Do vaccines actually contain aborted human fetal tissue?
It seems the majority of pro-vaccine advocates in the community don’t realize, or have purposefully ignored the fact that the Measles, Mumps, Rubella (MMR) Vaccine contains aborted fetal tissue. As a Vaccine researcher in the field, I’m coming up against this obstacle almost every day now.
So let’s set the record straight.
Aborted human fetal (Diploid Cell) tissue is found in the Rubella portion of the MMR Vaccine formula – Note: ‘the Wistar RA 27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts (Aborted Human Fetal Tissue).’
Some in the community are still reluctant to admit they’ve been lied to for generations by so-called Government appointed health authorities. There is no safe threshold for any vaccines, whatsoever.
Measles, Mumps, Rubella Vaccine (series 1st round given at 12-15 months old) – Official Package Insert:
‘M-M-R II is a sterile lyophilized preparation of (1) ATTENUVAX* (Measles Virus Vaccine Live), a more attenuated line of measles virus, derived from Enders’ attenuated Edmonston strain and propagated in chick embryo cell culture; (2) MUMPSVAX* (Mumps Virus Vaccine Live), the Jeryl Lynn** (B level) strain of mumps virus propagated in chick embryo cell culture; and (3) MERUVAX* II (Rubella Virus Vaccine Live)…,‘
In case you missed that reference: ‘the Wistar RA 27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts.’
For those of you still in doubt, meet WI-38.
WI-38 came from lung cells from a female fetus of 3-months (terminated during the 1st Trimester) gestation: ‘Minced preparations were obtained by cutting the tissue in a Petri dish containing GM (growth medium) with paired scalpels or a scissors until the size of each piece approximated l-4 mm3. Fragmented preparations were obtained by tearing apart the tissue with two pairs of forceps in a Petri dish containing GM until the pieces could no longer conveniently be grasped and shredded.
The entire contents of the dish were emptied into one or more Pyrex Blake bottles (surface area 100 cmZ), depending on the size of the original starting tissue. The fragmented lungs, for example, from a three-month-old human fetus were usually placed in four Blake bottles. Treatment of tissue with trypsin was done, in general, according to the method of Fernandes.‘
Note: ‘Although it cannot be said with certainty that any cell line or cell strain is absolutely free of contaminating viruses our evidence does not suggest the presence of such viruses…The question of the presence of latent viruses in any cellular material is one that can probably never be answered with absolute certainty…‘
Outline of the standard procedure (serial cultivation) & inherent risks (malignant “contaminating viruses”) involved in procurement of aborted human fetal tissue:
Phase I, or early growth phase, constitutes that period when the cells have been freed from the intact tissue and are just establishing themselves on glass (primary culture). In general this phase lasts from 1 to 3 weeks.
Phase II is characterized by rapid cell multiplication and great acid production. During this phase the diploid strains must be subcultured at least twice a week with split ratios of ‘2 or 3: 1. This coincides with the formation of confluent sheets.
Phase III or the terminal phase, is characterized by the appearance of debris, reduction of mitotic activity and a consequently longer period of time for the development of confluent sheets…However, in interphase cells of Phase III, bizarre nuclear forms (“malignant” cancerous tissue) and sizes become more frequent and the appearance of these nuclei is reminiscent of irradiated cultures. Our attempts to reverse Phase III have been uniformly unsuccessful.
It is apparent…that by freezing cells (-70°Celsuis = -94° Farenheit) at each subcultivation or every few subcultivations one could have cells available at any given time and in almost limitless numbers.
‘The WI-38 and MRC-5 cell cultures have been used to prepare hundreds of millions of doses of (following) vaccines – rubella (third component of the MMR series, administered in 2 doses, first at 12 months old), hepatitis A (administered in 2 doses, first at 12 months old), varicella (chickenpox, administered in 2 doses, first at 12 months old) and rabies (administered selectively pending rabies-related emergency).‘ National Network for Immunization Information
According to the Vaccine Industry, material extracted from a human fetus aborted during the first trimester “does not and cannot form a complete organism and does not constitute a potential human being”. When a human life is cut short in utero, then reduced to “minced (meat) preparations of tissue in a Petri dish”…”torn apart with two pairs of forceps until the pieces could no longer conveniently be grasped and shredded”, labelled as “cell strains (which) do not and cannot form a complete organism and do not constitute a potential human being”, all in the name of scientific progress, you know something is definitely wrong with the ethical parameters supporting Modern Medical research.
The Rubella Vaccine strain (RA 27/3) found in the current MMR Vaccine on the market originally derived from a stockpile of 27 human fetuses, acquired during the Rubella Epidemic of 1964 – all contaminated with the Rubella virus (German Measles). “Infected Kidney ‘Fibroblast cells” were extracted from the third specimen, which were then subcultivated, after which ‘the supernatant fluid (surface liquid after it has been centrifuged) was inoculated directly into a WI-38 culture (aborted human fetal tissue). Once transferred to WI-38, the RA 27/3 rubella strain was passaged further in the same cell strain.‘
Consequently, the Measles, Mumps, Rubella (MMR) Vaccine is laced with the contaminated remains of two aborted human fetuses – surface liquid extracted from a Rubella virus-infected kidney (RA 27/3) combined with intrauterine-infected lung tissue from a second fetus (WI-38). ‘Thus, rising autistic disorder prevalence is directly related to vaccines manufactured using human fetal cell lines.‘
Note: Preliminary testing of the Frankenstein concoction was conducted upon “institutionalized children“, who were force-vaccinated, to observe the results – another crime against the innocent & defenceless, swept under the carpet by an Industry bent on greed & profits.
Mother & baby-to-be share the same Immune System, during all three trimesters, while the Fetus is ‘in Utero’, via the Placenta. Those young parents who oppose vaccinations (ie. the MMR Vaccine) for their family, based primarily on Religious convictions, demonstrate a wisdom beyond their years, trusting in the body’s innate capacity to overcome (adapt to) viral infections, such as Measles, through natural exposure in the environment.
They also recognize that it is fundamentally unscientific, let alone unethical, to inject aborted fetal tissue, laced in the MMR Vaccine, into a child’s bloodstream. Whether you profess science or faith as your reasoning behind that ultimate conclusion, the bottom line, those with Religious convictions, who choose to maintain a vaccine-free lifestyle, have seen the light.
Human Diploid Cells (aborted fetal tissue) provide the “Cell culture” in which vaccine formulas are often grown or nurtured. Current vaccines in circulation which contain aborted fetal tissue include:
1. Polio vaccine (inactivated/IPV) & Oral Polio (live virus) drops
2. Measles, Mumps, Rubella vaccine/MMR (Rubella component)
3. Diphtheria, Tetanus, Pertussis, Poliomyelitis vaccine (DTaP/TdP)
4. Varicella (Chickenpox) vaccine & Shingles (zoster) vaccine
5. Hepatitis A vaccine
6. Rabies vaccine
‘Some vaccines—rubella, HepA, RAB-HDC, VAR, ZOS, and one form of IPV (the Poliovax contained in Pentacel)—are grown in cultured human embryo fibroblast cell lines (WI-38 or MRC-5) because these are the only cells that replicate the viruses in high enough titer for mass production (the rubella vaccine strain itself was originally isolated from an aborted fetus with intrauterine infection).‘ Monthly Prescribing Reference (MPR) – Medical Industry Reference Journal
‘Today, more than 23 vaccines are contaminated by the use of aborted fetal cells. There is no law that requires that consumers be informed that some vaccines are made using aborted fetal cells and contain residual aborted fetal DNA. While newer vaccines produced using aborted fetal cells do inform consumers, in their package inserts, that the vaccines contain contaminating DNA from the cell used to produce the vaccine, they do not identify the cells as being derived from electively aborted human fetuses.‘ Dr. Theresa A. Deisher, Ph.D.
‘Not only damaged human cells, but also healthy human cells can take up foreign DNA spontaneously. Foreign human DNA taken up by human cells will be transported into nuclei and be integrated into host genome, which will cause phenotype change. Hence, residual human fetal DNA fragments in vaccine can be one of causes of autism spectrum disorder in children through vaccination.‘ Spontaneous Integration of Human DNA Fragments into Host – Dr. Genome K. Koyama, Dr. Theresa. A. Deisher Ph.D.
Study findings: ‘In addition to the ingredients listed on the package insert for Meruvax II® (Rubella virus vaccine live), we detected significant levels of human ssDNA (142 ± 8 ng/vial) as well as dsDNA (35 ± 10 ng/vial) fragmented to -215 base pairs in length. The MMR II® package insert discloses the presence of human fetal residuals nor how much cell substrate dsDNA (double-stranded DNA) or ssDNA (single-stranded DNA) contaminates each dose.‘ Journal of Public Health and Epidemiology, 09/2014
Note: ng = nanogram (one billionth of a gram)
‘The children vaccinated with MMRII, Varicella and Hepatitis A vaccines varied from 19 to 35 months of age at the time of vaccination. Autistic disorder birth year change-points (sudden spike in cases) were identified as 1980.9, 1988.4 and 1996 for the US, 1987 for the UK, 1990.4 for Western Australia, and 1987.5 for Denmark.
Change points in these countries corresponded to introduction of or increased doses of human fetal cell line-manufactured vaccines…Further, linear regression revealed that Varicella and Hepatitis A immunization coverage was significantly correlated to autistic disorder cases.’
Note: ‘Autistic disorder change points years are coincident with introduction of vaccines manufactured using human fetal cell lines, containing fetal and retroviral contaminants, into childhood vaccine regimens. Thus, rising autistic disorder prevalence is directly related to vaccines manufactured using human fetal cell lines.‘
Note: The aforementioned Study verifies that human DNA, the genetic template (blueprint) a child enters the world equipped with, which determines their capacity to thrive, can, in fact, be damaged, lessened, rendered defective AFTER birth, post-vaccination; blowing the entire CDC argument implicating genetics as the primary cause for Autism, completely out of the proverbial water.
All Standard Immunization-type vaccines in circulation requiring Human Diploid Cells (HDC), including those discontinued vaccines which utilized HDC since its inception in 1961, have derived the cell strain culture itself from one exclusive, carefully guarded “batch” or stockpile; comprising the fetal remains (lung tissue) of a female fetus of 3-months gestation (acquired in 1961/US), and those of a terminated 14-week-old male fetus (acquired in 1966/UK).
Human Fetal Links with Some Vaccines; ‘Human diploid cells are batches of human cells that are grown in a laboratory. Unlike cancer cells, they have the same number of chromosomes as normal human cells. Certain diploid cell strains are valuable in vaccine manufacture because these cells can be used for a very long period of time in the laboratory and are a reliable means by which many viruses that infect humans can be successfully and easily grown. Vaccines prepared in human diploid cells have proven to be very safe over the past several decades.
Two different strains of human diploid cell cultures made from fetuses have been used extensively for vaccine production for decades. One was developed in the United States in 1961 (called WI-38) and the other in the United Kingdom in 1966 (called MRC-5). WI-38 came from lung cells from a female fetus of 3-months gestation and MRC-5 was developed from lung cells from a 14-week-old male fetus. Both fetuses were intentionally aborted, but neither was aborted for the purpose of obtaining diploid cells.123. The fetal tissues that eventually became WI-38 and the MRC-5 cell cultures were removed from fetuses that were dead. The cellular biologists who made the cell cultures did not induce the abortions.
These two cell strains have been growing under laboratory conditions for more than 35 years. The cells are merely the biological system in which the viruses are grown. These cell strains do not and cannot form a complete organism and do not constitute a potential human being. The cells reproduce themselves, so there is no need to abort additional fetuses to sustain the culture supply. Viruses are collected from the diploid cell cultures and then processed further to produce the vaccine itself.’ National Network For Immunization Information
The introduction of Human Diploid Cells for use in Vaccine Technology followed closely on the heels of the disastrous Salk & Sabin Polio inoculation campaign; both in the United States (1954-55) and subsequently in Britain (1957). ‘The introduction of polio immunisation was accompanied by mass campaigns targeted at all individuals aged less than 40 years.‘
– a time-frame where-in either set of PARENTS from which the Human Diploid Cells specimens were acquired could obviously have been previously vaccinated with the Salk live Poliomavirus vaccine.
Therefore, the specimens which comprise the exclusive Human Diploid Cell culture stockpile may very well have “inadvertently” been co-infected with Simian Virus SV40 (diseased Rhesus & African Green Monkey tissue culture – strain utilized to nurture Poliomyelitis, hidden in the germ line DNA of either Fetus – the result of direct SV40 contamination from the Salk Vaccine (live Poliomavirus) co-infecting the DNA of either set of parents responsible for the baby’s genetic material now in widespread use; subsequently passed on from mother to Fetus via the Placenta.
An entire generation has since been inoculated with vaccines containing the original Human Diploid Cell culture set. If, indeed, there was any SV40 cross-contamination embedded in the lung tissue culture extracted from either Fetus, the primary HDC source in circulation, it is logical to determine that SV40 cross-contamination has also made its way into those who were subsequently vaccinated (intramuscularly, subcutaneously or via oral drops) with the same Human Diploid Cell culture source.
This would certainly explain the recent Controlled Study where-in Simian Virus co-infection was identified in 67% of post-mortem brains of sufferers of Autism.
New Controlled Study finds poliomavirus infection in post-mortem brains of sufferers of Autism – 67% infection with Simian Virus (SV40): ‘Vertical viral transmission represents a nongenetic mechanism of disease compatible with high parent-to-offspring transmission and with low rates of disease-specific genetic abnormalities. Vertically transmitted viruses should be found more frequently in the affected tissues of autistic individuals compared to controls. Our initial step was thus to assess by nested polymerase chain reaction (PCR) and DNA sequence analysis the presence of cytomegalovirus (CMV), Epstein-Barr virus (EBV), herpes simplex virus type 1 (HSV1), herpes simplex virus type 2 (HSV2), human herpes virus 6 (HHV6), BK virus (BKV), JC virus (JCV), and simian virus 40 (SV40) in genomic DNA extracted from postmortem temporocortical tissue (Brodmann areas 41/42) belonging to 15 autistic patients and 13 controls. BKV, JCV, and SV40 combined are significantly more frequent among autistic patients compared to controls (67% versus 23%, respectively; P <.05). The majority of positives yielded archetypal sequences, whereas six patients and two controls unveiled single–base pair changes in two or more sequenced clones.’ Laboratory of Molecular Psychiatry, Psychiatric Genetics/Neurogenetics, University Campus Bio-Medico, Rome, Italy
Note: ‘BKV, JCV, and SV40 combined are significantly more frequent among autistic patients compared to controls (67% versus 23%, respectively; P <.05′
How did Simian Virus get there, you might ask? – Inevitably, the result of vertical transmission (parent-to-child), viral shedding & inter-generational cross-contamination from Salk & Sabin Polio inoculations, sugar cube/oral drops versions & the subsequent Inactivated Polio Vaccine (or IPV) now on the schedule; permanently fixed in (altering) the germ-line DNA of successive newborns.
‘In recent years more than 60 scientific studies have found SV40 in rare human brain, bone and lung-related cancers, the same kinds of tumors the virus caused in laboratory animals. Some scientists believe SV40 may play a role in causing those cancers. One of the biggest mysteries, however, is why SV40 has been found in tumors removed from people who never received the contaminated Salk vaccine.‘
There are several possible explanations for this disturbing anomaly:
1. Direct SV40 cross-contamination from the Salk Vaccine (live Poliomavirus) co-infecting the DNA of either set of parents responsible for the baby’s genetic material now in use; passed on from mother to child via the Placenta & Colostrum (Endogenous retrovirus).
2. Direct SV40 cross-contamination of the child’s DNA (germ-line mutations) from the Salk Vaccine (live Poliomavirus), embedded in the Brain white-matter.
3. Indirect SV40 contamination from another vaccine (ie. Inactivated Polio – African Green Monkey Monkey Kidney “benign” version, Oral Polio drops – African Green Monkey Monkey Kidney “benign” version), co-infecting the DNA of either set of parents responsible for the baby’s genetic material now in use; passed on from mother to child via the Placenta & Colostrum (Endogenous retrovirus).
4. Indirect SV40 contamination from a vaccine derived from contaminated Human Diploid Cell culture (ie. Inactivated Polio, Oral Polio Drops, Hepatitis A, Measles, MMR – Rubella component) co-infecting the DNA of either set of parents responsible for the baby’s genetic material now in use; passed on from mother to child via the Placenta & Colostrum (Endogenous retrovirus).
5. Indirect SV40 contamination from a vaccine derived from contaminated Human Diploid Cell culture (ie. Inactivated Polio, Oral Polio Drops, Hepatitis A, Measles, MMR – Rubella component) co-infecting the child.
6. Indirect SV40 contamination from another Polio type vaccine (ie. Inactivated Polio – African Green Monkey Monkey Kidney “benign” version, Oral Polio drops – African Green Monkey Monkey Kidney “benign” version) co-infecting the child.
Note: Given a mother (or father) already has a compromised Immune System and/or pre-existing Medical conditions, any such infection/disorder/disease will often factor into the equation; in terms of co-infecting/altering the DNA genetic blueprint of the offspring/progeny.
‘From 1955 to 1963, the polio vaccine supplied to the United States, Canada, Europe, Asia and Africa was contaminated with SV40. Furthermore, the possibility of horizontal transmission may have enlarged this exposure. Many studies have found evidence of SV40 infection. A meta-analysis conducted by Vilchez reviewed molecular, pathological, and clinical data from 1,793 cancer patients. He concluded that there is significant data to support a role for SV40 infection in human brain cancers, bone cancers, malignant mesothelioma, and non-Hodgkin’s lymphoma.’ Cleveland College of Medicine
‘Mutations and minority variants, relative to vaccine strains, not known to affect attenuation were detected in OPV, mumps virus, and varicella-zoster virus. The anticipated detection of endogenous retroviral sequences from the producer avian and primate cells was confirmed. Avian leukosis virus (ALV), previously shown to be noninfectious for humans, was present as RNA in viral particles, while simian retrovirus (SRV) was present as genetically defective DNA.’ Journal of Virology, June 2010 vol. 84 no. 12
Note: ‘simian retrovirus (SRV) was present as genetically defective DNA.’
The multi-billion dollar Vaccine Industry has routinely been utilizing Human Diploid Cells gathered from sections of a mere two individual Fetuses. But these select babies-to-be didn’t come out of thin air…they’re not Adam & Eve either. Their individual DNA genetic blueprints, the unique germ line DNA of either Fetus was determined by each set of parents, whose own individual DNA genetic blueprint, each unique set of germ-line DNA was previously determined by their own set of parents.
This has everything to do with history. Endogenous retroviruses – remnants of ancestral exogenous retroviral infections fixed in the germ-line DNA. And remember, they were both conceived during one of the darkest chapters in Modern Medical history – that of the disastrous, misguided Salk & Sabin Polio Vaccine campaign.
There is clear distinction between the verifiable science of the body, and the detritus of propaganda supporting vaccine theory. There will indeed come a day when vaccination, vivisection, & irradiation will have gone the way of the dinosaur, replaced by non-invasive, genuinely holistic techniques; when Allopathic-type medicine, along with all the ancient tools of its trade, will crumble in the wake of an evolution of consciousness & common sense.