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Many strategies for redirecting the tropism of murine Moloney leukemia virus (MMLV) have been described. Preformed virion-liposome complexes, termed virosomes, have been reported to be relatively stable. Virosomes mediate envelope-independent transduction that allows efficient superinfection of resistant cell lines; however, virosome-mediated transduction behaves in a non–target-specific manner. We developed a novel method using antibodies to direct MMLV to vascular endothelium. We have given the term immunovirosomes to the complexes formed between viruses, liposomes, and antibodies. These immunovirosomes improve the transduction efficiency of the viruses and alter their tropism. We have shown improved transduction when immunovirosomes were targeted at the endocytic receptors CD71 and CD62E/P and rather less good delivery when targeted at CD106. The enhancement of the transduction efficiency was transient, however, suggesting that rerouting the entry pathway of viruses alters the expression properties of the viruses.
Viral and nonviral vectors can be manipulated to increase the efficiency and specificity for vascular cell transduction (1,2). This can be achieved either by modifying the cell binding properties of the vectors or by the use of cell-selective promoters (3,4). Altering the tropism of viral vectors can be achieved by genetic modification of the viral envelope (5–8) or by the use of proteins derived from other enveloped viruses (9,10). Alternatively, targeting molecules can be derived from nonretroviral proteins expressed on the packaging cell line (11–13). A further alternative is to use adaptor molecules that retarget the virus to specific cell-surface molecules (14–16). These approaches can be time consuming and often affect the production of the virus. In addition, although in some cases they offer high specificity, they can result in poor transduction efficiency.
In this report, we describe an alternative targeting strategy using immunovirosomes generated by mixing mildly aggregated monoclonal antibodies, liposomes, and viral particles. This strategy is based on the ability of cationic liposomes to form stable complexes with viral vectors (17,18). This interaction has been reported for Moloney murine leukemia virus (MMLV). Here, we have shown that immunovirosomes carrying monoclonal antibodies against endothelial markers can target activated vascular endothelium. The resulting gene transfer efficiency is enhanced if endocytic receptors are chosen. Importantly, our results demonstrate that changing viral tropism can alter the ability of viral transduction to result in long-term expression. These findings will have profound consequences on future viral vector design with respect to improving specificity and efficiency.
RPMI-1640, CD hybridoma medium, hybridoma serum-free medium (SFM), human endothelial basal growth-SFM, l-glutamine, penicillin, streptomycin, and trypsin-EDTA were purchased from Invitrogen (Paisley, UK), and fetal calf serum (FCS) was purchased from Globepharm (Esher, UK). The synthetic liposome Tfx-50 was purchased from Promega (Southampton, UK). Lipofectin and LipofectAMINE were obtained from Invitrogen. Other reagents were purchased from Sigma (Poole, UK), unless stated otherwise.
Hybridomas producing the anti-human transferrin receptor (CD71) mAb, OKT9; anti-E/P-selectin (CD62E/P), 1.2B6 (dual-specificity), and anti-VCAM-1 (CD106), 1.4C3, were grown and purified by protein G chromatography, as described (19).
Immunoliposomes were prepared as described (19,20). In brief, heat-aggregated Ab [optimal mAb concentrations; OKT9 (60 μ g/mL), 1.2B6 (30 μ g/mL), and 1.4C3 (60 μ g/mL)] was mixed with liposomes (Tfx-50, Lipofectin, or LipofectAMINE), for 30 min at room temperature (in total volume of 250 μ L in Opti-MEM). For plasmid-mediated transfection, the immunoliposomes were then incubated with DNA at a ratio recommended by the manufacturer for the liposome-DNA complex. The resulting transfection complexes were added to endothelial cells (ECs). As in the case of the immunovirosomes, the retroviral supernatants were mixed with immunoliposomes at equal volumes for 30 min at room temperature before the addition to the cells (1 × 105). In some cases, the retroviral supernatant was treated with DNAse before transduction.
ECs were isolated from human saphenous veins and maintained in culture as described (21,22). Briefly, ECs were cultured in EBM-2 (BioWhittaker, Cambridge, UK) and human endothelial-SFM basal growth medium supplemented with 10% heat-inactivated FCS, 2 mM l-glutamine, 100 U/mL penicillin, 100 μ g/mL streptomycin, 25 μ g/mL fungizone, 0.03 mg/mL endothelial cell growth supplement (ECGS), and 100 U/mL heparin. All cells were used between the 3rd and 4th passages. Human saphenous veins were obtained from patients undergoing varicose vein or coronary artery bypass surgery. Selected patients were either healthy young adults or with coronary artery disease, but without other comorbidity. Patients with diabetes or other autoimmune diseases were excluded from the study. Informed consent was obtained from all patients and approval obtained from the local research ethics committee. To inhibit de novo protein synthesis, the cells were treated with 50 μ g/mL cycloheximide.
Vascular tissues were obtained from the Cardiothoracic Department of Hammer-smith Hospital, UK. The tissues were obtained as a surplus product from coronary bypass surgery, after local research ethics approval, of patients ages 45 to 85 years.
The plasmids—pHIT60 containing gag-pol genes (23), pCL-Eco env containing ecotropic envelope (24), pCOLT-GALV env containing gibbon ape leukemia virus envelope (GALV env) protein (25), or pRV67 env containing vesicular stomatitis virus G envelope (VSV-G env) protein (22,26)—and the retroviral constructs—pBullet-EGFP (22,26,27), LZRS-EGFP (22,26,28,29), pFB-rhGFP (Stratagene, Cambridge, UK) (22,26), or Pinco-EGFP (30)—were used to generate retro-viral particles as described below.
Phoenix ecotropic (30) and amphotropic (23) packaging lines (kind gifts from Dr Gary Nolan’s laboratory, Stanford University) and 293T cells (22,26) were routinely maintained in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% FCS.
The ecotropic MMLV particles were generated as described (26). Briefly, the Phoenix ecotropic cells and 293T cells were cocultured in DMEM at a ratio of 1:1 (1.5 × 106 cells seeded in 25-cm2 flask on the day before transfection). Twenty-four hours later, the retroviral-GFP construct (Pinco-EGFP) together with pHIT60 and pCL-Eco were cotransfected into the seeded packaging cells using a calcium phosphate transfection kit (Invitrogen) according to the manufacturer’s instructions. Sixteen hours after transfection, cells were washed twice with warm PBS and the DMEM was replaced with RPMI-1640. Forty-eight hours after transfection, the viral supernatants were harvested and filtered through a 0.45-μ m pore size filter and stored at –80°C. Retroviral titers of the PINCO vector were determined on NIH 3T3 cells as described (31). The cells were analyzed by flow cytometry to determine the proportion of NIH 3T3 cells expressing EGFP.
The MMLV-based constructs were propagated by a 3-plasmid cotransfection technique in 293T cells as described (22,26). Transfections were performed using polyethylenimine (PEI) (Sigma) on 9-cm tissue culture plates as described (26). In the case, of GALV-pseudotyping, 2 × 106 293T were seeded into a T25 tissue culture flask and 24 hours later transiently transfected with retroviral-EGFP constructs with pCOLT-GALV using a calcium phosphate transfection kit (Invitrogen) according to the manufacturer’s instructions.
MMLV were titred on either D17 cell (VSV-G pseudotyped) or 293 and/or Hela cells (GALV pseudotyped) as previously described (26). In brief cells were seeded on 24 well plates at 3 x 104 cells per well, infected with serial 1:10 dilutions of virus and analyzed for EGFP expression at 3 to 5 days post-infection.
The amphotropic MMLV particles were generated as described (23). Briefly, 2 × 106 amphotropic packaging cells were seeded into a T25 tissue culture flask and 24 hours later transiently transfected with retroviral-EGFP constructs using a calcium phosphate transfection kit (Invitrogen) according to the manufacturer’s instructions. Sixteen hours after transfection, cells were washed twice with warm PBS, and the DMEM was replaced with RPMI-1640. Forty-eight hours after transfection, the viral supernatants were harvested and filtered through a 0.45-μ m pore size filter and stored at –80°C. As described (26), stocks of vectors were titered by infecting 293T and/or HeLa cells with serial 1:10 dilutions of virus and analyzing for EGFP expression at 3 to 5 days postinfection.
For transfection, virosomes and immunovirosomes were generated as described above and cultured with 105 EC cells. The MMLV [with or without polybrene (PB)], virosomes, or immunovirosomes were exposed to cells for 2 h at 37°C. To block targeted endothelial receptors of ECs before transduction, ECs were preincubated with 200 μ g/mL of appropriate antibody at 4°C, then transfected. In some cases, the viral particles were exposed to 50 kGy gamma irradiation.
The phenotype of transfected or untransfected ECs was assessed by flow cytometry 48 h after transfection. Cell staining was performed using mouse antibodies conjugated to APC or primary antibodies followed by goat anti-mouse-APC, as described (19,26). Flow cytometric analysis of all cells was performed using the following mouse monoclonal antibodies: 1.2B6 (anti-CD62E/P) (21), 1.4C3 (anti-CD106) (21), and 6.5B5 (anti-CD54) (21). All antibodies raised from hybridomas were kindly given by Prof. D Haskard, Imperial College London, UK, unless stated otherwise (21).
YOYO-1 stock solution (1 × 10−3 M) (Molecular Probe, Cambridge, UK) was initially diluted 7.5 times in DMSO to a concentration of 1.33 × 10−4 M. The working concentration of YOYO-1 in all samples was 6.3 × 10−6 M. To prevent photo-bleaching of YOYO-1, its solutions were kept in the dark and all experiments were protected from light. The viral particles were labelled with YOYO-1 and visualisation of these labelled particles using flow cytometry was carried out as previously described (33, 35). Uninternalized and surface-bound particles were removed as described (32). Internalization of viral particles was assessed using flow cytometry. In some cases, the cells were treated with chloroquine as described (35).
RT-PCR analysis for EGFP gene expression was carried out as described (36) with the following primers; 5 ′ -GAT CTT GAA GTT CAC CTT GAT GCC (sense) and 5 ′ -AGC TGA CCC TGA AGT TCA TCT GC (antisense) at 60°C annealing temperature. To detect the level of integration of EGFP, we carried out Southern blot hybridization for EGFP DNA in the genomic DNA of transduced cells. Genomic DNA was extracted in accordance with manufacturer’s instructions (Qiagen, Crawley, UK). It was then digested with NcoI (position 4137) and NotI (position 4870) (pBullet-EGFP). Gel electrophoresis and Southern blotting were performed as described (37). The blot was hybridized with [32P]-labeled probe using EGFP fragment released from pBullet-EGFP vector. After 12 h hybridization at 68°C, the blot was washed 3 times in 0.3 × SSC, 0.1% SDS at 68°C before exposing to X-ray film at –80°C for 2 h. The intensity of Southern blot was analyzed as previously described (38).
For multiple comparisons, results were analyzed by ANOVA, whereas for comparison of 2 means, results were analyzed by Student t test where P < 0.05 was considered statistically significant. All data shown are representative of at least three experiments, unless stated otherwise.
As previously reported (19), HSVECs constitutively express CD71 (Figure 1). However, after activation with proinflammatory cytokines (80 ng/mL TNF- α, 80 ng/mL IFN-γ , and 80 ng/mL IL-1β ) for 8 h, the cells upregulate the expression of adhesion molecules (CD62E/P and CD106) and CD71 (21) (Figure 1).
In our experience, MMLV inefficiently transduces HSVECs, in both the presence or absence of polybrene. The addition of liposomes to MMLV has been shown to enhance transduction efficiency (17,18). Using liposomes [Tfx-50 or lipofectin (data not shown) or lipofectAMINE (data not shown)] and amphotropic MMLV [LZRS-EGFP (data not shown), pFB-rhGFP (data not shown), or pBullet-EGFP (Figure 2 with Tfx50 liposomes)], we demonstrated an approximately 10-fold increase in cells expressing EGFP compared with MMLV alone. We investigated whether this could be further increased by incorporation of antibodies. An approximately two-fold increase in expression efficiency was seen with anti-CD71 immunovirosomes compared with virosomes (Figure 2). Similarly, anti-CD62E/P could increase transduction in stimulated HSVECs expressing CD62E/P (Figure 2b). However, as expected from a previous study with immunoliposomes (19), anti-CD106 (Figure 2c) showed only minor or no augmentation. The expression levels of CD106 as determined by flow cytometry were more than CD62E/P on the endothelial cells following 8-h activation (Figure 1) (21). In all cases, the enhanced expression efficiency mediated by an antibody could be blocked with free specific antibody, but not with control antibodies.
Similar augmentation of expression was seen whether the immunovirosomes were made with amphotropic, GALV, ecotropic, or VSV-G coat proteins. In all cases, the presence of liposomes and anti-CD71 antibody enhanced expression efficiency (Table 1). These effects were seen not only on human cells; a specific enhancement of expression efficiency in primary mouse cardiac ECs was also observed using transferrin (in nonactivated ECs) or anti-CD62E (in activated ECs) (data not shown).
We investigated the internalisation of viral particles in target cells by labelling the viruses with fluorescent dye and then following of internalisation of the virus by flow cytometry (using washing with NaOH to remove surface bound material). The data show that when immunovirosomes are targeted at endocytic receptors, such as CD71, there is more rapid uptake than virus alone or incorporated into a virosome (Figure 3a). Chloroquine has been shown to increase gene expression in a number of vector systems, by inhibiting acidification of the endolysosomal pathways and thus increasing the amount of cDNA reaching the nucleus (35). We showed that treatment with this endosomolytic agent can increase cellular entry of MMLV particles in the presence and absence of polybrene. However, less impressive improvement in cellular entry was seen when the particles were packaged by liposomes and immunoliposomes (Figure 3a).
As observed in Figure 2, transduction of HSVECs with MMLV alone and MMLV in the presence of polybrene resulted in poor transduction efficiency. When comparing MMLV transduction of HSVECs in the absence of polybrene with virosomes and immunovirosomes, we saw enhancement in transduction efficiency of ~100-fold and ~250-fold, respectively (Figure 3b). On the other hand, when MMLV transduction in the presence of polybrene was compared to virosomes and immunovirosomes, only ~two-fold and ~five-fold increases, respectively, was observed (Figure 3b).
Cellular treatment with chloroquine can improve transduction efficiency of MMLV alone or MMLV in the presence of polybrene by ~25-fold and ~two-fold, respectively (Figure 3b). However, in the case of virosome and immunovirosome transduction, the addition of chloroquine resulted in only marginal increase in transduction efficiencies (Figure 3b) (albeit statistically significant but probably with limited any biological significance).
The time-course of expression after gene transfer with virus, virosomes, or immunovirosomes was compared. Following amphotropic MMLV, virosome, or immunovirosome transduction/transfection, the early expression of EGFP (less than 24 h) indicated that there was a slow increase in EGFP-positive cells and mean fluorescence intensity of cells (Figure 4) in all methods of transduction/transfection.
After 24 h following amphotropic MMLV gene transfer, the expression of EGFP was stable with only a slight decrease over time in the proportion of cells expressing EGFP (Figure 5). However, in cells treated with either virosomes or immunovirosomes made with anti-CD71 (Figure 5) or anti-CD62E/P (data not shown), there was a decrease over two weeks in the proportion of cells expressing EGFP, at which time expression was equivalent to that seen following retroviral transduction. This reduction in the proportion of EGFP-expressing cells showed a similar kinetics to the reduction in expression seen following transfection with plasmid DNA and liposomes or immunoliposomes alone (with the exception that with these transient nonviral vectors, expression fell to background levels over two weeks) (Figure 5a, lower panel).
We compared the kinetics of mRNA expression following treatment with amphotropic MMLV (Figure 6, pBullet-EGFP) (LZRS-EGFP, data not shown), virosomes, or immunovirosomes. As can be seen in Figure 6, upper panels, expression of EGFP mRNA was similar at all times following retroviral gene transfer. However, following treatment with either virosomes or immunovirosomes, EGFP mRNA expression was higher at early time-points but decreased over time to reach levels comparable to retroviral-transduced levels [shown for anti-CD71 monoclonal antibodies for activated EC (Figure 6, upper panels), but similar data (not shown) were seen with anti-CD71 for nonactivated EC and anti-CD62E/P for activated EC].
To assess the persistence of EGFP gene integrated into the EC genome, we carried out Southern blot analysis of genomic DNA derived from ECs following gene transfer. Interestingly, the data showed that the number of copies of EGFP integrated into EC genomic DNA remained stable at all times following treatment with viruses, virosomes, or immunovirosomes (Figure 6, lower panels).
To exclude the possibility that the augmentative effects of liposomes and immunoliposomes were due merely to the transfer of fluorescent protein (produced in the packaging cell) by the viral particles, the particles were irradiated (90 kGy) before use. As can be seen (Figure 7a), no expression of EGFP seen after irradiation, indicating that passive uptake of fluorescent viral particles was not responsible. This was further confirmed by treating HSVECs with cycloheximide. Again, no EGFP expression was seen, indicating that EGFP expression is due to the de novo synthesis rather than transfer of EGFP protein (Figure 7b).
To exclude the likelihood that the EGFP-containing plasmids used to make the retrovirus particles, which might still be present in the viral supernatants, were responsible, we treated the supernatant with DNAse before use. As can be seen Figure 7c, treatment of DNAse had minimal effect on gene expression, indicating that carryover of EGFP plasmids were unlikely to be the cause.
We have demonstrated a quick and easy method to alter viral tropism without the need of generating genetic modification of viral capsid proteins. This allows a rapid assessment of the consequences of changing viral tropism in terms of transfection efficiency and cell-type specificity. In addition, we also highlighted that altering viral tropism to allow viral entry through highly endocytic receptors can increase transfection efficiency transiently but has no effect on proviral integration.
Since the initial description of lipofection as a mean of DNA transfection (39), cationic liposomes have been widely used for gene delivery both in vitro and in vivo (40,41). We, like others, have used liposomes to package viral particles to increase the infectivity (17,18,42). Using immunoliposomes targeted to endothelial receptors, such as CD71 (nonactivated ECs) or activated endothelial receptors, such as CD62E/P, we can enhance gene transfer of MMLV. We showed selectivity of viral tropism when viral particles were complexed with immunoliposomes containing anti-CD71 antibodies. Although expression of CD71 is high on ECs, its ubiquitous expression restricts its use as a specific target for gene delivery. We have, therefore, developed this approach with anti-CD62E/P. This allows a target-specific delivery of viral particles to activated ECs. On the other hand, other adhesion molecules, such as CD54 (data not shown) and CD106 expressed by activated ECs (21), did not show enhancement of transduction efficiency. Our observations suggest that the cellular receptors chosen to be targeted are important in determining the success of the receptor-mediated approach. Whereas some antigens may be attractive targets in terms of patterns of expression, they are poor at delivering the viral particles to the appropriate cellular compartment. For example, even though CD106 has been shown to internalize through clathrin-coated vesicles (43), when the molecule is bound by antibody, it is shed rather than internalized (44). CD54, on the other hand, has a 10-fold lower endocytosis rate than E-selectin (19,45).
As MMLV on its own has poor transduction efficiency on HSVECs, we have therefore chosen this group of viruses as a model. On the basis of their host range, MMLVs have been classified into six subgroups (ecotropic, amphotropic, polytropic, xenotropic, MDEV, and 10A1) (9). The envelope motifs that bind to the various viral receptors and determine the infection specificity have been mapped within the N-terminal one-third of the surface protein SU (gp70), which bears the most variable regions of MMLV envelope (46–48). Thus, ecotropic MMLV enters cells after binding to a cationic amino acid transporter (CAT-1 or REC1) (49), and amphotropic MMLV enters cells after binding to a sodium phosphate symporter (PIT-2 or GLVR1) (50,51). However, the fine mechanism by which retro-viruses enter the cell is one of the most poorly understood aspects of the viral life cycle. We have shown that MMLV pseudotyped with various viral envelopes [amphotropic, ecotropic, gibbon ape leukemia virus (GALV), vesicular stomatitis virus G (VSV-G) (Table 1)] can be targeted using immunoliposomes, indicating that the coat protein has little effect on the interaction of the virus with liposomes or their subsequent delivery to cells. By generating immunovirosomes, there are three independent pathways for cell entry which likely will compete with each other. Our data suggest the most efficient pathway of entry would be the predominant entry delivery mechanism in our mixed system. It is therefore not surprising that viral entry pathway mediated by its pseudotyped envelope is negligible, as it represents the slowest entry pathway (Figure 3).
Using virosomes or immunovirosomes targeting at highly endocytic receptors, we could improve transduction efficiency of MMLV alone by ~100- and ~250-fold, respectively. Compared with MMLV transduction in the presence of polybrene, however, these increases are less impressive. These findings are not surprising, as the use of polybrene is a well-optimized method to improve transduction efficiency of MMLV in vitro. Whereas the use of polybrene to assist transduction of MMLV is effective in vitro, its application for in vivo transduction is limited. On the other hand, virosomes or, in our case, immunovirosomes may allow in vivo application (18).
Parameters that control the kinetics of transduction of viral vectors are poorly understood. The first step is binding of the virus to its receptor on the cell surface. This is thought to be the rate-limiting step of the infection process (52). It has been argued that the Brownian motion of viral particles in the medium imposes a significant limitation for infection of adherent cells (53). However, the binding kinetics of MMLV vectors to cells in suspension fits a bimolecular, noncooperative model, which rapidly reaches equilibrium at 37°C when virus is in excess (54). The association rate constant is significantly lower than the calculated limitation imposed by viral diffusion, suggesting that binding, rather than encounter, is the rate-limiting step (55). In our experiments, the cells were exposed to viral particles with or without liposomes or immunoliposomes for 2 h. Longer time exposure to viral particles often results in higher cellular toxicity (data not shown). The use of immunoliposomes or liposomes may increase the rate of binding of MMLV.
Further studies have shown that MMLV infection follows internalization of intact virions by endocytosis, followed by a membrane fusion event releasing virion cores to the cytoplasm (56,57). To determine if MMLV transduction is endocytosis dependent, we showed that transduction efficiency could be augmented by treating the cells with the endosomolytic agent chloroquine, as previously reported (58). This suggests that once the complex is internalized, it is directed into the endolysosomal pathway. By inhibiting the lysosomal enzymes with the endosomolytic agents and thereby increasing endolysosomal escape, gene expression was increased. However, in the case of virosomes and immunovirosomes, treatment with the endosomolytic agents resulted in only a marginal improvement in the number of viral particles retained intracellularly and productive transduction. This may be because the efficient delivery of viral particles overwhelms the degradation capacity of endolysosomal pathways. However, with a less efficient delivery system such as MMLV alone or in the presence of polybrene, these pathways have more influence on the total number of particles remained intracellularly (Figure 3a) at the 4-h time-point and the productive transduction (Figure 3b).
The enhancement of expression with immunovirosomes or virosomes was transient. Previous groups have also shown short-term expression after transduction with either lentivirus or MMLV. This could be due to transfer of protein by the viral particles (59,60) or, in the case of viruses that have been disabled in such as a way as to prevent either reverse transcription of RNA or integration of virally derived DNA into the host genome, as a result of direct translation from virally delivered RNA (61) or transcription of episomal viral DNA (60,62). Such “pseudo-transduction” has been suggested both as a way of transient expression of toxic proteins (61) and as a safe, nonintegrating, viral vector for gene therapy (62).
The reason viral particles, when delivered into a cell using immunovirosomes or virosomes, are unable to enhance the integration of the virally derived DNA into the genome is not clear. We have previously reported that HSVECs are actively dividing cells (21), and stable integration was seen with MMLV alone, indicating that lack of enhancement in integration with virosomes or immunovirosomes is not due to cell division or cell senescence. It is interesting to speculate that the mechanism of transduction occurring with virus alone versus virosomes or immunovirosomes might be different. Our data suggest that pseudo-transduction due to delivery of fluorescent proteins is unlikely to be the cause for lack of integration seen with virosomes or immunovirosomes. Early EGFP expression data indicate that de novo synthesis of EGFP protein is required. Owing to increased delivery of retroviral RNA with virosomes and immunovirosomes, direct translation from virally delivered RNA (60) or transcription of episomal viral DNA (59,61) may be possible. It may also be possible that sites for retroviral integration in the human genome are a rate-limiting step for viral transduction. We cannot exclude that the use of liposomes may interfere with the integration process.
Modifications of the structure of the virus capsid proteins and expression cassette to generate vectors that are highly selective and efficient for target cell binding and entry have been described (6). For example, fusing a gene for a single chain antibody (sFv) to the region of the envelope gene encoding its N-terminal amino acids has been carried out (63). This technique has been attempted using different sFvs and other proteins capable of specifically attaching to cellular receptors (62). Most have resulted in very low infectivity, less than 3%, and poor virion stability (63). It is therefore difficult to compare the approach with our approach.
It may be possible to exploit the different pathways utilized by virus alone or virosomes/immunovirosomes to alter the behavior of retroviral vectors. Retroviral vectors are likely to be of greatest use in the context of requiring long-term expression of transgene. However, nonviral vectors or adenovirus that resulted in transient expression of transgene may be useful for clinical settings requiring transient expression. In our system, we saw biphasic expression profile with higher and transient expression followed by low and sustained expression of transgene. This might be in particular useful for transplantation, as the initial expression of an immunomodulatory transgene would be required at higher levels to prevent acute rejection (3). Later and sustained expression of this transgene might be required to prevent chronic rejection or maintain tolerance (3).
The successful utilization of a new generation of viral vectors in the clinic may well pave the way for superior gene delivery systems in the future that specifically deliver the therapeutic gene to a particular target cell. Immunovirosomes may offer an opportunity to address some of the current deficiency of viral vectors, in particular for transplantation (3), and to test different targets for gene transfer. They can be easily and quickly assembled, avoiding complicated molecular engineering of the viral envelope. However, it is important to understand how these vectors alter long-term expression of genes in target cells. Our findings have significant implication for viral vector design and improved tropism.
This research is supported by a Research Training Fellowship from the MRC and the Royal College of Surgeons Edinburgh 2001–2004 (PHT) and project and program grants from the BBSRC and the MRC (AJTG). AJTG was a BBSRC Research Development Fellow. The authors thank Prof. K Taylor and his team for supplying human vascular tissues for the work and the theatre nursing staff at Hammersmith and St. Mary’s Hospitals for collecting and preserving human vessels.
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