DNA VaccinesMark W. Saltzman, Hong Shen, Janet L. Brandsma Springer Science & Business Media, 2008 M02 2 - 384 pages In the early 1990s, almost 200 yr after Edward Jenner demonstrated the effectiveness of the smallpox vaccine, a new paradigm for vaccination emerged. The conventional method of vaccination required delivery of whole pathogens or structural subunits, but in this new approach, DNA or genetic information was administered to elicit an immunological response. Once it was observed that plasmid DNA delivered in vivo led to production of an encoded transgene (1), two ground-breaking studies demonstrated that immunological responses could be generated against antigenic transgenes via plasmid DNA delivered by DNA vaccination (as this approach is called) (2,3). The appe- ance of this new vaccination strategy coincided with advances in molecular biology, which provided new tools to study and manipulate the basic elements of an organism’s genome and also could also be applied to the design and production of DNA vaccines. DNA Vaccines is a major updated and enhancement of the first edition. It reviews state-of-the-art methods in DNA vaccine technology, with chapters describing DNA vaccine design, delivery systems, adjuvants, current appli- tions, methods of production, and quality control. Consistent with the approach of the Methods in Molecular Medicine series, these chapters contain detailed practical procedures on the latest DNA vaccine technology. The enthusiasm for DNA vaccine technology is made clear by the number of research studies published on this topic since the mid-1990s. |
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Contents
Design of Plasmid DNA Constructs for Vaccines | 11 |
Vaccination With Messenger | 23 |
A Stress ProteinFacilitated Antigen Expression System | 41 |
In Vitro Assay of Immunostimulatory Activities | 55 |
Delivery of DNA Vaccines Using Electroporation | 73 |
A Brief Overview | 83 |
NeedleFree Delivery of Veterinary DNA Vaccines | 91 |
SurfaceModified Biodegradable Microspheres | 107 |
Modifying Professional AntigenPresenting Cells to Enhance | 199 |
ReplicaseBased DNA Vaccines for Allergy Treatment | 221 |
Immunological Responses of Neonates and Infants | 239 |
DNA Vaccines for Allergy Treatment | 253 |
Protection From Autoimmunity by DNA Vaccination | 269 |
The Use of Bone MarrowChimeric Mice in Elucidating | 281 |
DNA VACCINE PRODUCTION PURIFICATION AND QUALITY | 293 |
Production of Plasmid DNA in Industrial Quantities According | 339 |
Subcellular Trafficking Pathways by Indirect | 127 |
DNA VACCINE ADJUVANTS AND ACTIVITY ENHANCEMENT | 137 |
Complexes of DNA Vaccines With Cationic Antigenic Peptides | 159 |
PrimeBoost Strategies in DNA Vaccines | 171 |
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Common terms and phrases
acid activation addition adjuvants allow animals antibody antigen approach assay bacterial buffer CD8+ cells cellular centrifuge chromatography clinical cloning complex concentration Construction containing culture cytokine delivery described detection determine diluted DNA vaccines edited effective efficiency electroporation encoding enhance et al expression filter final g/mL gene growth human immune responses Immunol increase Incubate induce injection levels lysis material medium Methods mice Molecular motifs mRNA Note optimal peptide plasmid DNA plate Prepare presentation priming production protection protein Protocols purification recombinant remove restriction room temperature sample selection sequence solution specific splenocytes staining standard step sterile stimulation Store strategies studies surface T-cell tion tissue transfected transfer tube tumor vector virus vivo volume Wash Western blotting yield