Gene Therapy of Cancer pp 305-310 | Cite as
A DNA Vaccine against Malignant Melanoma Coexpressing Antigen and Cytokine
Abstract
Inoculation of plasmid DNA vectors encoding immunogenic proteins induce both, humoral and cell-mediated responses. Protection against challenge with pathogens has provided protective immunity in several cases in animal models. The first demonstration of the protective efficacy of a DNA vaccine in an animal model was reported only four years ago with Influenza A DNA[1]. Since then preclinical studies have been performed with a variety of disease targets such as HIV, bovine herpes virus, Hepatitis B, Hepatitis C virus, rabies, measles, malaria, Herpes simplex virus, papilloma virus, lymphocytic choriomeningitis virus and flavi virus etc. [for review, see 2, 3]. DNA vaccines offer the advantage of stimulating the generation of cytotoxic T lymphocytes (CTLs) against epitopes from a conserved protein of a virus, e.g. the nucleoprotein NP of influenza virus, thereby providing cross-strain protection in a mouse model [1]. From human genetic diseases it is known that individuals lacking antibody response cope rather well with viral infections—but show increased sensitivities to various bacterial pathogens, while T-cell deficiency frequently leads to higher susceptibility to viruses [2].
Keywords
Internal Ribosomal Entry Site Encephalomyocarditis Virus Bovine Growth Hormone Lymphocytic Choriomeningitis Virus Rabies Virus GlycoproteinAbbreviations
- APC
antigen presenting cells
- BGH
bovine growth hormone
- CEA
carcinoembrionic antigen
- CMV
cytomegalovirus
- CTL
cytotoxic lymphocytes
- ELISA
enzyme linked immune absorbance assay
- EMCV
encephalomyocarditis virus
- FDA
Federal Drug administration
- GM-CSF
granulocytemacrophage stimulating factor
- HA
hemagglutinin
- HIV
human immunodeficiency virus
- IRES
internal ribosomal entry site
- LTR
long terminal repeat
- MAGE
melanoma associated antigen
- MHC
major histocompatibility antigen
- NP
nucleoprotein
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References
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