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Lifenotes
Vaccines, Abortion, & Fetal Tissue
For several years now, information has circulated among prolife
groups and individuals regarding the development of very common
vaccines through the use of tissue taken from aborted babies.
While initially the reports and information were not conclusively
documented, further detailed research by several prolife groups
has provided direct proof of a connection between aborted fetal
tissue and most vaccines. That connection, and its implications
for whether prolife citizens should consider using the vaccines,
raises some complicated issues. In sorting through those issues,
this LifeNotes will address the basic science involved, the documentation
of the abortion-vaccine connection, the moral/ethical questions
about using abortion-tainted vaccines, and information about available
alternative vaccines.
Basic Vaccine and Cell Line Science
The vaccine process works by collecting samples of the actual
virus, then growing and altering them in the laboratory to make
a weakened strain of the disease. That weakened strain is put
into a serum and administered into the body (usually by injection).
The body's immune system is more capable of naturally attacking
and destroying the weakened virus, and thus develops the ability
to effectively fight off the actual disease should the person
ever be exposed to it. The advent of vaccines was a major milestone
in medicine, saving millions of lives and saving many others from
the devastating effects of diseases like polio.
In order to develop the weakened viral strain, there must be
a medium or "cell culture" to grow it in. The virus
invades the culture cells, feeds off the cell, matures, and multiplies.
The cell cultures are a single type of cell that multiplies itself
in a predictable fashion and can be sustained in a laboratory
setting for years, even decades. These long-lasting cell cultures
are called "cell lines." The original cells that start
these cell lines have been taken from a wide variety of sources,
from monkey embryo and kidney cells, to chicken and rabbit embryos,
and tragically, from aborted human babies. The issue of concern
is that many common vaccines were developed using cell lines that
originally were cells taken from electively aborted babies. The
vaccines themselves do not contain fetal cells, but it is presumed
that there is "residual" biological matter from the
fetal cells that has been assimilated into the vaccine.
Cell Lines Originating from Aborted Babies
There are two particular fetal cell lines that have been heavily
used in vaccine development. They are named according to the laboratory
facilities where they were developed. One cell line is known as
WI-38, developed at the Wistar Institute in Philadelphia, PA.
The other is MRC-5, developed for the Medical Research Council
in England. WI-38 was developed by Dr. Leonard Hayflick in 1962,
by taking lung cells from an aborted female baby at approximately
the end of the third month of pregnancy. Dr. Hayflick's article
published in the scientific journal, Experimental Cell Research states that three cell lines, WI-26, WI-38, WI-44 were all developed
from aborted babies. "All embryos were obtained from surgical
abortions and were of approximately three months' gestation1." In another journal article (American Journal of Diseases
of Childhood) from an international conference on Rubella,
Dr. Stanley Plotkin who developed a Rubella vaccine using WI-38,
addressed a question as to the origin of WI-38. Dr. Plotkin stated, "This fetus was chosen by Dr. Sven Gard, specifically for
this purpose. Both parents are known, and unfortunately for the
story, they are married to each other, still alive and well, and
living in Stockholm, presumably. The abortion was done because
they felt they had too many children. There were no familial diseases
in the history of either parent, and no history of cancer specifically
in the families2."
The origin of the MCR-5 cell line, created in 1966, is documented
in an article in the journal Nature by three British
researchers working at the National Institute for Medical Research.
J.P. Jacobs, et. al. write, "We have developed another strain
of cells, also derived from foetal lung tissue, taken from a 14-week
male foetus removed for psychiatric reasons from a 27 year old
woman with a genetically normal family history and no sign of
neoplastic disease both at abortion and for at least three years
afterward3." Noting that their research parallels that of
Dr. Hayflick's development of the WI-38 cell line, the researchers
conclude, "Our studies indicate that by presently accepted
criteria, MRC-5 cells - in common with WI-38 cells of similar
origin - have normal characteristics and so could be used for
the same purposes as WI-38 cells4."
In both of these cell lines it is quite clear that the aborted
children were presumed to be healthy, and that there was no life-threatening
condition or other medically indicated reason for the abortion
of these two babies.
There is a more recent cell line, PER C6, developed in 1985,
which is being used currently in research to develop vaccines
to treat Ebola and HIV. The origin of PER C6 is clearly documented.
In direct testimony before the Food and Drug Administration's
Vaccines and Related Biological Products Advisory Committee, Dr.
Alex Van Der Eb, the scientist who developed PER C6, stated:
"So I isolated retina [cells] from a fetus, from a healthy
fetus as far as could be seen, of 18 weeks old. There was nothing
special in the family history, or the pregnancy was completely
normal up to the 18 weeks, and it turned out to be a socially
indicated abortus, abortus provocatus, and that was simply because
the woman wanted to get rid of the fetus5."
To date, no vaccines have been successfully marketed using the
PER C6 cell line, but undoubtedly the cells used to establish
PER C6 came from a healthy baby, aborted from a healthy mother
for social convenience reasons. While most of the common childhood
vaccines used today were developed using the WI-38 and MRC-5 fetal
cell lines, there are some vaccines available that were developed
using animal cell lines. The tables on the following page indicate
the abortion-tainted vaccines, and the available alternatives.
U.S. Produced
Vaccines from Aborted Cell Lines
| Disease |
Vaccine Name |
Manufacturer |
Cell line (fetal) |
| Polio |
Poliovax |
Aventis-Pasteur |
MRC-5 |
| Rabies |
Imovax |
Aventis-Pasteur |
MRC-5 |
| Hepatitis A |
Havrix |
Merck & Co. |
MRC-5 |
|
Hepatitis A |
Vaqta |
Glaxo/SmithKline |
MRC-5 |
| Hepatitis A-B Combo |
Twinrix |
Glaxo/SmithKline |
MRC-5 |
| Smallpox |
Acambis 1000 |
Acambis |
MRC-5 |
| Chickenpox |
Varivax |
Merck & Co. |
MRC-5/WI-38 |
| Measles, Mumps, Rubella |
MMR II |
Merck & Co |
WI-38 |
| Mumps-Rubella |
Biavax II |
Merck & Co |
WI-38 |
| Measles-Rubella |
MR-VAX |
Merck & Co |
WI-38 |
| Rubella only |
Meruvax II |
Merck & Co |
WI-38 |
U.S. Produced Alternative
Vaccines
(There are no U.S. alternatives for Chickenpox, Rubella, Hepatitis-A)
| Disease |
Vaccine Name |
Manufacturer |
Cell line |
| Polio |
IPOL |
Aventis-Pasteur |
Monkey kidney |
| Mumps |
Mumpsvax |
Merck & Co. |
Chick embryo |
| Measles |
Attenuvax |
Merck & Co. |
Chick embryo |
| Rabies |
RabAvert |
Chiron Therapeutics |
Chick embryo |
|
Smallpox
Hepatitis B |
Acambis 2000
Engerix, Comvax
|
Acambis-Baxter
Glaxo/Smith/Kline, Merck
|
Monkey kidney
Yeast
|
There are Japanese produced alternative vaccines for Rubella
and Hepatitis-A, developed from cell lines of rabbit and monkey
kidney. These vaccines are available in the U.K., but have not
yet been given FDA approval for use in the U.S. If these two alternatives
were to become available in the U.S., then Chickenpox would be
the only abortion-tainted vaccine without an acceptable alternative.
Should These Vaccines Be Used? The Moral & Ethical Considerations
The ethical quandary created by the tainting of these otherwise
beneficial vaccines is obvious and vexing. Parents are more than
justified in wanting to protect their children from these potentially
life-threatening diseases. It can be legitimately argued that
parents have an obligation to take reasonable steps to protect
their children. Likewise, as a society, we must take into consideration
the morality and cost of failing to prevent widespread outbreaks
of disease. Thus, there is a civic responsibility associated with
vaccines and controlling diseases.
The moral perspective of those who are utterly opposed to the
use of these vaccines is straightforward and equally justifiable.
If these vaccines were developed from cell lines taken from Jews
murdered in Nazi concentration camps, it is not difficult to imagine
that there would be widespread, if not universal rejection of
those vaccines. Since many prolifers see no difference between
the moral magnitude of abortion and the Holocaust, their passionate
refusal to use these vaccines is completely understandable.
When dealing with difficult ethical issues like vaccines grown on the tissue of aborted children, one of the main questions to answer is how do individuals act in a moral way when they are acting in a world that is filled with immorality. For example, should a person watch no television programming on a certain network because some of its programming is immoral? It is crucial to remember that the moral nature of any act depends first on the action itself. Secondly, the intention of the individual is also a crucial factor. The further away the current act (using a vaccine) and intent (protecting a child from a disease) of an individual are from a previous immoral act (aborting a child), the less that individual is restricted by the immorality of the previous act. While the act of aborting the child was certainly immoral, all of the steps involved with the development and use of the vaccines thereafter neither cooperated with the abortion, nor intended to promote more such practices, nor intended anything but the preservation of life and health.
The Vatican's Pontifical Academy for Life, and the U.S. and British bishops conferences have studied the issue in detail and concluded that using the vaccines is morally permissible. However, once a person learns that certain vaccines are morally tainted, there is an obligation to seek out ethical alternatives where possible and to make objections known to health care providers and vaccine manufacturers. In addition, parents are entirely justified in citing a "conscientious objection" to tainted vaccines being used to immunize their children, particularly when the vaccine is not for a substantially threatening illness (Chickenpox, flu). Parents have a right to demand ethical alternatives be used or reject the vaccine if an alternative is not available.
A number of noted prolife activists have weighed in on both sides
of the issue. Some have
encouraged parents to use and demand nothing less than morally
acceptable vaccines 7. While others like Jack Wilke, M.D., former National Right to Life Committee president and Bernard Nathanson, M.D., prolife activist and creator of “The Silent Scream” have opined that using the vaccines is morally allowable 7,8.
What is unanimous among all commentators on the subject is that
everyone ought to know of the facts surrounding the vaccines,
and prolife citizens should make an effort to persuade - even
pressure - vaccine producers to eliminate their tainted products
in favor of ethically acceptable products.
Vaccines & Bioterrorism
An additional concern related to vaccine use is the post-September
11 concern about bioterrorist threats using agents such as Anthrax
or Smallpox. President Bush has ordered the mass production of
Smallpox vaccines, and vaccination for himself and most military
personnel. In the event of an attack using Smallpox, large numbers
of the public would be able to access a protective vaccination.
As part of the initial order for millions of doses of Smallpox
vaccine to be created, 50,000 doses of Acambis 1000 (abortion
tainted) were secured. When the abortion connection was brought
to HHS Secretary Tommy Thompson, he instructed that the additional
millions of doses to be created should use either Acambis 2000
(abortion free) or possibly a European vaccine that is also abortion
free. Thus, out of tens of millions of doses of Smallpox vaccine
to be created, utilized, or stored, less than 1/10 of 1% will
be the abortion tainted version.
References
1 Hayflick, L, et. al. "The Limited In Vitro
Lifetime of Human Diploid Cell Strains," Experimental Cell Research,
Vol 37, 1965, p. 615.
2 Statement
by Dr. Stanley Plotkin published in "Gamma Globulin Prophylaxis;
Inactivated Rubella Virus; Production and Biological Control of Live
Attenuated Rubella Virus Vaccines," American Journal of Diseases
of Childhood, Vol. 118, No. 2, 1969, p. 378.
3 Jacobs,
J.P., et. al., "Characteristics of a Human Diploid Cell Designated
MRC-5," Nature, Vol. 227, 1970, p. 168.
4 Ibid,
p. 170.
5 Transcript
of the Vaccines and Related Biological Products Advisory Committee of
the U.S.Food and Drug Administration, hearing date May 16, 2001, Gaithersburg,
MD, p.91.
6 Brown,
Judie, President, American Life League, in a letter to the National
Catholic Register, April 30-May 6, 2000.
7 Wilke,
J.C., M.D., "Vaccines, Today's Controversy," Life Issues Connector,
Life Issues Institute, Cincinnati, OH, July, 2001.
8 Nathanson,
Bernard, M.D., "Vaccines OK'd Despite Dark Past," National
Catholic Register, June 18-24, 2000.
Produced by: Right to Life of Michigan PO Box 901
Grand Rapids MI 49509 www.rtl.org
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