According to the Australian Immunisation Handbook, several vaccines licensed in Australia utilise human diploid cells derived from aborted foetal tissue (WI-38, MRC-5) in the manufacturing process.
Winstar Institute 38 (WI-38) – human diploid lung fibroblasts were derived from the lung tissues of a female fetus aborted because the family felt they had too many children in 1964 in the United States.
Medical Research Council 5 (MRC-5) – human diploid cells (cells containing two sets of chromosomes) were derived from the normal lung tissues of a 14-week-old male fetus aborted for “psychiatric reasons” in 1966 in the United Kingdom,
McCullagh (1987) reported on one of the methods used in harvesting foetal tissue in Sweden.
They would puncture the sac of a pregnant woman at 14 to 16 weeks, put a clamp on the head of the baby, pull the head down into the neck of the womb, drill a hole into the baby’s head and attach a suction machine to remove the brain cells… At 16 to 21 weeks, they would do prostaglandin abortions where a chemical is injected into the womb causing the woman to go into a mini-labor and pass the baby. Fifty percent of the time, the baby would be born alive, but that didn’t stop them. They would simply open up the abdomen of the baby with no anesthesia, and take out the liver and kidneys, etc.
Make no mistake. The abortions were done this way to ensure intact organs and tissue for research.
Due to dwindling capacity for existing aborted fetal cell lines to self-replicate, scientists in China have developed a new aborted fetal cell line, WALVAX 2 that will be used for viral vaccine production. The existing cell lines, MRC-5 and WI-38 are currently used in MMR, Varicella, Hepatitis-A, Shingles, some rabies and some polio vaccines.
WALVAX 2 is taken from the lung tissue of a 3 month gestation female who was ultimately selected from among 9 aborted babies. The scientists noted how they followed specific guidelines to mimic WI-38 and MRC-5 in selecting the aborted babies, ranging from 2-4 months gestation. They further noted how they induced labor using a “water bag” abortion to shorten the delivery time and prevent the death of the fetus to ensure live intact organs which were immediately sent to the labs for cell preparation.
According to the studies published earlier this year in the NIH Pub Med, scientists noted that Walvax-2 cells replicated more rapidly than MRC-5 cells, attained greater population doubling and performed better or equal to the existing cell lines for culturing viruses.
In 1964 Leonard Hayflick introduced what is known as the “Hayflick limit” – how all normal cells have a finite lifespan and limited capacity to replicate before going into senescence and eventually, become unstable and form tumors. (L. Hayflick, The Limited In Vitro Lifetime of Human Diploid Cell Strains, Experimental Cell Research, Vol 37, 1964) Attempts to immortalize these cells to extend their lifespan have likewise introduced problems with tumor formations, as in aborted fetal cell line PER C6, introduced into the US in 2001.
Such seems to be the case with the introduction of WALVAX 2 to replace Hayflick’s WI-38 and Medical Research Council’s MRC-5. But instead of choosing from several WHO and FDA approved moral cell line to replace them, they are using a new aborted fetal source.
“This is exactly what we have been saying for years,” stated Debi Vinnedge, Executive Director for Children of God for Life an organization that has been monitoring the use of aborted fetal materials in vaccines and other consumer products. “The pharmaceutical industry is not going to change their use of aborted fetal cells when they have tacit approval from our moral and medical leaders.”
For decades both the pharmaceutical companies and even some ethicists have insisted that the abortions to produce the cell lines used in vaccines were not done with that intention, that it was only a couple of abortions from the past and that no further abortions would be needed “now or in the future” to produce vaccines.
While Children of God for Life has been trying to expose these truths for the past 15 years , those warnings are now ringing startling accurate as evidenced with the recent Planned Parenthood videos that have emerged through the Center for Medical Progress, (CMP) showing how live, fully intact fetuses have been harvested for aborted fetal research.
And while Planned Parenthood has tried to claim the videos are doctored and they have done nothing wrong, in reality the facts supporting the CMP evidence is not only damning it has been fully documented in numerous science publications on vaccine research for the past 85 years.
With concern rising, some have gone so far as to patently state that the cells used are really only “descendant ” or “daughter” cells that are actually no longer a part of the original aborted fetus. Vinnedge is quick to point out that this too is nothing more than a pathetic attempt to placate concerned parents.
“Anyone with even a cursory knowledge of Biology 101 knows that the cells from a human being do not morph into something different over time, ” she stated. “Further, from FDA safety standards, no human diploid cell line could be used for vaccine production on an ongoing basis if the cells somehow transformed or the DNA from that original aborted child was not fully and genetically intact.”
“But once those cells reach their finite capacity for replication, they will eventually become unfit for vaccine production and another cell line will be needed.
“Unfortunately, their selected of replacement using a new aborted fetal source is not good news for concerned parents, physicians and pro-life leaders,” she added.
You can also watch the video below of Marcella presenting this to an Atlanta audience.
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