Do vaccines contain aborted fetal cells?
The short answer is: Yes, some do, but not all. I’ve heard a lot of people actually argue about this. Some people will argue emphatically and call you an idiot if you truly believe the “conspiracy theory” that vaccines contain aborted fetal cells. These people have clearly never bothered to read the list of ingredients printed in the vaccine package inserts. Nor have they visited the CDC website where aborted fetal cells are listed in the ingredients lists of various vaccines.
I don’t know, maybe it’s because they are looking for the words, “aborted fetal cells” which obviously aren’t there. It takes a little reading into the subject to discover that the words you should be looking for are “human diploid fibroblast cell structures” (which come in two strains- WI-38 and MRC-5).
The following vaccines were developed using one of the two aborted fetal strains above and do contain DNA from them:
- Hepatitis A
- Rubella (Rubella is a part of the MMR combination vaccine)
- Varicella (chicken pox)
- Zoster (shingles)
- Enbrel (Rheumatoid Arthritis)
The following vaccines that are in development come from additional aborted fetal strains and contain DNA:
- Flu and Avian Flu
Why are aborted babies needed to produce these vaccines?
In order to make a vaccine, scientists must be able to grow the bacteria or virus they wish to create a vaccine for. In order to grow the bacteria or virus, they must have tissue to grow it on. While many vaccines are created using the tissue of various animals (cows, monkeys, chickens to name a few) and animal products (such as eggs), the use of tissue from aborted babies is superior for a number of reasons.
*You can thank me later for posting a pic of an artist rendering instead of a photo…
First, vaccines derived from animal sources carry a higher risk of contamination from other bacteria and viruses. For example, the polio vaccines that our parents were vaccinated with in the 50’s and 60’s were later found to be contaminated with a monkey virus referred to as SV40 or Simian Virus 40. (Whoops!) Now, the CDC claims that SV40 didn’t cause any adverse effects. So, it’s very ironic that according to laboratory findings, “ SV40 DNA has been detected in several human tumors, including osteosarcoma, mesothelioma, and non-Hodgkin’s lymphoma. Similar tumors are induced by the virus in hamsters.” And no…the individuals whose tumors were found to contain SV40 DNA had no possible exposure to SV40 other than the polio vaccine. It’s not exactly something you come across on regular ole’ day in the US of A.
Second, some pathogens just don’t grow as well on animal tissue (like chicken pox) because they don’t infect animals. However, the most important advantage to using tissue from aborted babies is that fetal cells can go through many more divisions than other cells before they die. A biologist named Hayflick determined that normal human cells can only reproduce a finite number of times (usually around 50) before they stop reproducing. Fetal cells, however, are capable of going through many more divisions before dying.
Let’s get acquainted with the two aborted babies that the vaccines we inject our children with are grown on. (I sincerely hope that sentence makes you cringe as much I did when I typed it.)Believe it or not, the background information is actually available. WI-38 is a 3 month old female fetus who belonged to two married parents living in Stockholm, Sweden in 1962. Reportedly, her father was a “drunk” who was “gone a lot.” According to Dr. Rene Leive in her “Brief History of Human Diploid Strains,” her parents “felt they already had too many children”, so they decided to abort her. MRC-5 is a fourteen week old male fetus who was murdered inside his 27 year old mother in 1970 for “psychiatric reasons.”
Before we continue, let’s take a minute to see what a 15 week old baby (the average age of the aborted babies used to create these fetal strains) looks like in utero.
And here we come to the next misleading argument that is posited to rationalize or justify the use of aborted babies in the production of vaccines. If you’ll notice in the list of vaccine ingredients above, the vaccines that are currently in use today are all derived from two fetal cell strains: WI-38 and MRC-5. Our vaccines come from “only” two aborted babies. Again, Megan over at Whole Living puts it best with her “This Wasn’t Just a One-Night Stand” analogy, “You might have also heard that only two babies were used and it was a really long time ago, which justifies the continued use of shooting up live babies with dead babies.” Sometimes a little perspective goes a long way…
It may seem like common sense to some to realize that to arrive at WI number 38, numbers 1-37 logically preceded. You would be correct in this logical assumption. Hayflick also references WI-44 in his report, so you can be sure, very many more than one aborted baby has gone into the development of the WI-38 cell line that is still used today. The same holds true for the MRC-5 strain. Hayflick also makes mention of the MRC-9 strain which is derived from a 15 week old female fetus in 1974. Her mother was an unwed 14 year old who aborted her baby for “therapeutic” reasons according to the documentation (taken from the history of diploid strains linked above).
Our Rubella vaccine comes from another cell line, RA 27/3, which was developed by a man named Plotkin. It is derived from a female fetus whose mother contracted Rubella in 1964. She was aborted for this reason (rubella is only harmful to babies in utero and causes some severe birth defects). According to Plotkin’s documentation, over 40 aborted babies were cultured. RA 27/3 was not the first fetus to test positive for Rubella or the last and he doesn’t specify why he continued with the series. Interestingly, Dr. Leive notes, “It is documented that there were other effective virus strains already made at the time which had been obtained from other non-abortion-related methods.”
Can We Use These Same Cell Lines Forever?
No. They aren’t immortal and they’ll eventually die out. Scientists have never stopped developing new strains and new vaccines. In fact, they already have new human diploid cell strains to back up the current strains. IMR-90 is a 16 week old fetus from a 38 year old mother of six who decided the baby she was carrying in 1975 would be too inconvenient. Cell strain 293 is derived from kidney cells from a baby aborted in 1972. The PER C6 line, which is being used right now to develop the new ebola, flu, malaria, tuberculosis, and HIV vaccines, is derived from an 18 week old fetus aborted in 1985. The main researcher for the PER C6 line, Van der Eb, stated that, “the woman wanted to get rid of the fetus and the father was unkown.”
In fact, the American Congress of Obstetricians and Gynecologists is “distressed” that Congress is investigating fetal tissue researchers and procurement companies to make sure they aren’t profiting from the sale of tissue from aborted babies (which is illegal.) They released this statement, “Unfortunately, some state and federal politicians are working hard to obstruct- or even criminalize- fetal tissue research, limiting the ability of America’s leading scientists and researchers to develop new vaccines and medicines to prevent and treat disease. The ACOG warns that if this interference continues, “fetal research bans will stymie US based medical progress, leaving us to rely on other countries to develop medicines for our own patients.”
Apparently, without legal abortion to provide the scientific community with an endless supply of murdered babies, medical progress will virtually cease. Eye opening statement to say the least. There are some powerful players backing the pro-choice movement and their motivation has very little to do with a woman’s “right to choose.”
I’ll end with one last quote from Megan at Whole Living, “If science can’t advance without abortions, we need to go back to the drawing board.”
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