Hepatitis C virus vaccine candidates inducing protective neutralizing antibodies

被引:53
作者
Fauvelle, Catherine [1 ,2 ]
Colpitts, Che C. [1 ,2 ]
Keck, Zhen-yong [3 ]
Pierce, Brian G. [4 ]
Foung, Steven K. H. [3 ]
Baumert, Thomas F. [1 ,2 ,5 ]
机构
[1] Inst Rech Malad Virales & Hepat, INSERM, U1110, Strasbourg, France
[2] Univ Strasbourg, Strasbourg, France
[3] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA USA
[4] Univ Maryland, Inst Biosci & Biotechnol Res, Rockville, MD USA
[5] Hopitaux Univ Strasbourg, Pole Hepato Digestif, Inst Hosp Univ, Strasbourg, France
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
Hepatitis C; vaccine; immunity; antibodies; E2 ENVELOPE GLYCOPROTEIN; SUSTAINED VIROLOGICAL RESPONSE; HUMAN MONOCLONAL-ANTIBODIES; CELLULAR IMMUNE-RESPONSES; HCV INFECTION; CD81; BINDING; LIVER-TRANSPLANTATION; THERAPEUTIC VACCINES; HYPERVARIABLE REGION; VIRAL CLEARANCE;
D O I
10.1080/14760584.2016.1194759
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: With more than 150 million chronically infected people, hepatitis C virus (HCV) remains a substantial global health burden. Direct-acting antivirals have dramatically improved viral cure. However, limited access to therapy, late stage detection of infection and re-infection following cure illustrate the need for a vaccine for global control of infection. Vaccines with induction of neutralizing antibodies (nAbs) have been shown to protect successfully against infections by multiple viruses and are currently developed for HCV. Areas covered: Here we review the progress towards the development of vaccines aiming to confer protection against chronic HCV infection by inducing broadly nAbs. The understanding or viral immune evasion in infected patients, the development of novel model systems and the recent structural characterization of viral envelope glycoprotein E2 has markedly advanced our understanding of the molecular mechanisms of virus neutralization with the concomitant development of several vaccine candidates. Expert commentary: While HCV vaccine development remains challenged by the high viral diversity and immune evasion, marked progress in HCV research has advanced vaccine design. Several vaccine candidates have shown robust induction of nAbs in animal models and humans. Randomized clinical trials are the next step to assess their clinical efficacy for protection against chronic infection.
引用
收藏
页码:1535 / 1544
页数:10
相关论文
共 115 条
[1]   Neutralizing Antibodies Induced by Cell Culture-Derived Hepatitis C Virus Protect Against Infection in Mice [J].
Akazawa, Daisuke ;
Moriyama, Masaki ;
Yokokawa, Hiroshi ;
Omi, Noriaki ;
Watanabe, Noriyuki ;
Date, Tomoko ;
Morikawa, Kenichi ;
Aizaki, Hideki ;
Ishii, Koji ;
Kato, Takanobu ;
Mochizuki, Hidenori ;
Nakamura, Noriko ;
Wakita, Takaji .
GASTROENTEROLOGY, 2013, 145 (02) :447-+
[2]   Recombinant Hepatitis C Virus Envelope Glycoprotein Vaccine Elicits Antibodies Targeting Multiple Epitopes on the Envelope Glycoproteins Associated with Broad Cross-Neutralization [J].
Alexander, Jason ;
Wong, Ji-Xhin ;
Bhat, Rakesh ;
Hockman, Darren ;
Logan, Michael ;
Chen, Chao ;
Levin, Aviad ;
Frey, Sharon E. ;
Belshe, Robert B. ;
Tyrrell, D. Lorne ;
Law, John Lok Man ;
Houghton, Michael .
JOURNAL OF VIROLOGY, 2014, 88 (24) :14278-14288
[3]   Monoclonal Antibodies Directed toward the Hepatitis C Virus Glycoprotein E2 Detect Antigenic Differences Modulated by the N-Terminal Hypervariable Region 1 (HVR1), HVR2, and Intergenotypic Variable Region [J].
Alhammad, Yousef ;
Gu, Jun ;
Boo, Irene ;
Harrison, David ;
McCaffrey, Kathleen ;
Vietheer, Patricia T. ;
Edwards, Stirling ;
Quinn, Charles ;
Coulibaly, Fasseli ;
Poumbourios, Pantelis ;
Drummer, Heidi E. .
JOURNAL OF VIROLOGY, 2015, 89 (24) :12245-12261
[4]   Immunogenicity of CIGB-230, a therapeutic DNA vaccine preparation, in HCV-chronically infected individuals in a Phase I clinical trial [J].
Alvarez-Lajonchere, L. ;
Shoukry, N. H. ;
Gra, B. ;
Amador-Canizares, Y. ;
Helle, F. ;
Bedard, N. ;
Guerra, I. ;
Drouin, C. ;
Dubuisson, J. ;
Gonzalez-Horta, E. E. ;
Martinez, G. ;
Marante, J. ;
Cinza, Z. ;
Castellanos, M. ;
Duenas-Carrera, S. .
JOURNAL OF VIRAL HEPATITIS, 2009, 16 (03) :156-167
[5]   Characterization of low- and very-low-density hepatitis C virus RNA-containing particles [J].
André, P ;
Komurian-Pradel, F ;
Deforges, S ;
Perret, M ;
Berland, JL ;
Sodoyer, M ;
Pol, S ;
Bréchot, C ;
Paranhos-Baccalà, G ;
Lotteau, V .
JOURNAL OF VIROLOGY, 2002, 76 (14) :6919-6928
[6]   The past, present and future of neutralizing antibodies for hepatitis C virus [J].
Ball, Jonathan K. ;
Tarr, Alexander W. ;
McKeating, Jane A. .
ANTIVIRAL RESEARCH, 2014, 105 :100-111
[7]   Hepatitis C Virus Hypervariable Region 1 Modulates Receptor Interactions, Conceals the CD81 Binding Site, and Protects Conserved Neutralizing Epitopes [J].
Bankwitz, Dorothea ;
Steinmann, Eike ;
Bitzegeio, Julia ;
Ciesek, Sandra ;
Friesland, Martina ;
Herrmann, Eva ;
Zeisel, Mirjam B. ;
Baumert, Thomas F. ;
Keck, Zhen-yong ;
Foung, Steven K. H. ;
Pecheur, Eve-Isabelle ;
Pietschmann, Thomas .
JOURNAL OF VIROLOGY, 2010, 84 (11) :5751-5763
[8]   Infectious hepatitis C virus pseudo-particles containing functional E1-E2 envelope protein complexes [J].
Bartosch, B ;
Dubuisson, J ;
Cosset, FL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (05) :633-642
[9]   Hepatitis C virus structural proteins assemble into viruslike particles in insect cells [J].
Baumert, TF ;
Ito, S ;
Wong, DT ;
Liang, TJ .
JOURNAL OF VIROLOGY, 1998, 72 (05) :3827-3836
[10]   A prophylactic hepatitis C virus vaccine: A distant peak still worth climbing [J].
Baumert, Thomas F. ;
Fauvelle, Catherine ;
Chen, Diana Y. ;
Lauer, Georg M. .
JOURNAL OF HEPATOLOGY, 2014, 61 :S34-S44