Title: Viruses%20and%20Gene%20Therapy
1Viruses and Gene Therapy
- The good news about viruses
2Quality of viral vector
- Size of insert
- Integration or not/and where
- Ability to obtain in high titer
- Transduction efficiency
- Target cell specificity - pseudotyping
- Expression efficiency/control
- Possible pathogenicity or lack
- No immune response developed
3Useful vectors
- Retroviruses including HIV
- Adenovirus
- Adeno-associated virus (AAV)
- Herpes simplex virus
- Vaccinia virus
- DNA vectors
4Virus Insert size Transduction efficiency Integration Target cells Problems
Retrovirus 8 kb High Yes Dividing cells (pseudo- typed) Insertional mutagenesis
Adeno-virus 30 kb High No Cells w/ receptor Immunity
AAV 4kb High Random or site sp. Cells w/ receptor Small insert size
HSV 40 kb Low No Neurons Latency/ immunity
Vaccinia 25 kb High No Cells w/ receptor Immunity
5Retroviruses
- Require LTR and packaging signal
- LTR modified not to be a promotor
- Cloned gene inserted with strong promotor (pCMV)
and may have IRES - HIV vectors may have some accessory genes if LTR
promotor is used (TAT)
6Created using a packaging cell line
- Genes for gag/pol/env on separate plasmid to get
packaging - May have two or three plasmids for trans genes to
reduce recombination
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8- Advantages
- Stable integration
- Can design to target HIV infected cells with
suicide gene - Can add other promoters that respond only in
specific cells - Disadvantages
- No replication and spread of vector
- Integration may be random
- Requires dividing cell to integrate and express
- What would happen to a retroviral vector with
pCMV and HSV-TK injected into brain tumor and
treatment with ganciclovir? - No affect on neurons so can treat glioma
- TK activates ganciclovir and kills cells
- What would happen if used vector to add WT p53
gene to lung cancer tumor?
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10Adenovirus vectors
- Non-enveloped so no pseudotyping
- Requires elimination of early gene (E1 or E3) and
other nonessential genes and becomes defective - Packaging cell line has E gene integrated and
expressed (less likely crossover) - Gutless vectors have only the inverted terminal
repeats (ITR) and a packaging signal and get all
other gene products in trans in packaging cell
11- Vector-infected cells are removed by immune
system so transient response but that is reduced
in gutless vector - May not work at all if host starts with some Ad
immunity - Infects wide range of cells (common receptors)
12Tumor destruction by adenovirus
- E1B region binds and inactivates p53 protein
- mutant adenovirus (dl1520) that cannot produce
E1B wont reproduce - tumor cells lacking functional p53 can support
replication of this virus
13- C33A lacks p53
- U2OS has p53
- Circles WT
- Squares mutant
14Which side has the Wt? The mutant?
15Tumors in mice after treatment with Wt or mutant
16Adenovirus carries lots of DNA
- Put human hepatitis B genome into ad cloning
vector (removed E1 and E3 genes) - Hep genome also had GFP linked to pCMV as marker
to recognize transduced cells - Used to create HepB cell line in mouse cells that
produces infectious viruses from nonintegrated
DNA - Infected mouse as well - small animal model
- Crossed species barrier
17AAV - parvovirus
- Requires adenovirus early genes to replicate -
not related - ssDNA with promoter and two genes - capsid and
replication protein - Terminal repeats allow for specific integration
into genome if helper is not there - Vector has TR and Promoter - no rep and capsid
insert size is small - W/o rep integration is at random
18- Correcting hemophilia in dogs - AAV vector with
factor IX - Tumor reduction - AAV vector with angiostatin
19HSV vectors come in three varieties
- Recombinant virus made replication deficient w/o
IE gene - Replication conditional replicate in certain cell
lines - Amplicon - bacterial plasmid-based
- Neurotropic but problems with immunity
- Large virus with many nonessential genes - can
add 150KB
20HSV amplicons
- Plasmid contains
- HSV ORI
- HSV packaging signal
- IE promoter and gene of interest
- Selection marker
- Virus made in cell that provides all other
proteins in trans
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