Baculovirus as vectors for human cells and applications in organ transplantation

[Display omitted] ► We discuss baculoviruses as vectors for gene therapy in ischemia reperfusion injury (IRI). ► We test different models of IRI in vitro. ► Baculovirus concentration methods are also compared and the addition of PEG is described. ► Using baculovirus for transduction of solid organs...

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Published inJournal of invertebrate pathology Vol. 107; pp. S49 - S58
Main Authors Hitchman, Richard B, Murguía-Meca, Fernanda, Locanto, Elisabetta, Danquah, John, King, Linda A.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.07.2011
Subjects
AcMNPV
adaptive immunity
Autographa californica
Autographa californica multiple nucleopolyhedrovirus
Baculovirus
Cells, Cultured
Data processing
Gene Expression Regulation, Viral
Gene therapy
gene transfer
Gene Transfer Techniques
genes
Genetic Therapy - methods
Genetic Vectors
Humans
ischemia
Ischemia reperfusion injury
kidney cells
liver
Nucleopolyhedrovirus - genetics
Organ Transplantation
Reperfusion Injury - genetics
Reperfusion Injury - therapy
RT-PCR profiler array
viruses
AcMNPV
Organ transplantation
Ischemia reperfusion injury
Baculovirus
Gene therapy
RT-PCR profiler array
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Abstract [Display omitted] ► We discuss baculoviruses as vectors for gene therapy in ischemia reperfusion injury (IRI). ► We test different models of IRI in vitro. ► Baculovirus concentration methods are also compared and the addition of PEG is described. ► Using baculovirus for transduction of solid organs is then detailed. ► Finally we determine baculovirus gene expression profiles in cells using RT-QPCR arrays. The baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is able to transduce a wide range of mammalian cells and shows preferential uptake in some, particularly liver and kidney cells. This suggests that the virus may be useful for delivery of protective genes for ameliorating the effects of ischaemia reperfusion injury (IRI) in solid organs during transplantation procedures. In this chapter we discuss the advantages of the baculovirus over other virus vectors for gene delivery in organ transplantation and describe some of the protective genes which may be used to ameliorate the effects of IRI. We then describe a method for concentrating baculovirus for use in an ex vivo transduction model. Data are also provided for the effects of virus transduction in vitro on the innate and adaptive immune response. We conclude with a discussion on the future considerations for using baculovirus for delivery and expression of protective genes in organ transplantation.
AbstractList The baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is able to transduce a wide range of mammalian cells and shows preferential uptake in some, particularly liver and kidney cells. This suggests that the virus may be useful for delivery of protective genes for ameliorating the effects of ischaemia reperfusion injury (IRI) in solid organs during transplantation procedures. In this chapter we discuss the advantages of the baculovirus over other virus vectors for gene delivery in organ transplantation and describe some of the protective genes which may be used to ameliorate the effects of IRI. We then describe a method for concentrating baculovirus for use in an ex vivo transduction model. Data are also provided for the effects of virus transduction in vitro on the innate and adaptive immune response. We conclude with a discussion on the future considerations for using baculovirus for delivery and expression of protective genes in organ transplantation.
[Display omitted] ► We discuss baculoviruses as vectors for gene therapy in ischemia reperfusion injury (IRI). ► We test different models of IRI in vitro. ► Baculovirus concentration methods are also compared and the addition of PEG is described. ► Using baculovirus for transduction of solid organs is then detailed. ► Finally we determine baculovirus gene expression profiles in cells using RT-QPCR arrays. The baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is able to transduce a wide range of mammalian cells and shows preferential uptake in some, particularly liver and kidney cells. This suggests that the virus may be useful for delivery of protective genes for ameliorating the effects of ischaemia reperfusion injury (IRI) in solid organs during transplantation procedures. In this chapter we discuss the advantages of the baculovirus over other virus vectors for gene delivery in organ transplantation and describe some of the protective genes which may be used to ameliorate the effects of IRI. We then describe a method for concentrating baculovirus for use in an ex vivo transduction model. Data are also provided for the effects of virus transduction in vitro on the innate and adaptive immune response. We conclude with a discussion on the future considerations for using baculovirus for delivery and expression of protective genes in organ transplantation.
Author Murguía-Meca, Fernanda
Danquah, John
King, Linda A.
Hitchman, Richard B
Locanto, Elisabetta
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Keywords AcMNPV
Organ transplantation
Ischemia reperfusion injury
Baculovirus
Gene therapy
RT-PCR profiler array
Language English
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Snippet [Display omitted] ► We discuss baculoviruses as vectors for gene therapy in ischemia reperfusion injury (IRI). ► We test different models of IRI in vitro. ►...
The baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is able to transduce a wide range of mammalian cells and shows preferential...
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SubjectTerms AcMNPV
adaptive immunity
Autographa californica
Autographa californica multiple nucleopolyhedrovirus
Baculovirus
Cells, Cultured
Data processing
Gene Expression Regulation, Viral
Gene therapy
gene transfer
Gene Transfer Techniques
genes
Genetic Therapy - methods
Genetic Vectors
Humans
ischemia
Ischemia reperfusion injury
kidney cells
liver
Nucleopolyhedrovirus - genetics
Organ Transplantation
Reperfusion Injury - genetics
Reperfusion Injury - therapy
RT-PCR profiler array
viruses
Title Baculovirus as vectors for human cells and applications in organ transplantation
URI https://dx.doi.org/10.1016/j.jip.2011.05.005
https://www.ncbi.nlm.nih.gov/pubmed/21784231
https://search.proquest.com/docview/880998087
https://search.proquest.com/docview/888095818
Volume 107
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