Human gene therapy: A cure for all ills?

Human gene therapy: A cure for all ills?

Public opposition to genetically modified (GM) crops in the UK and Europe has propelled the issue to the top of the political agenda. At the same time, there is growing public interest in the potential costs and benefits of applying the techniques of genetic modification to treating human illness and disease. This briefing examines the case for gene therapy and considers the safety, social and ethical concerns.

What is gene therapy?

GENE therapy is defined as ‘the treatment or prevention of disease by gene transfer'[1] and involves the genetic modification of human cells by introducing one or more new genes. There are two types of gene therapy – somatic and germ line:

* Somatic cell gene therapy involves the genetic modification of any cells in a patient’s body apart from the reproductive cells (egg and sperm). The intention is to confine changes to the individual being treated and the parts of the body where the illness is experienced (such as the lungs with cystic fibrosis) so the genetic alteration should not be passed on to the patient’s children. Somatic cell gene therapy is the only form that is permitted in the UK.

* Germ line gene therapy involves genetically modifying a fertilised egg and therefore will affect not only the individual that develops from it, but also their offspring and successive generations. Because no actual therapy of an individual is involved, it is more accurately called germ line gene transfer. Although germ line genetic modification of plants and animals is now commonplace, germ line genetic modification of humans is currently banned in the UK. This is in line with an existing world-wide consensus that such techniques should not be allowed because of the serious ethical and health implications of modifying the human germ line.

A variation of somatic cell gene therapy is ‘in utero’, where a foetus is modified within the womb or, in the case of embryos, in a test tube (in vitro). However, gene therapy on the somatic cells of a foetus or embryo carries a significant danger of inadvertently affecting the reproductive cells of the baby and hence becoming germ line gene therapy ‘by default’. For this reason, in utero gene transfer is not allowed in the UK.

Different approaches to gene therapy

There are five ways in which gene therapy has so far been approached:
* Gene augmentation or addition – in situations where a gene is faulty, a normal working version can be introduced to take over its functions.
* Gene inhibition – in situations where a faulty gene is producing a harmful product, it can be switched off by an introduced gene.
* Targeted gene mutation – a faulty gene is repaired by using genetic techniques to correct the defect.
* Killing of disease cells – genes which cause the production of a toxin can be targeted into diseased cells such as cancer cells or cells infected with a virus. Once inside the cell, the toxin produced by the gene kills the diseased cell.
* Targeting the immune system to kill disease cells – a gene which causes the production of a protein recognised as foreign by the patient’s immune system is targeted into diseased cells such as cancer cells. The patient’s immune system then attacks and kills the cells.

Only the first three approaches are aimed at correcting genetic (inherited) disorders. The last two are part of targeting systems to treat, not prevent or correct, a disease and are sometimes referred to as ‘gene-based’ immunotherapy or cancer therapy.

Gene therapy trials

Attempts are currently being made to apply gene therapy research to a whole range of diseases, including inherited disorders such as muscular dystrophy and cystic fibrosis as well as cancers and heart diseases. In North America and Europe, approximately two-thirds of clinical trials of gene therapy in humans have been cancer treatments. The majority of the rest have focused on inherited ‘single gene’ diseases (i.e. where one faulty gene is responsible), particularly cystic fibrosis, which is one of the most common inherited diseases (see Table 1). Studies have also been conducted using gene therapy to treat infectious diseases (such as HIV), cardiovascular diseases and rheumatoid arthritis[1]. In the UK, of 41 gene therapy trials approved between 1993 and 2000, 30 have been for different forms of cancer, 8 for single gene disorders and 1 for HIV3. However, there have been no applications for trials on single gene disorders since 1996.

Most research work is being undertaken with experimental animals. For example, a gene to increase red blood cell production (the EPO gene) has been introduced into mice and monkeys[4,5]. Another gene (the IGF-1 gene) has been introduced into mice to increase muscle mass. Although these approaches could be used for the treatment of diseases, they could, for instance, also be used to enhance performance in athletes and will be virtually impossible to detect 6. Such research demonstrates that as well as work on genetic disorders and cancer treatments, developments in gene therapy could also be open to abuse.

How successful has gene therapy been to date?

Gene therapy is proving to be considerably more technically challenging than was originally predicted and progress has been very slow[1]. Since the first human trials in 1990, there have been over 400 research studies world-wide[7]. However, only one clear ‘life-saving’ success has so far been recorded, with researchers in France treating two babies over a 10-month period with severe combined immuno deficiency (SCID), a single gene disorder that causes the immune system to fail[8].

Gene therapies for cancer, limb ischaemia (lack of blood supply) and HIV have progressed to trials in affected patients. Although some clinical benefit has been recorded, no dramatic improvements have been achieved except, recently, in the case of limb ischaemia[9]. Here, genetic material was injected into the muscles of affected limbs and stimulated blood vessel growth quickly enough to restore blood supply where, in some cases, patients would otherwise have faced amputation. Some success in reducing the size of head and neck tumours has also been reported recently[10]. This was in cases where the tumours were very advanced at the time of treatment, raising the hope that earlier treatment may be more successful.

However, most gene therapy studies are still in their early stages, aimed only at investigating whether genes are successfully being transferred and whether the process of transfer is safe. Lack of any significant progress to date means gene therapy is still officially defined in the UK as ‘research’ rather than ‘innovative treatment’.

Technical difficulties with gene therapy

Gene therapy raises the prospect of treatments for diseases which, until now, there has been no real hope of treating. However, inflated claims about the potential for gene therapy continue to raise expectations which, in the medium term at least, are unrealistic. For gene therapy to work, the correct genes have to enter the correct cells and operate for a prolonged period (the lifetime of the patient in many cases) without ill effects. Serious problems remain at each stage in achieving this:

1. Identifying the genetic fault
Working out whether there is a genetic component to an illness and what this consists of is fraught with problems. Only a small number of diseases (approximately 2% of all illnesses) – such as cystic fibrosis or Huntingdon’s disease – are directly linked to the presence of a single faulty gene (a single gene disorder). However, even in single gene disorders there can be considerable variation between patients in severity or time of onset of the disease. In the case of Alzheimer’s disease, for example, age of onset often differs by many years, even in identical twins[11].

A much larger number of diseases can be directly linked to the negative impact of environmental abuses such as malnutrition, chemical pollution or smoking, and, in practice, the majority of diseases, including cancers and heart diseases, are produced through a complex interaction between environmental and genetic factors. (In the case of breast cancer, for example, only 5-10% of all cases are thought to be related to the presence of a defective gene and having one of these ‘breast cancer genes’ does not, in itself, guarantee that a woman will develop the disease[12].)
Therefore, an important challenge for scientists is to understand how gene-environment interaction works.

2. Delivering the new genetic material into the patient’s cells and keeping it working
Gene therapy research continues to be hampered by the difficulty of inserting genes into cells[7]. Cells can be modified while they are still in the patient (in vivo) or removed – as in the successful SCID trial – treating them in a test tube and then returning them to the patient (ex vivo). Ex vivo gene therapy is more efficient in terms of gene transfer but it is patient-specific and more costly than in vivo. In vivo approaches, as are being attempted with cystic fibrosis, have problems modifying enough cells to have an effect.

At present, viruses (including adenoviruses, adeno-associated viruses, retroviruses and lentiviruses) are the most common means or ‘vectors’ used to introduce the new genetic material into cells because viruses are naturally well equipped to infiltrate cells. Other ways of delivering genetic material using either non-viral vectors (such as packaging genes into fatty droplets called liposomes which are taken up by cells) or physical methods (such as directly injecting genes – so-called ‘naked’ DNA) are also being developed. All have pros and cons. Viruses may trigger an immune reaction rendering the newly inserted genetic material ineffective and some (e.g., retroviruses) are relatively poor at invading non-dividing cells. Physical methods tend to be short-lived, with gene expression only lasting a matter of days or weeks. The search for a reliable vector remains one of the biggest challenges for gene therapy.

3. Side-effects
In theory, the viral vectors used in gene therapy are ‘disabled’ so they should not be able to replicate and spread. However, there is a risk that this safeguard could break down and endanger the patients and others. Even if harmless, an immune response may be triggered to ‘fight off’ a virus vector. In September 1999, 18-year-old Jessie Gelsinger, who suffered from a rare genetic liver ailment (although his life was not threatened by it), died while taking part in a gene therapy trial at the University of Pennsylvania. The trial used an adenovirus vector[13] and it seems Gelsinger died from a massive immune response to the vector[14]. In animal experiments, lentiviruses (a group of viruses including HIV) also appear to have caused liver damage[15].

As it is not possible to control where the new genes are inserted, they could be introduced into the patient’s genes and result in mutations which could cause illness in the future. This potential problem is greatest for those virus vectors (retroviruses, adeno-associated viruses and lentiviruses) which result in the new gene being integrated in the patient’s DNA. There is also thought to be a remote but real chance that if a retrovirus was wrongly inserted, it might promote cancer[14]. In animal experiments, genetic modification has resulted in disruptions in adjacent genes[16].

This scenario may be more likely with in utero gene therapy where, as a professor of Cell Biology and Anatomy at New York Medical College has pointed out, ‘The biology of the developing individual will … be profoundly altered by the manipulation on his/her genes at an early stage. Laboratory experience shows that miscalculations in where genes are incorporated into the chromosomes can lead to extensive perturbation of development. The disruption of a normal gene by insertion of foreign DNA in a mouse caused lack of eye development, lack of development of the semicircular canals of the inner ear, and anomalies of the olfactory epithelium, the tissue that mediates the sense of smell.'[17]

4. The push towards germ line gene transfer
One of the outcomes of these technical difficulties in getting gene therapy to work has been the emergence of pressure in the scientific community to allow germ line gene transfer because they consider it may be technically easier to do. For example, by altering genes in the fertilised egg, the genes should be included in all cells as the embryo divides and forms a baby, removing the problem of only a limited number of cells being altered as is the case with somatic cell therapy. Other developments in genetic technologies, such as embryonic stem cell cloning, also make germ line gene transfer more feasible. Under the guise of opening a debate on the subject, the US gene therapy entrepreneur W. French Anderson submitted a draft proposal to the US National Institutes of Health (NIH) to begin germ line gene transfer experiments on human foetuses[18].

However, germ line gene therapy brings risks to the individual involved as interfering with genes in this way could have very damaging consequences if other genes are disrupted. Furthermore, because the changes will also be passed on to any offspring, the human gene pool will be altered irrevocably. It also raises the disturbing prospect of ‘designer babies’ and even eugenics (‘the study and practice of methods designed to improve the quality of the race, especially by selective breeding'[19]).

The problem of genetic determinism

The genome of an organism is all the genetic (hereditary) information it contains. In June 2000, it was announced that a draft ‘map’ of 95% of the human genome had been completed. The news was hailed by politicians, scientists and media columnists alike as a historic breakthrough, with then US President Clinton calling the announcement ‘more than just a triumph of science and reason. Today we are learning the language in which God created life'[20]. It is now commonplace to see the genome described in quasi-religious terms such as ‘the book of life’ and it would appear that genes are being given a God-like status in determining our future[21].

To place genes on a pedestal in this way takes attention away from the complex interaction between biological (internal) and environmental, social and cultural (external) factors responsible for most diseases. This is unhelpful and dangerous in relation to gene therapy for several reasons:

* It raises highly unrealistic expectations concerning the potential of gene therapy. This is likely to lead to considerable disappointment for individual patients. 

* Political attention (and therefore funding) is likely to shift further and further from tackling social problems such as poverty and environmental pollution which are more important in illness prevention.

* The false belief is likely to be increasingly promoted (even among scientists) that a whole range of aspects of human psychological health, performance and behaviour can be reduced to a one-to-one correspondence with particular genes or groups and families of genes. For example, researchers at the Salk Institute in La Jolla, California, claim to have found a ‘neurosis’ gene even though ‘neurosis’ is a label for a complex cluster of human behaviours, not a single disease[22].

The commercialisation of gene therapy research and its implications

It is clearly in the interests of the genomics industry to argue that genes are the most important cause of disease, given the commercial pressure to develop and retain investor confidence in a promise of drugs and treatments for the future. The multinational pharmaceutical companies Aventis and Novartis in particular have made large investments in this research field.

Public and private research are also becoming inextricably intertwined and ‘company sponsorship is pervasive in gene therapy'[14]. For example, SmithKline Beecham has been working with the University of Cambridge and the Medical Research Council’s Dunn Nutrition Unit on the control of energy metabolism and the identification of a ‘lean gene’ in a search for treatments for obesity[23]. Oxford BioMedica, a UK gene therapy company, was set up by two Oxford University professors ‘armed with six patents from their work in the university lab'[24].

Mixing private and public funding raises questions about the control of the trajectory of research and conflicts of interest may arise in gene therapy trials. In the Gelsinger case, the technique used was patented by the institute’s head, James Wilson, and both he and Pennsylvania University have a financial stake in a company developing the technology.[14]

Against a backdrop of genetic ‘hype’, secrecy, the privatisation of basic knowledge and profit-driven motives, the benefits of gene therapy may not only be more elusive than predicted, they may also be restricted to the few who can afford them. In the meantime, corners are likely to be cut in safety testing. Evidence of such trends is already emerging.

Secrecy in safety testing

Gene therapy is big business but, as with the so-called ‘’ companies, genomics companies are trading on a promise of what might be in the future. They rely heavily on gaining investor confidence in this promise, so news of deaths in gene therapy trials is extremely damaging. Since the death of Jessie Gelsinger in a gene therapy research trial, there have been a number of accusations of cover-ups of adverse effects in the USA[25].

For example, the US Food and Drug Administration (FDA) sent a warning letter to a cardiac specialist at St. Elizabeth’s Medical Center in Boston saying that ‘a death was not properly reported'[14]. In another case, Ronald Crystal of the New York Hospital reported a gene therapy death to the US authority but requested that the letter be ‘kept confidential and not part of the public record'[25]. At the time, Crystal’s biotechnology company, GenVec, had filed to make an initial public stock offering although he said this had not influenced his request for confidentiality. The company subsequently decided not to go public.

It has proved difficult to gather detailed information on gene therapy trial success rates and adverse reactions in the UK. The Gene Therapy Advisort Committee’s (GTAC) Adenovirus Working Party reported in June 2000 that there had been 69 patients involved in 11 adenoviral gene therapy research trials and that ‘no major or life-threatening toxicity had occurred'[26].

Genetic modification for profit rather than gene therapy for health

The way in which profitability influences attitudes to gene therapy was graphically demonstrated in an article in a scientific journal commenting on the success with the SCID gene therapy trial[27]. The news was considered of ‘commercial insignificance’, because ‘the new data are barely relevant to gene therapy companies, most of which are hoping to treat the large patient populations suffering from cancer, HIV, and other complex diseases. Indeed, stocks of such companies as Introgen Therapeutics (Austin, TX) and Targeted Genetics (Seattle, WA) were not affected by the news’.

This focus on profitability has serious consequences. The number of people affected with serious single gene disorders (or so-called ‘minority diseases’) is relatively small, making research in this area commercially unattractive even though, on current evidence, this group could be the easiest to treat with gene therapy. The profit motive also means that the interests of the rich may drive the exploitation of the technology. There are already fears that gene therapy may be misused in sport[6]. Desirable ‘improvements’ to people’s appearance, skills and personality could become the target of gene therapists and herald the prospect of designer babies.

A new social divide between the genetically advantaged and disadvantaged could arise. The creation of two distinct species built upon such a distinction is nearing reality rather than being science fiction. Chromos Molecular Systems Inc. in British Columbia is currently developing artificial human chromosomes[28]. People who were given artificial chromosomes and who wanted to pass complete sets of these to their children intact would only be able to mate with others carrying the same artificial chromosomes. This condition, called ‘reproductive isolation’, is the primary criterion that biologists use to classify a population as a separate species.


Gene therapy not only brings the prospect of treatments for previously untreatable illnesses, it may also enable the prevention of certain diseases through the correction of genetic disorders. However, it is clear from gene therapy under development that, in the short to medium term, most gene therapy will not be used for prevention but for developing more effective ‘gene-based’ treatments for cancer and AIDS.

Although gene therapy has been heralded as a major breakthrough in medical science, it also carries the potential for abuse and for commercial imperatives, not human need, to drive its progress. The demands of industry in maintaining investor confidence may increase the dangers to patients through secrecy and poor supervision. Placing too much emphasis on genes as the determining factor in health and disease may lead to prolongation of suffering as a result of other underlying causes being neglected. It may also give rise to new insidious practices of genetic discrimination in areas such as employment, insurance and health care. Avoiding the pitfalls whilst reaping the benefits of gene therapy is the challenge for politicians and regulators. Crucially, society must not be overcome by ‘genetic determinism’ or ‘genetic thinking’ and the hype of the biotechnology companies if health care issues are to be addressed effectively.


1 Mountain, A. (2000) ‘Gene Therapy: the First Decade. Tibtech 18: 119-128.
2 Gene Therapy Advisory Committee Report on the Potential Use of Gene Therapy in utero, November 1998. GTAC: London.
3 Data supplied by Gene Therapy Advisory Committee Secretariat, August 2000.
4 Svensson, E.C. et al (1997) ‘Long-term erythropoietin expression in rodents and non-human primates following intramuscular injection of a replication-defective adenoviral vector.’ Human Gene Therapy 8: 1797-1806.
5 Zhou, S. et al (1998) ‘Adeno-associated virus-mediated delivery of erythropoietin leads to sustained elevation of hematocrit in non-human primates.’ GeneTherapy 5: 665.
6 Aschwanden, C. (2000) ‘Gene Cheats’. New Scientist, 15th January pp 24-29.
7 Zanjani, E.D. and Anderson, W.F. (1999) ‘Prospects for in utero Human Gene Therapy’. Science 285: 2084-2088.
8 Cavazzana-Calvo, M. et al (2000) ‘Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease’. Science 288: 669-672.
9 Baumgartner, I. et al (1998) ‘Constitutive expression of phVEGF165 following intramuscular gene transfer promotes collateral vessel development in patients with critical limb ischemia.’ Circulation 97: 1114-1123.
10 ‘Gene therapy shrinks tumours’. The Times, 1 August 2000.
11 Finch, C.E. and Tanzi, R.E. (1997) ‘Genetics of Ageing’. Science 278: 407-411.
12 Yang, X. and Lippman, M.E. (1999) ‘BRCA1 and BRCA2 in breast cancer.’ Breast Cancer Research and Treatment 54(1): 1-10.
13 Lehrman, S. (1999) ‘Virus treatment questioned after gene therapy death’. Nature 401: 517-518.
14 Marshall, E. (2000) ‘Gene therapy on trial’. Science 288: 951-956.
15 Park, F. et al (2000) ‘Efficient lentiviral transduction of liver requires cell cycling in vivo’. Nature Genetics 24 (1)19-52.
16 Woychick, R.P. et al (1985) ‘An inherited limb deformity created by insertional mutagenesis in a transgenic mouse’. Nature 318: 36-40.
17 Newman, S.A. (2000) ‘The hazards of human developmental gene modification’. GeneWatch 13(3): 10. Council for Responsible Genetics: Cambridge, MA.
18 ‘Risks inherent in fetal gene therapy’. Nature 397: 383, 4 February 1999.
19 British Medical Association (1998) Human Genetics: Choice and Responsibility. Oxford University Press.
20 ‘World Leaders Hail Historic Breakthrough as Scientists Map the Human Genetic Code’. The Scotsman, 27 June 2000.
21 Nelkin, D. (2000) ‘Less Selfish than Sacred? Genes and the Religious Impulse in Evolutionary Psychology, in Alas, Poor Darwin. H Rose & S Rose (eds). Jonathon Cape: London.
22 ‘Now the worrying news – neurosis gene is discovered’. The Independent, 3 April 2000.
23 Clapham, J.C. et al (2000) ‘Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean’. Nature 406: 415-418.
24 ‘Inside the dream factory’. The Independent, 16 August 2000.
25 Wadman, M. (1999) ‘NIH panel to limit secrecy on gene therapy’. Nature 402: 6.
26 Report of the GTAC Adenoviral Working Party, June 2000. GTAC: London.
27 ‘Small success for gene therapy’. Nature Biotechnology 18 (6): 592-593. June 2000.
28 ‘Pass it on’. New Scientist, 8 July 2000 p. 7.

The above was first published as a GeneWatch UK briefing paper (No.12, October 2000). GeneWatch UK is an independent, voluntary, not-for-profit organisation working to promote environmental, ethical, social, human health and animal welfare considerations in decision-making about genetic engineering and other genetic technologies.


The regulation of gene therapy in the UK

IN the UK, permission to conduct gene therapy research has to be obtained from a Department of Health advisory body known as the Gene Therapy Advisory Committee (GTAC) in conjunction with the appropriate Local Research Ethics Committee and the Medicines Control Agency (MCA). Researchers are required to notify any adverse effects from their trials to all three of these bodies. GTAC operates six key principles when licensing gene therapy trials:
1. Gene therapy is research and not an innovative treatment because it has not yet been sufficiently developed.
2. Only somatic cell therapy should be considered.
3. In view of safety and ethical difficulties, germ line interventions are not allowed.
4. Gene therapy should be restricted to life-threatening disorders where no alternative effective treatments are available.
5. Patients should take part in gene therapy research trials only after a full explanation of the procedures, risks and benefits and after they have given their informed consent.
6. For those not able to give consent, including young children, the research must not put them at disproportionate risk.

GTAC also considers that in utero gene therapy is not permissible[2].


Gene therapy with your salads, anyone?

A virus is simultaneously being genetically modified to kill insect pests and to transfer genes into human cells in gene therapy. Prof. Joe Cummins points to a major gap in biosafety regulation.

DO our biosafety regulators know that a certain virus is being genetically modified to control plant disease and to serve as a gene carrier or vector for human gene therapy? This is the baculovirus, a virus previously thought to infect only insects but which has since found to get into all kinds of mammalian cells, including those of human beings. Farm workers spraying crops with anti-insect baculovirus and the public eating the crop not properly washed may both become genetically modified as a result.

Pests that infect and cause disease symptoms in both crops and human cells have never been described. Yet natural viruses that infect and slowly kill insects are also known to infect humans, but the infected humans do not seem to have symptoms. However, when the virus is genetically modified to eradicate insect pests, it may cause disease symptoms in those spraying crops or eating the sprayed crop. The baculovirus manipulated for insect control and for human gene therapy has been proven to be genetically unstable, and is prone to recombination and deletion at high frequency [1]. Such genetic instability, which has been noted repeatedly by those studying the virus, makes toying with it like playing with explosives.

Natural baculovirus, in contrast, is very stable and may remain dormant in the environment for years before infecting insects. The virus alone has a relatively low killing power and slow action. When a gene for a potent toxin such as scorpion toxin or a gene affecting a juvenile hormone is added to the virus, it kills faster and fewer insects survive infection. Numerous field tests of modified virus sprayed on crops have been done, despite protests from the public.

Soon after GM virus were developed for insect control, it was found that baculovirus is capable of infecting human liver cells and produced relatively little toxicity to the infected cells. For that reason, baculovirus vectors were developed to treat liver disease. Soon, baculovirus vectors were even developed to transfer genes to the human brain [2]. The fact that baculovirus can infect human liver or brain cells seems to have been ignored by those developing the virus for commercial pest control. There has been a great deal of pressure to hasten approval of the GM baculovirus for pest control especially in the United States and Canada, where human populations have already been used as guinea pigs for GM crops.

Ecological impacts of recombinant baculovirus insecticides have focussed on baculovirus containing scorpion toxin because that construction has been most widely used [3]. Impacts on non-target insects are simply extrapolated from findings on insects of related phylogeny, a practice that is full of pitfalls, for simply adding and deleting genes can change the host range of the resultant baculovirus in unpredictable ways [4]. Furthermore, the recombinant baculoviruses were very persistent, and capable of
reshaping an ecosystem.

The scorpion toxins used with recombinant baculovirus have been selected to avoid toxicity to humans and, as much as possible, to non-target animals. However, the allergenicity and other harmful effects in human liver infection have not yet been investigated.

Recombinant baculoviruses have also been constructed containing other genes, such as those coding for Bacillus thuringiensis (bt) toxins [5], which are known to produce allergic reactions in human beings and are also harmful to rats [6]. A recombinant baculovirus has even been constructed containing an antisense fragment to the c-myc oncogene [7]. The c-myc oncogene is a modified form of an essential cellular gene. Thus, the antisense gene, which contains a DNA sequence complementary to the gene itself, may end up inactivating an essential cellular function.

Baculovirus vectors efficiently transfer genes into human liver cells [8, 9]. Hybrid baculovirus-adenovirus vectors have also been used to deliver genes to human cells [10].

In conclusion, baculovirus vectors are being used to control insect pests because they are effective and persist for a long time in the environment. Baculovirus vectors are also being used in gene therapy of the human liver and brain. These areas of research seem to exist as two solitudes and the risks of one are not evaluated in the context of the other. We may be treated to liver and brain gene therapy with our salad whether we need it or not.

1. Wu,Y, Lui,G and Carstens,E ‘Replication, integration, and packaging of plasmid DNA cotransformation with baculovirus viral DNA’ 1999 J Virol 73,5473-80.
2. Sarkis, C, Serguera, C, Petres, S, Buchet, D, Ridet, J L, Edelman, L and Mallet, J, ‘Efficient transduction of neural cells in vitro and in vivo by a baculovirus-derived vector’ 2000 ProcNatnlAcadS ci97: 14638-14643.
3. Richards,A,Matthews, M and Christain, P ‘Ecological considerations for the environmental impact evaluation of recombinant baculovirus insecticides’ 1998 Ann Rev. Entomol 43,493-517.
4. Thiem,S ‘Prospects for altering host range for baculovirus bioinsecticides’ 1997 Curr Opin Biotechnol 8,317-22.
5. Martens, J, Knoester, M, Weijts, F, Groffen, S, Hu, Z, Bosch, D and Vlack, J, ‘Characterization of baculovirus insecticides expressing tailored Bacillus thuringiensis Cry1A9b) crystal proteins’ 1995 J Invertebr Pathol 66,249-57.
6. Fares, N H and El-Sayed A K, ‘Fine structural changes in the ileum of mice fed on endotoxin-treated potatotes and transgenic potatoes’. Natural Toxins:1998: 6: 219-33.
7. Lee, S, Qu, X, Chen, W, Poloumieko, A, MacAfee, N, Morin, B, Lucarotti, C and Krause, M ‘Insecticidal activity of a recombinant baculovirus containing an antisense c-myc fragment’ 1997 J Gen Virol 78,273-81.
8. Hofmann, C, Sandig, V, Jennings, G, Rudolph, Schlag, P and Strauss, M ‘Efficient gene transfer into human hepatocytes by baculovirus vectors’ 1995 Proc. Nantl Acad Sci USA 92,10099-103.
9. Boyce, F and Bucher, N ‘Baculovirus-mediated gene transfer into mammalian cells’ 1996 Proc. Natnl Acad Sci USA 93,2348-52.
10. Palombro, F, Mociotti, A, Recchia, A, Cortese, R, Ciliberto, G and LaMonica, N ‘Site specific integration in mammalian cells mediated by a new hybrid baculovirus-adeno-associated virus vector’ 1998 J Virol 72,5025-34.

Joe Cummins is Professor Emeritus of genetics at the University of Western Ontario.

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