Yellow Fever Virus: Knowledge Gaps Impeding the Fight Against an Old Foe

被引:113
作者
Douam, Florian [1 ]
Ploss, Alexander [1 ]
机构
[1] Princeton Univ, Dept Mol Biol, Lewis Thomas Lab, 110 Lewis Thomas Lab,Washington Rd, Princeton, NJ 08544 USA
基金
美国国家卫生研究院;
关键词
17D VACCINE VIRUS; DENGUE VIRUS; MACACUS-RHESUS; NS2B-NS3; PROTEASE; COMPLEX-FORMATION; IMMUNE-RESPONSE; CELL RESPONSE; CLEAVAGE SITE; IN-VITRO; T-CELLS;
D O I
10.1016/j.tim.2018.05.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Yellow fever (YF) was one of the most dangerous infectious diseases of the 18th and 19th centuries, resulting in mass casualties in Africa and the Americas. The etiologic agent is yellow fever virus (YFV), and its live-attenuated form, YFV-17D, remains one of the most potent vaccines ever developed. During the first half of the 20th century, vaccination combined with mosquito control eradicated YFV transmission in urban areas. However, the recent 2016-2018 outbreaks in areas with historically low or no YFV activity have raised serious concerns for an estimated 400-500 million unvaccinated people who now live in at-risk areas. Once a forgotten disease, we highlight here that YF still represents a very real threat to human health and economies. As many gaps remain in our understanding of how YFV interacts with the human host and causes disease, there is an urgent need to address these knowledge gaps and propel YFV research forward.
引用
收藏
页码:913 / 928
页数:16
相关论文
共 112 条
[1]   Yellow fever from Angola and Congo: a storm gathers [J].
Ahmed, Qanta A. ;
Memish, Ziad A. .
TROPICAL DOCTOR, 2017, 47 (02) :92-96
[2]  
Ahuka-Mundeke S., 2018, N Engl J Med, DOI DOI 10.1056/NEJMOA1710430
[3]   Origin and differentiation of human memory CD8 T cells after vaccination [J].
Akondy, Rama S. ;
Fitch, Mark ;
Edupuganti, Srilatha ;
Yang, Shu ;
Kissick, Haydn T. ;
Li, Kelvin W. ;
Youngblood, Ben A. ;
Abdelsamed, Hossam A. ;
McGuire, Donald J. ;
Cohen, Kristen W. ;
Alexe, Gabriela ;
Nagar, Shashi ;
McCausland, Megan M. ;
Gupta, Satish ;
Tata, Pramila ;
Haining, W. Nicholas ;
McElrath, M. Juliana ;
Zhang, David ;
Hu, Bin ;
Greenleaf, William J. ;
Goronzy, Jorg J. ;
Mulligan, Mark J. ;
Hellerstein, Marc ;
Ahmed, Rafi .
NATURE, 2017, 552 (7685) :362-+
[4]   Initial viral load determines the magnitude of the human CD8 T cell response to yellow fever vaccination [J].
Akondy, Rama S. ;
Johnson, Philip L. F. ;
Nakaya, Helder I. ;
Edupuganti, Srilatha ;
Mulligan, Mark J. ;
Lawson, Benton ;
Miller, Joseph D. ;
Pulendran, Bali ;
Antia, Rustom ;
Ahmed, Rafi .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (10) :3050-3055
[5]   The Yellow Fever Virus Vaccine Induces a Broad and Polyfunctional Human Memory CD8+ T Cell Response [J].
Akondy, Rama S. ;
Monson, Nathan D. ;
Miller, Joseph D. ;
Edupuganti, Srilatha ;
Teuwen, Dirk ;
Wu, Hong ;
Quyyumi, Farah ;
Garg, Seema ;
Altman, John D. ;
Del Rio, Carlos ;
Keyserling, Harry L. ;
Ploss, Alexander ;
Rice, Charles M. ;
Orenstein, Walter A. ;
Mulligan, Mark J. ;
Ahmed, Rafi .
JOURNAL OF IMMUNOLOGY, 2009, 183 (12) :7919-7930
[6]   Mutagenesis of the NS2B-NS3-mediated cleavage site in the flavivirus capsid protein demonstrates a requirement for coordinated processing [J].
Amberg, SM ;
Rice, CM .
JOURNAL OF VIROLOGY, 1999, 73 (10) :8083-8094
[7]  
[Anonymous], 2017, Wkly Epidemiol Rec, V92, P193
[8]  
[Anonymous], 2017, Wkly Epidemiol Rec, V92, P442
[9]   Coupling of replication and assembly in flaviviruses [J].
Apte-Sengupta, Swapna ;
Sirohi, Devika ;
Kuhn, Richard J. .
CURRENT OPINION IN VIROLOGY, 2014, 9 :134-142
[10]   Live attenuated yellow fever 17D infects human DCs and allows for presentation of endogenous and recombinant T cell epitopes [J].
Barba-Spaeth, G ;
Longman, RS ;
Albert, ML ;
Rice, CM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (09) :1179-1184