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1.
Journal of Forensic Medicine ; (6): 411-413, 2007.
Article in Chinese | WPRIM | ID: wpr-983328

ABSTRACT

OBJECTIVE@#To explore the application of immunofluorescence and sandwich ELISA with double-antibodies in detection of human rabies.@*METHODS@#The cerebrum, cerebellum, brainstem, and hippocampus of four patients died of rabies identified by clinical diagnosis were collected and kept in freezer at -70 degrees C or in formaldehyde solution separately. The rat brain tissue infected by CVS strain of rabies virus was used as a positive control and the brain tissue of a patient died of acute pancreatitis was used as a negative control.@*RESULTS@#Rabies virus was detected in the tissues kept in freezer at -70 degrees C and the positive control but was not detected in the tissues kept in formaldehyde solution and the negative control.@*CONCLUSION@#Immunofluorescence and Sandwich ELISA with double-antibodies could be used in detection of human rabies. The samples should be kept in deep frozen temperature condition instead of in formaldehyde solution.


Subject(s)
Animals , Humans , Rats , Antibodies, Viral/analysis , Brain/virology , Enzyme-Linked Immunosorbent Assay/methods , Fluorescent Antibody Technique/methods , Hippocampus/virology , Rabies/virology , Rabies virus/immunology , Reagent Kits, Diagnostic , Sensitivity and Specificity , Tissue Preservation/methods
2.
Journal of Korean Medical Science ; : 108-111, 2003.
Article in English | WPRIM | ID: wpr-63344

ABSTRACT

The delivery of transgenes to the central nervous system (CNS) can be a valuable tool to treat CNS diseases. Various systems for the delivery to the CNS have been developed; vascular delivery of viral vectors being most recent. Here, we investigated gene transfer to the CNS by intravenous injection of recombinant adenoviral vectors, containing green fluorescence protein (GFP) as a reporter gene. Expression of GFP was first observed 6 days after the gene transfer, peaked at 14 days, and almost diminished after 28 days. The observed expression of GFP in the CNS was highly localized to hippocampal CA regions of cerebral neocortex, inferior colliculus of midbrain, and granular cell and Purkinje cell layers of cerebellum. It is concluded that intravenous delivery of adenoviral vectors can be used for gene delivery to the CNS, and hence the technique could be beneficial to gene therapy.


Subject(s)
Animals , Female , Mice , Adenoviruses, Human/isolation & purification , Blood-Brain Barrier , Brain/virology , Cerebellum/cytology , Cerebellum/virology , Comparative Study , Genes, Reporter , Genetic Vectors/administration & dosage , Genetic Vectors/isolation & purification , Genetic Vectors/pharmacokinetics , Hippocampus/virology , Inferior Colliculi/virology , Injections, Intravenous , Luminescent Proteins/analysis , Luminescent Proteins/biosynthesis , Luminescent Proteins/genetics , Mice, Inbred BALB C , Neuroglia/virology , Neurons/virology , Purkinje Cells/virology , Pyramidal Cells/virology , Recombinant Fusion Proteins/analysis , Recombinant Fusion Proteins/biosynthesis , Recombinant Fusion Proteins/genetics , Tail/blood supply , Tissue Distribution
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