Protection against tuberculosis by a single intranasal administration of DNA-hsp65 vaccine complexed with cationic liposomes
Open Access
- 22 July 2008
- journal article
- research article
- Published by Springer Nature in BMC Immunology
- Vol. 9 (1) , 1-13
- https://doi.org/10.1186/1471-2172-9-38
Abstract
Background: The greatest challenges in vaccine development include optimization of DNA vaccines for use in humans, creation of effective single-dose vaccines, development of delivery systems that do not involve live viruses, and the identification of effective new adjuvants. Herein, we describe a novel, simple technique for efficiently vaccinating mice against tuberculosis (TB). Our technique consists of a single-dose, genetic vaccine formulation of DNA-hsp65 complexed with cationic liposomes and administered intranasally.Results: We developed a novel and non-toxic formulation of cationic liposomes, in which the DNA-hsp65 vaccine was entrapped (ENTR-hsp65) or complexed (COMP-hsp65), and used to immunize mice by intramuscular or intranasal routes. Although both liposome formulations induced a typical Th1 pattern of immune response, the intramuscular route of delivery did not reduce the number of bacilli. However, a single intranasal immunization with COMP-hsp65, carrying as few as 25 μg of plasmid DNA, leads to a remarkable reduction of the amount of bacilli in lungs. These effects were accompanied by increasing levels of IFN-γ and lung parenchyma preservation, results similar to those found in mice vaccinated intramuscularly four times with naked DNA-hsp65 (total of 400 μg).Conclusion: Our objective was to overcome the significant obstacles currently facing DNA vaccine development. Our results in the mouse TB model showed that a single intranasal dose of COMP-hsp65 elicited a cellular immune response that was as strong as that induced by four intramuscular doses of naked-DNA. This formulation allowed a 16-fold reduction in the amount of DNA administered. Moreover, we demonstrated that this vaccine is safe, biocompatible, stable, and easily manufactured at a low cost. We believe that this strategy can be applied to human vaccines to TB in a single dose or in prime-boost protocols, leading to a tremendous impact on the control of this infectious disease.Keywords
This publication has 57 references indexed in Scilit:
- Increased levels of interferon‐γ primed by culture filtrate proteins antigen and CpG‐ODN immunization do not confer significant protection against Mycobacterium tuberculosis infectionImmunology, 2007
- Evaluation of a novel vaccine (HVJ–liposome/HSP65 DNA + IL-12 DNA) against tuberculosis using the cynomolgus monkey model of TBVaccine, 2007
- Gene-based vaccines: recent technical and clinical advancesTrends in Molecular Medicine, 2006
- Therapeutic cancer vaccinesCurrent Opinion in Immunology, 2006
- Phase I clinical trial safety of DNA- and modified virus Ankara-vectored human immunodeficiency virus type 1 (HIV-1) vaccines administered alone and in a prime-boost regime to healthy HIV-1-uninfected volunteersVaccine, 2006
- Biodegradable mucoadhesive particulates for nasal and pulmonary antigen and DNA deliveryAdvanced Drug Delivery Reviews, 2005
- Liposomes and ISCOMS as vaccine formulationsBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1995
- Heterologous Protection Against Influenza by Injection of DNA Encoding a Viral ProteinScience, 1993
- Immunological adjuvants: a role for liposomesImmunology Today, 1990
- Diffusion of univalent ions across the lamellae of swollen phospholipidsJournal of Molecular Biology, 1965