scholarly journals Advancements in DNA vaccine vectors, non-mechanical delivery methods, and molecular adjuvants to increase immunogenicity

2017 ◽  
Vol 13 (12) ◽  
pp. 2837-2848 ◽  
Author(s):  
John J. Suschak ◽  
James A. Williams ◽  
Connie S. Schmaljohn
Vaccines ◽  
2019 ◽  
Vol 7 (2) ◽  
pp. 42 ◽  
Author(s):  
Lumena Louis ◽  
Megan C. Wise ◽  
Hyeree Choi ◽  
Daniel O. Villarreal ◽  
Kar Muthumani ◽  
...  

Identification of novel molecular adjuvants which can boost and enhance vaccine-mediated immunity and provide dose-sparing potential against complex infectious diseases and for immunotherapy in cancer is likely to play a critical role in the next generation of vaccines. Given the number of challenging targets for which no or only partial vaccine options exist, adjuvants that can address some of these concerns are in high demand. Here, we report that a designed truncated Interleukin-36 gamma (IL-36 gamma) encoded plasmid can act as a potent adjuvant for several DNA-encoded vaccine targets including human immunodeficiency virus (HIV), influenza, and Zika in immunization models. We further show that the truncated IL-36 gamma (opt-36γt) plasmid provides improved dose sparing as it boosts immunity to a suboptimal dose of a Zika DNA vaccine, resulting in potent protection against a lethal Zika challenge.


2005 ◽  
Vol 78 (3) ◽  
pp. 647-655 ◽  
Author(s):  
Cevayir Coban ◽  
Ken J. Ishii ◽  
Mayda Gursel ◽  
Dennis M. Klinman ◽  
Nirbhay Kumar

Virology ◽  
2008 ◽  
Vol 375 (1) ◽  
pp. 48-58 ◽  
Author(s):  
Jin Su ◽  
Christy Willert ◽  
Lacrimioara Comanita ◽  
Andrew Peters ◽  
Philippe-Alexandre Gilbert ◽  
...  

Vaccines ◽  
2014 ◽  
Vol 2 (2) ◽  
pp. 196-215 ◽  
Author(s):  
Devon Shedlock ◽  
Colleen Tingey ◽  
Lavanya Mahadevan ◽  
Natalie Hutnick ◽  
Emma Reuschel ◽  
...  

2012 ◽  
Vol 11 (1) ◽  
pp. 107 ◽  
Author(s):  
Diana M Bower ◽  
Kristala LJ Prather

Author(s):  
Rosamund Chapman ◽  
Edward Rybicki

DNA vaccines are stable, safe, cost effective to produce and relatively quick and easy to manufacture. However, to date DNA vaccines have shown relatively poor immunogenicity in humans despite promising preclinical results. Consequently, a number of different approaches have been investigated to improve the immunogenicity of DNA vaccines. These include the use of improved delivery methods, adjuvants, stronger promoters and enhancer elements to increase antigen expression, and codon optimization of the gene of interest. This review describes the creation and use of a DNA vaccine vector containing a porcine circovirus (PCV-1) enhancer element that significantly increases recombinant antigen expression and immunogenicity and allows for dose sparing. A 172bp region containing the PCV-1 capsid protein promoter (Pcap) and a smaller element (PC; 70 bp) within this were found to be equally effective. DNA vaccines containing the Pcap region expressing various HIV-1 antigens were found to be highly immunogenic in mice, rabbits and macaques, at 4 to 10-fold lower doses than normally used and to be highly effective in heterologous prime-boost regimens. By lowering the amount of DNA used for immunization, safety concerns over injecting large amounts of DNA into humans can be overcome.


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