A Novel Molecular Design for a Hybrid Phage-Dna Construct Against Dkk1 Publisher Pubmed



Khalili S^{1, 2} ; Rasaee MJ² ; Bamdad T³ ; Mardsoltani M⁴ ; Asadi Ghalehni M⁵ ; Jahangiri A⁶ ; Pouriayevali MH⁷ ; Aghasadeghi MR⁷ ; Malaei F² Show Affiliations
Source: Molecular Biotechnology Published:2018

Abstract

Nucleic acid immunization has recently exhibited a great promise for immunotherapy of various diseases. However, it is now clear that powerful strategies are imminently needed to improve their efficiency. In this regard, whole bacteriophage particles have been described as efficient DNA vaccine delivery vehicles, capable of circumventing the limitations of naked DNA immunization. Moreover, phage particles could be engineered to display specific peptides on their surfaces. Given these inherent characteristics of phages, we have designed a novel hybrid phage-DNA immunization vector using both M13 and pAAV plasmid elements. Following the construction and in vitro confirmation of the designed vectors, they were used for comparative mice immunization, carrying the same DNA sequence. The results indicated the efficacy of the designed hybrid phage particles, to elicit higher humoral immunity, in comparison to conventional DNA-immunization vectors (pCI). In light of these findings, it could be concluded that using adeno-associated virus (AAV) expression cassette along with displaying TAT peptide on the surface of the phage particle could be deemed as an appealing strategy to enhance the DNA-immunization and vaccination efficacy. © 2018, Springer Science+Business Media, LLC, part of Springer Nature.