Vaccines against Middle East respiratory syndrome coronavirus for humans and camels

被引:13
作者
Alharbi, Naif Khalaf [1 ,2 ]
机构
[1] KAIMRC, Infect Dis Res Dept, Riyadh, Saudi Arabia
[2] Univ Oxford, Jenner Inst, Oxford, England
关键词
camel vaccine; MERS coronavirus vaccine; Middle East Respiratory Syndrome; RECEPTOR-BINDING DOMAIN; MERS-COV; SPIKE PROTEIN; NEUTRALIZING ANTIBODIES; SAUDI-ARABIA; PROTECTIVE IMMUNITY; DROMEDARY CAMELS; MOUSE MODEL; S-PROTEIN; INFECTION;
D O I
10.1002/rmv.1917
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Middle East respiratory syndrome coronavirus (MERS-CoV) is caused by a novel betacoronavirus that was isolated in late 2012 in Saudi Arabia. The viral infections have been reported in more than 1700 humans, ranging from asymptomatic or mild cases to severe pneumonia with a mortality rate of 40%. It is well documented now that dromedary camels contract the infection and shed the virus without notable symptoms, and such animals had been infected by at least the early 1980s. The mechanism of camel to human transmission is still not clear, but several primary cases have been associated with camel contact. There is no approved antiviral drug or vaccine against MERS-CoV despite the active research in this area. Vaccine candidates have been developed using various platforms and regimens and have been tested in several animal models. Here, this article reviews the published studies on MERS-CoV vaccines with more focus on vaccines tested in large animals, including camels. It is foreseeable that the 1-health approach could be the best way of tackling the MERS-CoV endemic in the Arabian Peninsula, by using the mass vaccination of camels in the affected areas to block camel to human transmission. Camel vaccines can be developed in a faster time with fewer regulations and lower costs and could clear this virus from the Arabian Peninsula if accompanied by efficient public health measures.
引用
收藏
页数:9
相关论文
共 55 条
[1]   Replication and Shedding of MERS-CoV in Upper Respiratory Tract of Inoculated Dromedary Camels [J].
Adney, Danielle R. ;
van Doremalen, Neeltje ;
Brown, Vienna R. ;
Bushmaker, Trenton ;
Scott, Dana ;
de Wit, Emmie ;
Bowen, Richard A. ;
Munster, Vincent J. .
EMERGING INFECTIOUS DISEASES, 2014, 20 (12) :1999-2005
[2]   Generation of a Transgenic Mouse Model of Middle East Respiratory Syndrome Coronavirus Infection and Disease [J].
Agrawal, Anurodh Shankar ;
Garron, Tania ;
Tao, Xinrong ;
Peng, Bi-Hung ;
Wakamiya, Maki ;
Chan, Teh-Sheng ;
Couch, Robert B. ;
Tseng, Chien-Te K. .
JOURNAL OF VIROLOGY, 2015, 89 (07) :3659-3670
[3]  
Alagaili AN, 2014, MBIO, V5, DOI [10.1128/mBio.00884-14, 10.1128/mBio.01482-14]
[4]   Risk Factors for Primary Middle East Respiratory Syndrome Coronavirus Illness in Humans, Saudi Arabia, 2014 [J].
Alraddadi, Basem M. ;
Watson, John T. ;
Almarashi, Abdulatif ;
Abedi, Glen R. ;
Turkistani, Amal ;
Sadran, Musallam ;
Housa, Abeer ;
Almazroa, Mohammad A. ;
Alraihan, Naif ;
Banjar, Ayman ;
Albalawi, Eman ;
Alhindi, Hanan ;
Choudhry, Abdul Jamil ;
Meiman, Jonathan G. ;
Paczkowski, Magdalena ;
Curns, Aaron ;
Mounts, Anthony ;
Feikin, Daniel R. ;
Marano, Nina ;
Swerdlow, David L. ;
Gerber, Susan I. ;
Hajjeh, Rana ;
Madani, Tariq A. .
EMERGING INFECTIOUS DISEASES, 2016, 22 (01) :49-55
[5]   Clinical Assessment of a Novel Recombinant Simian Adenovirus ChAdOx1 as a Vectored Vaccine Expressing Conserved Influenza A Antigens [J].
Antrobus, Richard D. ;
Coughlan, Lynda ;
Berthoud, Tamara K. ;
Dicks, Matthew D. ;
Hill, Adrian V. S. ;
Lambe, Teresa ;
Gilbert, Sarah C. .
MOLECULAR THERAPY, 2014, 22 (03) :668-674
[6]   Evidence for Camel-to-Human Transmission of MERS Coronavirus [J].
Azhar, Esam I. ;
El-Kafrawy, Sherif A. ;
Farraj, Suha A. ;
Hassan, Ahmed M. ;
Al-Saeed, Muneera S. ;
Hashem, Anwar M. ;
Madani, Tariq A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2014, 370 (26) :2499-2505
[7]   Nosocomial Outbreak of Middle East Respiratory Syndrome in a Large Tertiary Care Hospital - Riyadh, Saudi Arabia, 2015 [J].
Balkhy, Hanan H. ;
Alenazi, Thamer H. ;
Alshamrani, Majid M. ;
Baffoe-Bonnie, Henry ;
Al-Abdely, Hail M. ;
El-Saed, Aiman ;
Al Arbash, Hussain A. ;
Al Mayahi, Zayid K. ;
Assiri, Abdullah M. ;
bin Saeed, Abdulaziz .
MMWR-MORBIDITY AND MORTALITY WEEKLY REPORT, 2016, 65 (06) :163-164
[8]   A Double-Inactivated Severe Acute Respiratory Syndrome Coronavirus Vaccine Provides Incomplete Protection in Mice and Induces Increased Eosinophilic Proinflammatory Pulmonary Response [J].
Bolles, Meagan ;
Deming, Damon ;
Long, Kristin ;
Agnihothram, Sudhakar ;
Whitmore, Alan ;
Ferris, Martin ;
Funkhouser, William ;
Gralinski, Lisa ;
Totura, Allison ;
Heise, Mark ;
Baric, Ralph S. .
JOURNAL OF VIROLOGY, 2011, 85 (23) :12201-12215
[9]   Efficacy assessment of a cell-mediated immunity HIV-1 vaccine (the Step Study): a double-blind, randomised, placebo-controlled, test-of-concept trial [J].
Buchbinder, Susan P. ;
Mehrotra, Devon V. ;
Duerr, Ann ;
Fitzgerald, Daniel W. ;
Mogg, Robin ;
Li, David ;
Gilbert, Peter B. ;
Lama, Javier R. ;
Marmor, Michael ;
del Rio, Carlos ;
McElrath, M. Juliana ;
Casimiro, Danilo R. ;
Gottesdiener, Keith M. ;
Chodakewitz, Jeffrey A. ;
Corey, Lawrence ;
Robertson, Michael N. .
LANCET, 2008, 372 (9653) :1881-1893
[10]   Purified coronavirus spike protein nanoparticles induce coronavirus neutralizing antibodies in mice [J].
Coleman, Christopher M. ;
Liu, Ye V. ;
Mu, Haiyan ;
Taylor, Justin K. ;
Massare, Michael ;
Flyer, David C. ;
Glenn, Gregory M. ;
Smith, Gale E. ;
Frieman, Matthew B. .
VACCINE, 2014, 32 (26) :3169-3174