A Bacteriophage T4 Nanoparticle-Based Dual Vaccine against Anthrax and Plague

mBio - Tập 9 Số 5 - 2018
Tao Pan1, Marthandan Mahalingam1, Jingen Zhu1, Mahtab Moayeri2, Jian Sha3,4, William S. Lawrence3,4, Stephen H. Leppla2, Ashok K. Chopra5,3,4,6,7, Venigalla B. Rao1
1Department of Biology, The Catholic University of America, Washington, DC, USA,
2Microbial Pathogenesis Section, Laboratory of Parasitic Diseases, NIAID, NIH, Bethesda, Maryland, USA
3Department of Microbiology and Immunology, University of Texas Medical Branch Galveston, Texas USA
4Galveston National Laboratory, University of Texas Medical Branch, Galveston, Texas, USA
5Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch, Galveston, Texas, USA
6Institute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, Texas, USA
7Sealy Institute for Vaccine Sciences, University of Texas Medical Branch, Galveston, Texas, USA

Tóm tắt

Following the deadly anthrax attacks of 2001, the Centers for Disease Control and Prevention (CDC) determined that Bacillus anthracis and Yersinia pestis that cause anthrax and plague, respectively, are two Tier 1 select agents that pose the greatest threat to the national security of the United States. Both cause rapid death, in 3 to 6 days, of exposed individuals. We engineered a virus nanoparticle vaccine using bacteriophage T4 by incorporating key antigens of both B. anthracis and Y. pestis into one formulation. Two doses of this vaccine provided complete protection against both inhalational anthrax and pneumonic plague in animal models. This dual anthrax-plague vaccine is a strong candidate for stockpiling against a potential bioterror attack involving either one or both of these biothreat agents. Further, our results establish the T4 nanoparticle as a novel platform to develop multivalent vaccines against pathogens of high public health significance.

Từ khóa


Tài liệu tham khảo

10.1073/pnas.1402981111

Centers for Disease Control and Prevention. 2017. Bioterrorism agents/diseases. Centers for Disease Control and Prevention Atlanta GA. https://emergency.cdc.gov/agent/agentlist-category.asp. Accessed 17 August 2017.

10.1001/jama.287.17.2236

10.1001/jama.283.17.2281

10.1172/JCI0216204

10.3389/fmicb.2015.01009

10.1038/nature02763

10.1007/s00253-011-3380-6

10.1586/14760584.7.2.209

10.2174/1389201014666131226122243

10.1016/j.vaccine.2015.11.025

10.1016/j.bcp.2016.05.001

10.1093/infdis/jiu648

10.1111/j.1574-695X.1995.tb00196.x

10.1016/S0264-410X(98)80110-2

10.1371/journal.ppat.1003495

10.1586/14760584.2013.814860

10.3389/fimmu.2017.00687

10.1002/jps.23422

10.1128/CVI.00174-12

10.1016/j.immuni.2010.10.002

10.1016/j.cell.2012.02.012

10.1016/j.addr.2016.09.009

10.1016/j.addr.2014.10.023

10.1586/erv.10.115

10.1089/vim.2009.0017

10.1021/bm5011646

Tao P, Zhu J, Mahalingam M, Batra H, Rao VB. 2018. Bacteriophage T4 nanoparticles for vaccine delivery against infectious diseases. Adv Drug Deliv Rev

10.3390/ijms13045179

10.1073/pnas.1708483114

10.1073/pnas.0400444101

10.1128/IAI.73.11.7304-7310.2005

10.1016/j.jmb.2009.10.007

10.1016/j.jmb.2007.05.008

10.1128/CVI.05376-11

10.1016/j.vaccine.2010.11.049

10.1128/CVI.00150-16

10.1016/j.micpath.2012.09.011

10.1016/j.micinf.2008.11.009

10.1128/IAI.00269-13

10.1073/pnas.1300867110

10.1371/journal.pone.0112802

10.1177/0300985810378112

Zaucha GM, Pitt LM, Estep J, Ivins BE, Friedlander AM. 1998. The pathology of experimental anthrax in rabbits exposed by inhalation and subcutaneous inoculation. Arch Pathol Lab Med 122:982–992.

10.1128/mBio.01356-17

National Research Council. 2011. Guide for the care and use of laboratory animals, 8th ed. National Academies Press, Washington, DC.

10.1007/978-1-4939-3387-7_28

10.1007/978-1-4939-6869-5_15

10.1021/acssynbio.7b00179

10.1126/sciadv.aar4134

10.1002/jps.22267

10.1073/pnas.0906581106