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dc.contributor.editorIsaguliants, Maria
dc.contributor.editorLjungberg, Karl
dc.date.accessioned2022-01-11T13:43:10Z
dc.date.available2022-01-11T13:43:10Z
dc.date.issued2021
dc.identifierONIX_20220111_9783036503004_554
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/76819
dc.description.abstractDNA 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.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::M Medicine and Nursingen_US
dc.subject.classificationthema EDItEUR::M Medicine and Nursing::MB Medicine: general issues::MBN Public health and preventive medicine::MBNS Epidemiology and Medical statisticsen_US
dc.subject.otheralphaviruses
dc.subject.otherlayered RNA/DNA vectors
dc.subject.otherDNA vaccines
dc.subject.otherRNA replicons
dc.subject.otherrecombinant particles
dc.subject.othertumor regression
dc.subject.otherprotection against tumor challenges and infectious agents
dc.subject.otherebola virus disease
dc.subject.otherartificial T-cell antigens
dc.subject.otherDNA vaccine constructs
dc.subject.othercomputer design
dc.subject.othergene expression
dc.subject.otherimmunogenicity
dc.subject.otherDNA vaccine
dc.subject.othermRNA vaccine
dc.subject.otherplasmid DNA
dc.subject.otherin vitro transcribed mRNA
dc.subject.otherimmune responses
dc.subject.otherformulations
dc.subject.otherCytolytic T Lymphocytes
dc.subject.otherantibodies
dc.subject.otherinnate immunity
dc.subject.otheradjuvants
dc.subject.othervaccine delivery
dc.subject.otherplasmid
dc.subject.othercytolytic
dc.subject.otherperforin
dc.subject.otherbicistronic
dc.subject.otherHCV
dc.subject.otherHIV
dc.subject.otherIL-36
dc.subject.otheradjuvant
dc.subject.otherDNA
dc.subject.otherZika
dc.subject.otherEpstein-Barr virus
dc.subject.otherlatent proteins
dc.subject.otherLMP2
dc.subject.otherEBNA1
dc.subject.otherLMP1
dc.subject.otherHIV-1
dc.subject.otherenhancer element
dc.subject.othercircovirus
dc.subject.otherinfluenza
dc.subject.otherimmunization
dc.subject.otherintranasal
dc.subject.otherlipid
dc.subject.otherflagellin
dc.subject.otherBCG
dc.subject.othervaccine
dc.subject.otherrBCG
dc.subject.otherHTI
dc.subject.otherT-cell
dc.subject.otherAIDS
dc.subject.otherclinical trial
dc.subject.othertherapeutic vaccine
dc.subject.otherhepatitis C virus (HCV)
dc.subject.othermesenchymal stem cells (MSC)
dc.subject.othermodified MSC
dc.subject.otherDNA immunization
dc.subject.othernonstructural HCV proteins
dc.subject.otherimmune response
dc.subject.otherHCV vaccine
dc.subject.othermyeloid derived suppressor cells (MDSCs)
dc.subject.othern/a
dc.titleAdvances in DNA Vaccines
dc.typebook
oapen.identifier.doi10.3390/books978-3-0365-0301-1
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0
oapen.relation.isbn9783036503004
oapen.relation.isbn9783036503011
oapen.pages210
oapen.place.publicationBasel, Switzerland


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