» Articles » PMID: 15194776

Immunization with Hepatitis C Virus-like Particles Induces Humoral and Cellular Immune Responses in Nonhuman Primates

Overview
Journal J Virol
Date 2004 Jun 15
PMID 15194776
Citations 42
Authors
Affiliations
Soon will be listed here.
Abstract

We have previously reported the production of hepatitis C virus-like particles (HCV-LP) using a recombinant baculovirus containing the cDNA of the HCV structural proteins (core, E1, and E2). These particles resemble the putative HCV virions and are capable of inducing strong and broad humoral and cellular immune responses in mice. Here we present evidence on the immunogenicity of HCV-LP and the effects of novel adjuvant systems in a nonhuman primate model, the baboon. Three groups of four baboons were immunized with HCV-LP, HCV-LP and adjuvant AS01B (monophosphoryl lipid A and QS21), or HCV-LP and the combination of AS01B and CpG oligodeoxynucleotides 10105. After four immunizations over an 8-month period, all animals developed HCV-specific humoral and cellular immune responses including antibodies to HCV structural proteins and gamma interferon(+) (IFN-gamma(+))CD4(+) and IFN-gamma(+)CD8(+) T-cell responses. The immunogenicity of HCV-LP was only marginally enhanced by the use of adjuvants. The overall HCV-specific immune responses were broad and long lasting. Our results suggest that HCV-LP is a potent immunogen to induce HCV-specific humoral and cellular immune responses in primates and may be a promising approach to develop novel preventive and therapeutic modalities.

Citing Articles

Recent Advances in Antiviral Drug Delivery Strategies.

Rana D, Prajapati A, Karunakaran B, Vora L, Benival D, Jindal A AAPS PharmSciTech. 2025; 26(3):73.

PMID: 40038154 DOI: 10.1208/s12249-025-03053-3.


Virus-Mimicking Polymer Nanocomplexes Co-Assembling HCV E1E2 and Core Proteins with TLR 7/8 Agonist-Synthesis, Characterization, and In Vivo Activity.

Fuerst T, Marin A, Jeong S, Kulakova L, Hlushko R, Gorga K J Funct Biomater. 2025; 16(1).

PMID: 39852590 PMC: 11766188. DOI: 10.3390/jfb16010034.


[Development approaches for vaccines against hepatitis C virus infections].

Bankwitz D, Krey T, Pietschmann T Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2022; 65(2):183-191.

PMID: 35015104 PMC: 8749110. DOI: 10.1007/s00103-021-03477-9.


Viral hepatitis update: Progress and perspectives.

Pisano M, Giadans C, Flichman D, Re V, Preciado M, Valva P World J Gastroenterol. 2021; 27(26):4018-4044.

PMID: 34326611 PMC: 8311538. DOI: 10.3748/wjg.v27.i26.4018.


Immunopotentiating and Delivery Systems for HCV Vaccines.

Andrianov A, Fuerst T Viruses. 2021; 13(6).

PMID: 34070543 PMC: 8227888. DOI: 10.3390/v13060981.


References
1.
Paliard X, Liu Y, Wagner R, Wolf H, Baenziger J, Walker C . Priming of strong, broad, and long-lived HIV type 1 p55gag-specific CD8+ cytotoxic T cells after administration of a virus-like particle vaccine in rhesus macaques. AIDS Res Hum Retroviruses. 2000; 16(3):273-82. DOI: 10.1089/088922200309368. View

2.
Weeratna R, McCluskie M, Xu Y, Davis H . CpG DNA induces stronger immune responses with less toxicity than other adjuvants. Vaccine. 2000; 18(17):1755-62. DOI: 10.1016/s0264-410x(99)00526-5. View

3.
Lechner F, Wong D, Dunbar P, Chapman R, Chung R, Dohrenwend P . Analysis of successful immune responses in persons infected with hepatitis C virus. J Exp Med. 2000; 191(9):1499-512. PMC: 2213430. DOI: 10.1084/jem.191.9.1499. View

4.
Takaki A, Wiese M, Maertens G, Depla E, Seifert U, Liebetrau A . Cellular immune responses persist and humoral responses decrease two decades after recovery from a single-source outbreak of hepatitis C. Nat Med. 2000; 6(5):578-82. DOI: 10.1038/75063. View

5.
Forns X, Payette P, Ma X, Satterfield W, Eder G, MUSHAHWAR I . Vaccination of chimpanzees with plasmid DNA encoding the hepatitis C virus (HCV) envelope E2 protein modified the infection after challenge with homologous monoclonal HCV. Hepatology. 2000; 32(3):618-25. DOI: 10.1053/jhep.2000.9877. View