Advances in DNA Vaccines

DNA is a rapidly developing vaccine platform for cancer and infectious and non-infectious diseases. Plasmids are used as immunogens to encode proteins to be further synthesized in vaccine recipients. DNA is mainly synthetic, ensuring enhanced expression in the cells of vaccine recipients (mostly mam...

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Julkaistu: MDPI - Multidisciplinary Digital Publishing Institute 2022
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collection Directory of Open Access Books
description DNA is a rapidly developing vaccine platform for cancer and infectious and non-infectious diseases. Plasmids are used as immunogens to encode proteins to be further synthesized in vaccine recipients. DNA is mainly synthetic, ensuring enhanced expression in the cells of vaccine recipients (mostly mammalians). Their introduction into the host induces antibody and cellular responses. The latter are often more pronounced, and mimic the events occurring in infection, especially viral. There are a few distinct ways in which the vaccine antigen can be processed and presented, which determine the resulting immune response and which can be manipulated. Routinely, the antigen synthesized within the host cell is processed by proteasome, loaded onto, and presented in a complex with MHC I molecules. Processing can be re-routed to the lysosome, or immunogen can be secreted for further presentation in a complex with MHC II. Apart from expression, vaccination efficacy depends on DNA delivery. DNA immunogens are generally administered by intramuscular or intradermal injections, usually followed by electroporation, which enhances delivery 1000-fold. Other techniques are also used, such as noninvasive introduction by biojectors, skin applications with plasters and microneedles/chips, sonication, magnetofection, and even tattooing. An intense debate regarding the pros and cons of different routes of delivery is ongoing. A number of studies have compared the effect of delivery methods at the level of immunogen expression, and the magnitude and specificity of the resulting immune response. According to some, the delivery route determines immunogenic performance; according to others, it can modulate the level of response, but not its specificity or polarity. The progress of research aiming at the optimization of DNA vaccine design, delivery, and immunogenic performance has led to a marked increase in their efficacy in large species and humans. New DNA vaccines for use in the treatment of infectious diseases, cancer, allergies, and autoimmunity are forthcoming. This Special Issue covers various aspects of DNA vaccine development.
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spelling doab-20.500.12854ir-768192024-03-31T13:10:30Z Advances in DNA Vaccines Isaguliants, Maria Ljungberg, Karl alphaviruses layered RNA/DNA vectors DNA vaccines RNA replicons recombinant particles tumor regression protection against tumor challenges and infectious agents ebola virus disease artificial T-cell antigens DNA vaccine constructs computer design gene expression immunogenicity DNA vaccine mRNA vaccine plasmid DNA in vitro transcribed mRNA immune responses formulations Cytolytic T Lymphocytes antibodies innate immunity adjuvants vaccine delivery plasmid cytolytic perforin bicistronic HCV HIV IL-36 adjuvant DNA Zika Epstein-Barr virus latent proteins LMP2 EBNA1 LMP1 HIV-1 enhancer element circovirus influenza immunization intranasal lipid flagellin BCG vaccine rBCG HTI T-cell AIDS clinical trial therapeutic vaccine hepatitis C virus (HCV) mesenchymal stem cells (MSC) modified MSC DNA immunization nonstructural HCV proteins immune response HCV vaccine myeloid derived suppressor cells (MDSCs) n/a thema EDItEUR::M Medicine and Nursing thema EDItEUR::M Medicine and Nursing::MB Medicine: general issues::MBN Public health and preventive medicine::MBNS Epidemiology and Medical statistics DNA is a rapidly developing vaccine platform for cancer and infectious and non-infectious diseases. Plasmids are used as immunogens to encode proteins to be further synthesized in vaccine recipients. DNA is mainly synthetic, ensuring enhanced expression in the cells of vaccine recipients (mostly mammalians). Their introduction into the host induces antibody and cellular responses. The latter are often more pronounced, and mimic the events occurring in infection, especially viral. There are a few distinct ways in which the vaccine antigen can be processed and presented, which determine the resulting immune response and which can be manipulated. Routinely, the antigen synthesized within the host cell is processed by proteasome, loaded onto, and presented in a complex with MHC I molecules. Processing can be re-routed to the lysosome, or immunogen can be secreted for further presentation in a complex with MHC II. Apart from expression, vaccination efficacy depends on DNA delivery. DNA immunogens are generally administered by intramuscular or intradermal injections, usually followed by electroporation, which enhances delivery 1000-fold. Other techniques are also used, such as noninvasive introduction by biojectors, skin applications with plasters and microneedles/chips, sonication, magnetofection, and even tattooing. An intense debate regarding the pros and cons of different routes of delivery is ongoing. A number of studies have compared the effect of delivery methods at the level of immunogen expression, and the magnitude and specificity of the resulting immune response. According to some, the delivery route determines immunogenic performance; according to others, it can modulate the level of response, but not its specificity or polarity. The progress of research aiming at the optimization of DNA vaccine design, delivery, and immunogenic performance has led to a marked increase in their efficacy in large species and humans. New DNA vaccines for use in the treatment of infectious diseases, cancer, allergies, and autoimmunity are forthcoming. This Special Issue covers various aspects of DNA vaccine development. 2022-01-11T13:43:10Z 2022-01-11T13:43:10Z 2021 book ONIX_20220111_9783036503004_554 9783036503004 9783036503011 https://directory.doabooks.org/handle/20.500.12854/76819 eng image/jpeg Attribution 4.0 International https://mdpi.com/books/pdfview/book/4268 https://mdpi.com/books/pdfview/book/4268 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-0365-0301-1 10.3390/books978-3-0365-0301-1 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783036503004 9783036503011 210 Basel, Switzerland open access
spellingShingle alphaviruses
layered RNA/DNA vectors
DNA vaccines
RNA replicons
recombinant particles
tumor regression
protection against tumor challenges and infectious agents
ebola virus disease
artificial T-cell antigens
DNA vaccine constructs
computer design
gene expression
immunogenicity
DNA vaccine
mRNA vaccine
plasmid DNA
in vitro transcribed mRNA
immune responses
formulations
Cytolytic T Lymphocytes
antibodies
innate immunity
adjuvants
vaccine delivery
plasmid
cytolytic
perforin
bicistronic
HCV
HIV
IL-36
adjuvant
DNA
Zika
Epstein-Barr virus
latent proteins
LMP2
EBNA1
LMP1
HIV-1
enhancer element
circovirus
influenza
immunization
intranasal
lipid
flagellin
BCG
vaccine
rBCG
HTI
T-cell
AIDS
clinical trial
therapeutic vaccine
hepatitis C virus (HCV)
mesenchymal stem cells (MSC)
modified MSC
DNA immunization
nonstructural HCV proteins
immune response
HCV vaccine
myeloid derived suppressor cells (MDSCs)
n/a
thema EDItEUR::M Medicine and Nursing
thema EDItEUR::M Medicine and Nursing::MB Medicine: general issues::MBN Public health and preventive medicine::MBNS Epidemiology and Medical statistics
Advances in DNA Vaccines
title Advances in DNA Vaccines
title_full Advances in DNA Vaccines
title_fullStr Advances in DNA Vaccines
title_full_unstemmed Advances in DNA Vaccines
title_short Advances in DNA Vaccines
title_sort advances in dna vaccines
topic alphaviruses
layered RNA/DNA vectors
DNA vaccines
RNA replicons
recombinant particles
tumor regression
protection against tumor challenges and infectious agents
ebola virus disease
artificial T-cell antigens
DNA vaccine constructs
computer design
gene expression
immunogenicity
DNA vaccine
mRNA vaccine
plasmid DNA
in vitro transcribed mRNA
immune responses
formulations
Cytolytic T Lymphocytes
antibodies
innate immunity
adjuvants
vaccine delivery
plasmid
cytolytic
perforin
bicistronic
HCV
HIV
IL-36
adjuvant
DNA
Zika
Epstein-Barr virus
latent proteins
LMP2
EBNA1
LMP1
HIV-1
enhancer element
circovirus
influenza
immunization
intranasal
lipid
flagellin
BCG
vaccine
rBCG
HTI
T-cell
AIDS
clinical trial
therapeutic vaccine
hepatitis C virus (HCV)
mesenchymal stem cells (MSC)
modified MSC
DNA immunization
nonstructural HCV proteins
immune response
HCV vaccine
myeloid derived suppressor cells (MDSCs)
n/a
thema EDItEUR::M Medicine and Nursing
thema EDItEUR::M Medicine and Nursing::MB Medicine: general issues::MBN Public health and preventive medicine::MBNS Epidemiology and Medical statistics
topic_facet alphaviruses
layered RNA/DNA vectors
DNA vaccines
RNA replicons
recombinant particles
tumor regression
protection against tumor challenges and infectious agents
ebola virus disease
artificial T-cell antigens
DNA vaccine constructs
computer design
gene expression
immunogenicity
DNA vaccine
mRNA vaccine
plasmid DNA
in vitro transcribed mRNA
immune responses
formulations
Cytolytic T Lymphocytes
antibodies
innate immunity
adjuvants
vaccine delivery
plasmid
cytolytic
perforin
bicistronic
HCV
HIV
IL-36
adjuvant
DNA
Zika
Epstein-Barr virus
latent proteins
LMP2
EBNA1
LMP1
HIV-1
enhancer element
circovirus
influenza
immunization
intranasal
lipid
flagellin
BCG
vaccine
rBCG
HTI
T-cell
AIDS
clinical trial
therapeutic vaccine
hepatitis C virus (HCV)
mesenchymal stem cells (MSC)
modified MSC
DNA immunization
nonstructural HCV proteins
immune response
HCV vaccine
myeloid derived suppressor cells (MDSCs)
n/a
thema EDItEUR::M Medicine and Nursing
thema EDItEUR::M Medicine and Nursing::MB Medicine: general issues::MBN Public health and preventive medicine::MBNS Epidemiology and Medical statistics
url ONIX_20220111_9783036503004_554