Do All Religious Leaders Endorse Abortion Tainted Vaccinations?

Do All Religious Leaders Endorse Abortion Tainted Vaccinations?

Devout parents who are worried about vaccines object to ingredients containing residual material from pigs or morally reprehensible DNA strands from aborted human fetuses. The New York Times published an article stating, “Top Jewish and Islamic scholars, the Vatican endorse vaccinations.” 

Religious authorities have ‘meticulously studied how vaccines are developed and what is in them,'” says the New York Times. “and still have ruled that they do not violate Jewish, Islamic or Catholic law” or Christian traditions. (source

In reality, State governments agencies target religious leaders. They are fed half-truths via packages of media materials on the topic. They are strongly encouraged to sway their parishioners to comply with state-mandated liability-free medical products that violate the body and contradict scriptures. Avoiding persecution by the state, some religious leaders ‘vigorously endorse vaccination’ and often avoid discussions with dissenting parishioners on the topic. Dodging church conflict, they parrot the public health propaganda of ‘safe and effective’ and ‘greater good’ mantra. 

What of the concerns from members who abhor abortion and reject the notion that injecting their healthy child with a disease mixed with toxins created on the body parts of aborted human beings?

Here is a recent example attempting to stem the tide of concern of millions of Christians regarding this issue author Joe Carter writes in the Gospel Coalition Article on vaccinations:

“There are currently no vaccines created by using cells directly taken from the bodies of aborted fetuses. However, there are some vaccines created from cell lines (such as WI-38, MRC-5, HEK-293, PER C6, and WI-26) that were derived from tissue taken from aborted fetuses from the 1960s.”

You could phrase what Joe Carter stated another way: Aborted baby cell strains are used in vaccine development for vaccines currently on the CDC schedule.

Updated to include: The fact is the two COVID 19 being distributed under FDA Emergency Authorization are also manufactured using the aborted fetal cell line HEK-293. Moderna in numerous patents in the fundamental design of mRNA technology and in the original vaccine research, development, production, and testing. (see references here)

Fetal Cells & Vaccines

The screen shot below is taken from the CDC Vaccine Excipient Summary. This table lists substances acknowledged by the vaccine manufacturer “as being contained in the final formulation of each vaccine.” As you can see below in the chicken pox vaccine example, MRC-5, “human diploid cells, including DNA & protein” is included in the list of ingredients.

The bottom line is that vaccine developers used cells of aborted babies to create the vaccines we use today. They were not passive actors, and according to the manufacturers themselves, certain elements from those aborted babies remain present in the vaccines. (See resources below regarding the aborted human DNA is present in vaccinations given today)

According to the CDC these vaccines developed from aborted baby cell strains are:

  • Adenovirus
  • DTaP-IPV/Hib (Pentacel)
  • DTaP-IPV (Quadracel)
  • Hep A (Havrix)
  • Hep A (Vaqta)
  • Hep A/Hep B (Twinrix)
  • MMR (MMR-II)
  • MMRV (ProQuad)
  • Rabies (Imovax)
  • Varicella (Varivax)
  • Zoster (Shingles – Zostavax).

There are no U.S. approved vaccine alternatives which were not developed via abortion for Adenovirus, Chickenpox, Hepatitis A, Measles, Mumps, or Rubella.

The cell lines from two dead babies whose parents partnered with the vaccine developers are referred to (dehumanizingly) as MRC-5 (we’ll call him Jack – he was a boy) and WI-38 (we’ll call her Jill, she was a girl). Who were they? Both were about 3 and a half months when they were tragically killed in the womb. We are told Jill’s parents had her killed because they already had too many children, and Jack’s mother had him killed for “psychiatric” reasons. Neither child was deemed to be unhealthy in any way. Here is an MMR vaccine insert which lists Jill (Wi-38) under the description.

These candidates are not selected after the abortion but are meticulously screened prior to. Dr. Stanley Plotkin who developed the Rubella vaccine by using Jill’s cells testifies:

“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 families.”

Plotkin further testified that in one study alone 76 aborted babies were similarly used in the preparatory work for a single study he participated in and that he performed medical experiments on orphans, the mentally retarded, and babies whose mothers were in prison.

Dr Peter McCullough, an Immunologist, wrote the book, The Fetus As Transplant Donor: The Scientific, Social, and Ethical Perspectives, on the methods used in harvesting fetal tissue in Sweden. He writes:

“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 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.”

Christian Leaders Claim Abortion Tainted Vaccines Morally Acceptable based on Faulty Assumptions

“The key consideration in whether using currently available vaccines is licit or immoral is whether there is material cooperation with the evil act of abortion. If the abortion was conducted in order to harvest tissues that were to be used for the vaccine, then it would clearly be immoral. But in the case of the vaccines listed above, the abortion was carried out for other reasons and the tissue was acquired post-mortem for the purpose medical research.”

Dr. McCullough and Dr. Plotkin’s testimony make it clear : It’s not like these researchers would just passively sort through discarded baby parts. They were actively involved in aborting the babies in such a way as to maximize access to “fresh” tissue. 

Catholic Religious Leaders “wash their hands of guilt” and encourage vaccination for ‘common good’

The National Catholic Bioethics Center : “Upon use, one should register a complaint with the manufacturer of the products as an acceptable form of conscientious objection,” the statement says. “This signals opposition to the wider, morally reprehensible practice of using the unborn as little more than research material for science.”

“There is no moral obligation to register such a complaint in order to use these vaccines,” it says, adding that “it should be obvious that vaccine use in these cases does not contribute directly to the practice of abortion since the reasons for having an abortion are not related to vaccine preparation.”

The above statement the Catholic leaders completely ignore the proof that abortions were performed in a manner to specifically use the innocent unborn as spare parts for the intent purpose of the research and manufacturing vaccination.  

According to the National Network for Immunization Information (NNii) the reason they used aborted babies is because “human cells are preferred because cells derived from animal organs sometimes may carry animal viruses that could harm people.”

Others, in agreement with McCullough, dispute the need for such practices to develop vaccines.

Either way, if you adopt the CDC vaccination schedule, you can’t avoid abortion tainted vaccinations.

Above is an excerpt of a 5 part series on Christians and Vaccinations that can be found at

Vaccine Exemptions Protect Religious Freedom

No, Aborted Fetal Cells were Not filtered out of the Final Vaccine:

part part 1

part 2

part 3:

part 4

A portion of the resources from website (posted her as a redundancy visit their site for the full article) 


Importantly, the new data supports NIAID’s approach to a gene-based vaccine for COVID-19 and will also be useful in other vaccine approaches including protein-based vaccines and other nucleic acid or vector-based delivery approaches. NIAID scientists designed the stabilized spike antigen based on previous knowledge obtained from studying other coronavirus spike structures. NIAID and the biotechnology company Moderna, based in Cambridge, Massachusetts, are developing a messenger RNA (mRNA) vaccine, which directs the body’s cells to express the spike in its prefusion conformation to elicit an immune response.

And the Materials and Methods show the 293 cells.

And if that is not enough, Moderna’s use of HEK is not new…previous patents in 2015 show its use as well.  Use the Find function and type in HEK in the search…it’s listed 76 times.,999,380.PN.&OS=PN/8,999,380&RS=PN/8,999,380

Also – more here showing how HEK-293 cells are used with the Spike S protein:

Now, if you still need convincing that Moderna is using HEK-293 cells, this  is straight from their own website:

And from their Publications page, see this link:

Since it deals with lung infection (which Covid-19 causes) it seems like a pretty good reference to what they are doing.  The use of 293 cells is cited in several places including in the supplementary information.  That is linked here:

The very first paragraph shows the use of 293 cells IN THE CONSTRUCTION. The authors of the study are both Merck and Moderna.

And in July 2020: An mRNA Vaccine against SARS-CoV-2 — Preliminary Report


Which clearly states they are using the Spike protein which some have tried to deny.

Under  Vaccine – Quoting:

The mRNA-1273 vaccine candidate, manufactured by Moderna, encodes the S-2P antigen, consisting of the SARS-CoV-2 glycoprotein with a transmembrane anchor and an intact S1–S2 cleavage site. S-2P is stabilized in its prefusion conformation by two consecutive proline substitutions at amino acid positions 986 and 987, at the top of the central helix in the S2 subunit.8

And voila – Reference no. 8 at the bottom of the page is none other than:

Wrapp D, Wang N, Corbett KS, et al. Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation. Science 2020;367:1260-1263.

In addition, both the Protocol

and Supplemental Information  linked at the bottom of the NEJM article show the use of HEK-293.

Also the article dated August 2020, clearly shows the use of the HEK293 as well for the mRNA-1273 vaccine.

Just a sampling –  page 9 of the Nature article:

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