Infection
Virus
Immunogenicity
Viral disease
Digestive diseases
Flaviviridae
Hepatitis C virus
Hepacivirus
Viral hepatitis C
Language English
License https://www.elsevier.com/tdm/userlicense/1.0
CC BY 4.0
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PQID 1559001626
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Snippet As interferon/ribavirin-based standard therapy is curative in only about half of HCV patients, there remains an important need for alternatives including...
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SubjectTerms Adolescent
Adult
Applied microbiology
Biological and medical sciences
Cell growth
Chronic illnesses
Fundamental and applied biological sciences. Psychology
Hepatitis
Hepatitis C
Hepatitis C - prevention & control
Hepatitis C virus
Human
Human viral diseases
Humans
Immunogenicity
Infections
Infectious diseases
Interferon-gamma - biosynthesis
Lymphocytes
Medical sciences
Microbiology
Middle Aged
Miscellaneous
Mortality
Optimization
Peptide vaccine
Peptides
Placebos
Proteins
Randomized controlled trial
Reference Values
Single-Blind Method
T-Lymphocytes - metabolism
T-Lymphocytes - pathology
Vaccines
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)
Viral diseases
Viral hepatitis
Viral Vaccines - adverse effects
Viral Vaccines - immunology
Virology
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Title Immunogenicity and safety of a novel therapeutic hepatitis C virus (HCV) peptide vaccine: A randomized, placebo controlled trial for dose optimization in 128 healthy subjects
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https://dx.doi.org/10.1016/j.vaccine.2006.03.009
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