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This new form of treatment might benefit millions
EDITOR Nevertheless, as with almost every medical or scientific advance,
it will be impossible to exclude all risk, even if this is related only
to hitherto unknown pig bacteria or viruses. The ultimate decision
whether to use any new therapeutic agent or procedure rests on an
assessment of the risk to benefit ratio. As the potential benefits to
individuals or society increase, the acceptance of slightly increased
risk becomes warranted. We must not reduce our obligation to take all
possible steps to minimise any perceived risk to society, but we have a
moral obligation to accept a small risk to the community if the new
treatment leads to great benefit to many individuals in that community.
The potential benefits of xenotransplantation are immense. Many
millions of people with such diverse conditions as diabetes and
degenerative brain disease may have the quality of their lives vastly
improved, and in those with advanced organ failure xenotransplantation will be lifesaving. In the United States over 60 000 people currently await a human donor organ but only 20 000 organs will become available this year. At least 10 people die every day while waiting. Similar figures could be quoted for other regions of the developed world.
This new form of treatment may ultimately benefit millions of patients.
Rather than calling for a ban on it we suggest that support should be
given to the great efforts being made to ensure that it will be not
only successful but also safe.
Fano has written a response in the eBMJ (and
published here, the third letter) commenting on Vanderpool's article
on xenotransplantation.
1 2
He advocates a ban on
xenotransplantation, largely on the grounds of the risk of the transfer
of infection. Cells taken from carefully screened pigs have been used
in the treatment of patients with diabetes, certain neurological
diseases, and liver failure. There has been no definite evidence of the transfer of a porcine infection to human recipients.
Massachusetts General Hospital, 13th Street, Boston, MA 02129, USA cooper{at}helix.mgh.harvard.edu
Carl G Groth
Huddinge Hospital, Huddinge S-14186, Sweden
Ian F C McKenzie
Austin Research Institute, Austin and Repatriation Hospital,
Heidelberg, Victoria, Australia
| 1. |
Vanderpool HY.
Xenotransplantation: progress and promise.
BMJ
1999;
319:
1311 |
| 2. | Fano A. Xenotransplantation: perils and plagues. eBMJ 1999. (www.bmj.com/cgi/eletters/319/7220/1311#EL2). |
Public health risk must not be dismissed
EDITOR Viruses that inhabit animals, some of which are intrinsic to the
animal's own genome, will gain a route of entry into the human
population not ordinarily available. As Vanderpool notes,1 pig DNA contains endogenous retroviruses (the same class that causes
AIDS), and these infect human tissue culture cells.2 Vanderpool doesn't mention that postmortem analyses of two patients who died 70 and 27 days after receiving baboon livers showed two simian
viruses that replicated after transplantation.3 Our state
of knowledge is far too incomplete for us to breed totally virus-free
animals, because we probably don't even know all the viruses that need
to be eliminated.
We do know that viruses jump species even without our help, and there
are enough frightening precedents The spectacular advance of AIDS resulted from a virus given new routes
of entry: widespread increases in certain lifestyle practices provided
a conduit for efficient transmission. HIV-1 probably also resulted from
a simian to human virus jump. Deadly Ebola virus is another virus
transmitted to humans from primates, and there are at least another 10 primate viruses that infect humans, including a deadly form of herpes.
Pigs aren't much safer: about a dozen pig viruses can be transmitted
to humans, often with serious results.
Not considered by Vanderpool is the fact that better alternatives
exist. These include lifestyle changes (diet and exercise) that would
considerably reduce the numbers of transplant candidates and presumed
consent policies for human donors, which would greatly expand the pool
of available organs. Research on unwanted human embryos is much more
promising as a solution, but this is held hostage to abortion politics
in the United States. Instead we are absurdly rushing down a path
fraught with danger. Have we learnt nothing from the AIDS epidemic?
Research in xenotransplantation will line drug industry's
pockets
EDITOR Given the multitude of viruses lurking in animals, it will be
impossible to breed germ free "donors." Public health authorities admit that xenotransplantation could transmit deadly animal viruses to
humans. Known pig viruses include the porcine endogenous retroviruses that have infected human cells. In 1998-9 the Malaysian Nipah virus
causing viral encephalitis jumped from pigs to humans, infected 269 people, killed over 100, left dozens brain damaged, and led to the mass
slaughter of one million pigs. Pig viruses have not been extensively
studied: there may be dozens, many with long latency periods, waiting
to be discovered.
A retrospective study of 160 patients exposed to living pig
tissue raised concerns3: 30 patients who underwent splenic perfusions gave positive results when tested for porcine endogenous retrovirus DNA; 23 had pig cells circulating in their bodies 8.5 years
after treatment; and four injected with pig cells produced antibodies
to porcine endogenous retroviruses, suggesting a potential active
infection. The study's sponsor, Novartis, insists that patients are
free of infection. But virologist Stoye and coauthors have said "the
absence of infectious virus in, say, the first two hundred patients
does not mean it will not occur in the two hundred and
first."4
I am baffled as to why our public health authorities, mandated to
protect public health and prevent disease, are encouraging the
development of xenotransplantation while simultaneously acknowledging its epidemic potential. This could become a liability for them.
In 1998 a group of physicians pointed out that global poverty (and lack
of access to basic health care and sanitation) is the world's number
one health problem.5 Today, some 50 million Americans lack
access to basic health care. If we invest in xenotransplantation while
ignoring the fundamental needs of a majority of the world's citizens
we are simply lining the drug industry's pockets.
Author's reply
EDITOR Goldman warns that the public health risk of xenotransplantation
"must not be dismissed," which no one seems to be doing. Goldman's
points about the known infectivity of simian viruses have, as my
article says, already been taken to heart by the United States Food and
Drug Administration, which suspended clinical research involving
primate-to-human xenografts.
Goldman ends with a list of better alternatives to xenotransplants.
Better for whom and how soon? Lifestyle changes would reduce the demand
for transplanted organs, but they will neither end this demand nor be
voluntarily and universally adopted. Presumed consent would expand the
organ donor pool, but it is a form of coercion that would also not meet
the great demand.
Fano expresses the party line of the Campaign for Responsible
Transplantation, which he directs and which claims to represent 2.5 million members. The campaign's publications advocate an immediate ban
on xenotransplantation and charge the Food and Drug Administration with
"playing Russian roulette with the public's
health."1
Fano holds that xenotransplantation is being advanced to line "the
drug industry's pockets," not to alleviate human suffering. While
few will quarrel with the influence, if not the necessity, of the
profit motive, numerous researchers, surgeons, scientists, and
regulators are additionally, and sometimes primarily, motivated by
altruism, inquisitiveness, discovery, and the classic three factors in
the Hippocratic oath: honour, fame, and enjoyment of life.
Fano is baffled that public health authorities are encouraging the
development of xenotransplantation in the light of its epidemic
potential. His evidence for this potential with respect to clinical
trials of xenotransplantation is attributed to a study that does not
support his fears.2
This study further validates other findings that persistent porcine
endogenous retrovirus infection has not been detected in recipients of
xenotransplants. The 30 (of a total of 160) patients that Fano refers
to as testing positive for persistent porcine endogenous retrovirus
evidenced microchimerism (the remaining presence of pig cells in their
bodies), not persistent porcine endogenous retrovirus infection.
Xenotransplantation of organs from animals is a seductive but
inherently dangerous idea. The risk is not just to the patient, who
will probably die shortly afterwards; the stakes are much higher,
because the entire human population is put at risk.
as far back as the 1918 swine
influenza pandemic that killed 20 million
to scare anyone
contemplating xenotransplantation. More recently, millions of chickens
had to be slaughtered in Hong Kong because of the unexpected jump to
humans of an avian influenza virus, and thousands of English cattle
have been destroyed because of the jump to humans of bovine spongiform
encephalopathy ("mad cow disease").
Department of Microbiology and Molecular Genetics, New
Jersey Medical School - UMDNJ, 185 South Orange Avenue, Newark, NJ
07103, USA egoldman{at}umdnj.edu
1.
Vanderpool HY.
Xenotransplantation: progress and promise.
BMJ
1999;
319:
1311. (13 November.)
2.
Patience C, Takeuchi Y, Weiss RA.
Infection of human cells by an endogenous retrovirus of pigs.
Nature Med
1997;
3:
282-286[CrossRef][Medline].
3.
Allan JS, Broussard SR, Michaels MG, Starzl TE, Leighton KL, Whitehead EM, et al.
Amplification of simian retroviral sequences from human recipients of baboon liver transplants.
AIDS Res Hum Retroviruses
1998;
14:
821-824[Medline].
It is naive to believe that research in
xenotransplantation "is being propelled" by drug companies' desire
to alleviate human suffering rather than the promise of billions of
dollars in profits from the sale of "humanised" pig parts and
expensive antirejection drugs.1 There would be safer and
more cost effective ways of dealing with the perceived shortage of
human organs and tissue. Aggressive investment in programmes to prevent
disease; the passage of "presumed consent" laws, which have
increased organ donation rates in several countries2; and
growing human tissue to provide a safer source than animals would all help.
Campaign for Responsible Transplantation, PO Box 2751, New York, NY 10163, USA alixfano{at}mindspring.com
1.
Vanderpool HY.
Xenotransplantation: progress and promise.
BMJ
1999;
319:
1311. (13 November.)
2.
Kennedy I, Sells RA, Daar AS, Guttmann RD, Hoffenberg R, Lock M, et al.
The case for "presumed consent" in organ donation.
Lancet
1998;
351:
1650-1652[CrossRef][Medline].
3.
Paradis K, Langford G, Long Z, Heneine W, Sandstrom P, Switzer WM, et al.
Search for cross-species transmission of porcine endogenous retrovirus in patients treated with living pig tissue.
Science
1999;
285:
1236-1241 4.
Stoye JP, Le Tissier P, Takeuchi Y, Patience C, Weiss RA.
Endogenous retroviruses: a potential problem for xenotransplantation.
Ann NY Acad Sci
1998;
862:
73.
5.
Guerrero R, Jancloes M, Martin JD, Haines A, Kaseje D, Wasserman MP.
How the cycle of poverty and ill health can be broken.
BMJ
1998;
316:
1456
Cooper et al's letter is commendable. Research on porcine
cells, tissues, and organs in xenotransplantation should continue if
certain conditions are met. There should be ongoing studies of risks
and increased recognition that xenotransplantation offers enormous
potential for alleviating human sickness, suffering, and untimely
death. To assume that xenotransplantation must be free of risk before
its benefits are pursued is out of keeping with the nature of human
existence and represents a preoccupation with self protection that
undermines beneficence.
Institute for the Medical Humanities, University of Texas
Medical Branch, Galveston, TX 77555, USA hvanderp{at}utmb.edu
1.
Fano A.
CRT: re Docket N. 99D-5347: precautionary measures to reduce the possible risk of transmission of zoonoses.
New York: Campaign for Responsible Transplantation, 2000:12.
2.
Paradis K, Langford G, Long Z, Heneine W, Sandstrom P, Switzer WM, et al.
Research for cross-species transmission of porcine endogenous retrovirus in patients treated with living pig tissue.
Science
1999;
285:
1236-1241.
© BMJ 2000
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