Bacteriophage T4 as a Protein-Based, Adjuvant- and Needle-Free, Mucosal Pandemic Vaccine Design Platform

被引:3
作者
Zhu, Jingen [1 ]
Tao, Pan [2 ]
Chopra, Ashok K. [3 ,4 ]
Rao, Venigalla B. [1 ]
机构
[1] Catholic Univ Amer, Bacteriophage Med Res Ctr, Dept Biol, Washington, DC 20064 USA
[2] Huazhong Agr Univ, Coll Vet Med, State Key Lab Agr Microbiol, Wuhan, Hubei, Peoples R China
[3] Univ Texas Med Branch, Sealy Inst Vaccine Sci, Inst Human Infect & Immun, Dept Microbiol & Immunol, Galveston, TX USA
[4] Univ Texas Med Branch, Galveston Natl Lab, Galveston, TX USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
bacteriophage T4 assembly; CRISPR engineering; pandemic vaccine design; broad humoral immunity; cellular immunity; mucosal immunity; needle- and adjuvant-free intranasal vaccines; OUTER CAPSID PROTEIN; ADAPTIVE IMMUNITY; FOREIGN PROTEINS; PHAGE THERAPY; IN-VITRO; DNA; DISPLAY; DELIVERY; INNATE; BINDING;
D O I
10.1146/annurev-virology-111821-111145
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The COVID-19 pandemic has transformed vaccinology. Rapid deployment of mRNA vaccines has saved countless lives. However, these platforms have inherent limitations including lack of durability of immune responses and mucosal immunity, high cost, and thermal instability. These and uncertainties about the nature of future pandemics underscore the need for exploring next-generation vaccine platforms. Here, we present a novel protein-based, bacteriophage T4 platform for rapid design of efficacious vaccines against bacterial and viral pathogens. Full-length antigens can be displayed at high density on a 120 x 86 nm phage capsid through nonessential capsid binding proteins Soc and Hoc. Such nanoparticles, without any adjuvant, induce robust humoral, cellular, and mucosal responses when administered intranasally and confer sterilizing immunity. Combined with structural stability and ease of manufacture, T4 phage provides an excellent needle-free, mucosal pandemic vaccine platform and allows equitable vaccine access to low- and middle-income communities across the globe.
引用
收藏
页码:395 / 420
页数:26
相关论文
共 143 条
[1]   COVID-19 vaccination: The road ahead [J].
Altmann, Daniel M. ;
Boyton, Rosemary J. .
SCIENCE, 2022, 375 (6585) :1127-1132
[2]   Intranasal COVID-19 vaccines: From bench to bed [J].
Alu, Aqu ;
Chen, Li ;
Lei, Hong ;
Wei, Yuquan ;
Tian, Xiaohe ;
Wei, Xiawei .
EBIOMEDICINE, 2022, 76
[3]   Vaccine delivery: a matter of size, geometry, kinetics and molecular patterns [J].
Bachmann, Martin F. ;
Jennings, Gary T. .
NATURE REVIEWS IMMUNOLOGY, 2010, 10 (11) :787-796
[4]   The biology of mucus: Composition, synthesis and organization [J].
Bansil, Rama ;
Turner, Bradley S. .
ADVANCED DRUG DELIVERY REVIEWS, 2018, 124 :3-15
[5]   Phage-based vaccines [J].
Bao, Qing ;
Li, Xiang ;
Han, Gaorong ;
Zhu, Ye ;
Mao, Chuanbin ;
Yang, Mingying .
ADVANCED DRUG DELIVERY REVIEWS, 2019, 145 :40-56
[6]   Bacteriophage adhering to mucus provide a non-host-derived immunity [J].
Barr, Jeremy J. ;
Auro, Rita ;
Furlan, Mike ;
Whiteson, Katrine L. ;
Erb, Marcella L. ;
Pogliano, Joe ;
Stotland, Aleksandr ;
Wolkowicz, Roland ;
Cutting, Andrew S. ;
Doran, Kelly S. ;
Salamon, Peter ;
Youle, Merry ;
Rohwer, Forest .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (26) :10771-10776
[7]   The biology of influenza viruses [J].
Bouvier, Nicole M. ;
Palese, Peter .
VACCINE, 2008, 26 :D49-D53
[8]   IgA Responses to Microbiota [J].
Bunker, Jeffrey J. ;
Bendelac, Albert .
IMMUNITY, 2018, 49 (02) :211-224
[9]   Monomeric streptavidin phage display allows efficient immobilization of bacteriophages on magnetic particles for the capture, separation, and detection of bacteria [J].
Carmody, Caitlin M. ;
Nugen, Sam R. .
SCIENTIFIC REPORTS, 2023, 13 (01)
[10]   Immunogenicity of bacteriophages [J].
Champagne-Jorgensen, Kevin ;
Luong, Tiffany ;
Darby, Taylor ;
Roach, Dwayne R. .
TRENDS IN MICROBIOLOGY, 2023, 31 (10) :1058-1071