Current ebola vaccines

被引:58
作者
Hoenen, Thomas [1 ]
Groseth, Allison [2 ]
Feldmann, Heinz
机构
[1] NIAID, NIH, Div Intramural Res,Lab Virol, Rocky Mt Labs,Dis Modelling & Transmiss Unit, Hamilton, MT USA
[2] NIAID, NIH, Div Intramural Res,Lab Virol, Rocky Mt Labs,Mol Virol & Host Pathogen Interact, Hamilton, MT USA
关键词
ebolavirus; filoviruses; hemorrhagic fever; intervention; vaccine; PROTECTS NONHUMAN-PRIMATES; VIRUS-LIKE PARTICLES; HEMORRHAGIC-FEVER; GUINEA-PIGS; POSTEXPOSURE PROTECTION; MARBURG VIRUS; RESPIRATORY-TRACT; VECTORED VACCINE; DNA VACCINES; MOUSE MODEL;
D O I
10.1517/14712598.2012.685152
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Ebolaviruses cause severe viral hemorrhagic fever in humans and non-human primates (NHPs), with case fatality rates of up to 90%. Currently, neither a specific treatment nor a vaccine licensed for use in humans is available. However, a number of vaccine candidates have been developed in the last decade that are highly protective in NHPs, the gold standard animal model for ebola hemorrhagic fever. Areas covered: This review analyzes a number of scenarios for the use of ebolavirus vaccines, discusses the requirements for ebolavirus vaccines in these scenarios and describes current ebolavirus vaccines. Among these vaccines are recombinant adenoviruses, recombinant vesicular stomatitis viruses (VSVs), recombinant human parainfluenza viruses and virus-like particles. Interestingly, one of these vaccine platforms, based on recombinant VSVs, has also demonstrated post-exposure protection in NHPs. Expert opinion: The most pressing remaining challenge is now to move these vaccine candidates forward into human trials and toward licensure. In order to achieve this, it will be necessary to establish the mechanisms and correlates of protection for these vaccines, and to continue to demonstrate their safety, particularly in potentially immunocompromised populations. However, already now there is sufficient evidence that, from a scientific perspective, a vaccine protective against ebolaviruses is possible.
引用
收藏
页码:859 / 872
页数:14
相关论文
共 91 条
[1]   Defective humoral responses and extensive intravascular apoptosis are associated with fatal outcome in Ebola virus-infected patients [J].
Baize, S ;
Leroy, EM ;
Georges-Courbot, MC ;
Capron, M ;
Lansoud-Soukate, J ;
Debré, P ;
Fisher-Hoch, SP ;
McCormick, JB ;
McCormick, JB ;
Georges, AJ .
NATURE MEDICINE, 1999, 5 (04) :423-426
[2]   Discovery of Swine as a Host for the Reston ebolavirus [J].
Barrette, Roger W. ;
Metwally, Samia A. ;
Rowland, Jessica M. ;
Xu, Lizhe ;
Zaki, Sherif R. ;
Nichol, Stuart T. ;
Rollin, Pierre E. ;
Towner, Jonathan S. ;
Shieh, Wun-Ju ;
Batten, Brigid ;
Sealy, Tara K. ;
Carrillo, Consuelo ;
Moran, Karen E. ;
Bracht, Alexa J. ;
Mayr, Gregory A. ;
Sirios-Cruz, Magdalena ;
Catbagan, Davinio P. ;
Lautner, Elizabeth A. ;
Ksiazek, Thomas G. ;
White, William R. ;
McIntosh, Michael T. .
SCIENCE, 2009, 325 (5937) :204-206
[3]   PATHOLOGY OF EXPERIMENTAL EBOLA VIRUS-INFECTION IN MONKEYS [J].
BASKERVILLE, A ;
BOWEN, ETW ;
PLATT, GS ;
MCARDELL, LB ;
SIMPSON, DIH .
JOURNAL OF PATHOLOGY, 1978, 125 (03) :131-&
[4]   The Organisation of Ebola Virus Reveals a Capacity for Extensive, Modular Polyploidy [J].
Beniac, Daniel R. ;
Melito, Pasquale L. ;
Devarennes, Shauna L. ;
Hiebert, Shannon L. ;
Rabb, Melissa J. ;
Lamboo, Lindsey L. ;
Jones, Steven M. ;
Booth, Timothy F. .
PLOS ONE, 2012, 7 (01)
[5]   Ebola outbreak killed 5000 gorillas [J].
Bermejo, Magdalena ;
Rodriguez-Teijeiro, Jose Domingo ;
Illera, German ;
Barroso, Alex ;
Vila, Carles ;
Walsh, Peter D. .
SCIENCE, 2006, 314 (5805) :1564-1564
[6]   Inactivated or Live-Attenuated Bivalent Vaccines That Confer Protection against Rabies and Ebola Viruses [J].
Blaney, Joseph E. ;
Wirblich, Christoph ;
Papaneri, Amy B. ;
Johnson, Reed F. ;
Myers, Carey J. ;
Juelich, Terry L. ;
Holbrook, Michael R. ;
Freiberg, Alexander N. ;
Bernbaum, John G. ;
Jahrling, Peter B. ;
Paragas, Jason ;
Schnell, Matthias J. .
JOURNAL OF VIROLOGY, 2011, 85 (20) :10605-10616
[7]   EBOLA HEMORRHAGIC-FEVER - EXPERIMENTAL-INFECTION OF MONKEYS [J].
BOWEN, ETW ;
PLATT, GS ;
SIMPSON, DIH ;
MCARDELL, LB ;
RAYMOND, RT .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1978, 72 (02) :188-191
[8]   Haematological, biochemical and coagulation changes in mice, guinea-pigs and monkeys infected with a mouse-adapted variant of Ebola Zaire virus [J].
Bray, M ;
Hatfill, S ;
Hensley, L ;
Huggins, JW .
JOURNAL OF COMPARATIVE PATHOLOGY, 2001, 125 (04) :243-253
[9]   A mouse model for evaluation of prophylaxis and therapy of Ebola hemorrhagic fever [J].
Bray, M ;
Davis, K ;
Geisbert, T ;
Schmaljohn, C ;
Huggins, J .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 :S248-S258
[10]   The role of the Type I interferon response in the resistance of mice to filovirus infection [J].
Bray, M .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :1365-1373