CMDA's The Point

Ethical Science at Warp Speed

November 16, 2020
Oil Bubbles July 31, 2018

by David Prentice, PhD

COVID-19 has brought many challenges to us all—medical, ethical, societal. It has also intensified and sharpened the focus of some ongoing bioethical challenges, especially regarding fetal tissue research and the related topic of abortion-derived cell lines and vaccine production. We looked at both of these issues in the spring of 2020, early in the COVID-19 pandemic. Time for some updates, new information and analysis.

In March, we looked at the continuing controversy of fetal tissue research, especially with regard to the science and federal taxpayer funding of research with fetal tissue from ongoing abortion. Pro-abortion advocates including some scientists continue to claim that fetal tissue research saves lives and is vital to medical research, yet those claims for fetal tissue are specious and have been repeatedly proven false. The efforts to promote use of fetal tissue from induced abortion undermine research and funding that can actually help COVID-19 patients, including development of drugs as well as the potential use of adult stem cells to treat severe cases of COVID-19.

Ethical review of fetal tissue research and its funding has moved ahead as well. A peer-reviewed, comprehensive review paper on fetal tissue science, ethics and policy published in August 2020 goes into great detail on these various aspects of human fetal tissue research, debunking the claims and highlighting the numerous alternatives.

On the policy front, both the U.S. Senate and the House of Representatives called for an end to funding for human fetal tissue research, and the call to end unethical research and instead support successful, ethical science was echoed in a letter by 19 Attorneys General.

As discussed previously, the Trump administration in June 2019 stopped federal taxpayer funding of human fetal tissue research at government laboratories (“intramural research”), shifted federal funds toward development of ethical alternative research methods, and instituted an ethics review for extramural grant proposals seeking funding for further fetal tissue research. The ethics review requirement was placed into statute in 1993, but this was the first time any presidential administration invoked the ethics review. The statute spells out the procedures and makeup of the Ethics Board, including the definition: “the term ‘ethical considerations’ means considerations as to whether the nature of the research involved is such that it is unethical to conduct or support the research.” As discussed previously, nominations for the Ethics Board were solicited in February 2020. After subsequent selection of the 15 members, a meeting of the Human Fetal Tissue Research Ethics Advisory Board was scheduled for July 31, 2020.

The Human Fetal Tissue Ethics Advisory Board meeting included an open public session, welcome and charge to the board members, brief introductions of the 15 highly-credentialed professionals selected to serve, explanations of confidentiality and meeting procedures, and comments from the public. The board then went into closed session for more than five hours to discuss grant proposals requesting funds for use of human fetal tissue. Of the 14 proposals considered by the Ethics Advisory Board, only one was recommended for funding. The public report gives more details about the reviews (while maintaining confidentiality standards.) An interesting sidelight were complaints by some, including two board members, that the makeup of the panel was “stacked” against human fetal tissue research because of the supposed inclusion of numerous members opposed to abortion or fetal tissue research, and that the rejections were a foregone conclusion. Yet the actual votes shown in the public report tell a different story, with more than one-third of the proposals rejected by unanimous (15-0) or near-unanimous (14-1) votes; apparently even many of those favoring fetal tissue research could not in honesty see many of the proposals as ethical. As far as the board’s makeup, a published analysis shows that this was the first federal bioethics panel in over 40 years with a relatively balanced makeup. There are still a large number of federally-funded fetal tissue research grants, but the hope is that the movement to modern, ethical techniques will accelerate. Indications are that more scientists are moving away from use of fetal tissue from induced abortion, and that NIH is encouraging scientists to remove fetal tissue from proposals.

Vaccine development against COVID-19 also shows movement away from use of old, ethically controversial methods and cell sources to modern, ethically-sourced techniques. As we had discussed earlier in the year, the ethical consideration in this case has nothing to do with fetal tissue and ongoing abortion, but rather with the questionable ethics of using abortion-derived cell lines in vaccine production. Cells are needed for growth of viruses, since viruses are not free-living organisms, but rather must live and grow inside cells, hijacking cellular machinery for viral reproduction. Most current FDA-approved viral vaccines are made by growing the virus in cells, breaking open the cells to harvest large quantities of virus and then inactivating or weakening (“attenuating”) the virus. The whole virus is then injected as the vaccine, and our immune system reacts to this foreign object and prepares antibodies and cellular defenses against any future infection. The vast majority of cell sources for approved viral vaccines are ethically derived: various types of animal cells, insect cells, yeast, chicken eggs. But a few approved viral vaccines (nine out of 58) still are produced using one of two fetal cell lines (WI-38, MRC-5) from an abortion decades ago. Two other abortion-derived cell lines (HEK293, PER.C6) are used to make genetically-engineered adenoviruses or other viruses, or to make large quantities of protein. Cell lines are derived by growing cells in the laboratory; some cell lines have a limited life span, while other cell lines have become immortalized, capable of continuing to grow indefinitely in the lab. Fetal cell lines are in no way fetal tissue; there is a great separation both in time and in space from the original body tissue. But there remains an ethical lineage that can be traced back to the original abortion that destroyed a young human life, and that terrible origin is what causes conscience concerns among many people.

At last count, there were over 200 COVID-19 vaccine candidates; at least 39 of these are in clinical trials, though none of these have yet passed through all phases of clinical testing. So do any of the COVID-19 vaccines being developed use abortion-derived cell lines in their production? Sadly, some do, but most do not. This is due in part to several new vaccine development techniques being used. The newer techniques don’t grow whole virus for a vaccine. Instead, they use molecular techniques to create just a part of the virus, and they show that recognizable part to our immune system. (We’ve created a visual primer to show each of these techniques as well as the traditional method.) One technique makes a “viral vector,” essentially a carrier virus that transports the genetic instructions to make the viral spike protein into our cells, where the genetic information is used to make the actual protein. Another technique makes the viral protein in laboratory-grown cells, then injects the protein itself (sometimes with an adjuvant, a chemical that increases immune response) as the vaccine. Another new vaccine production technique creates mRNA in the laboratory without use of any cells, just using enzymes in a test tube; mRNA is a genetic instruction or recipe that tells how to make a protein. The mRNA recipe is encased in a lipid particle (like an oil droplet), and that is what is injected as the vaccine. The mRNA goes into our cells, and the genetic recipe is read and spike protein is made in our cells, to show to our immune system. One other new method is similar, making a DNA information molecule in the laboratory without using any cells. This genetic recipe is then given to a cell, and the information is read and used to produce the protein in our cells for our immune system.

As noted, most of the COVID-19 vaccines under development do not use an abortion-derived cell line in their development or production. This includes most of the Warp Speed candidates.[i] The rapidity of vaccine development in these cases comes not from cutting corners, but from use of the faster, modern molecular techniques for vaccine creation, as well as overlapping various parts of the normally-linear process of vaccine development, production and clinical trials. Warp Speed funding has been used to scale up production, do clinical trials and order doses of vaccines, even before knowing whether a particular vaccine will work and freeing vaccine developers to move more swiftly. All vaccines produced still must be proven safe, and they must meet a minimum effectiveness (at least 50 percent effective.)

Regarding conscience questions, knowing a vaccine’s lineage and how it is produced is essential in making an informed decision. The possibility for conscience concerns by potential vaccine recipients also creates ethical demands on policymakers, healthcare officials, scientists, vaccine creators and funders, whether or not they themselves have an ethical concern. Access to a safe, effective vaccine by the entire citizenry is a public health issue. This is why it is important to advocate for vaccines produced using ethical methods. We should also advocate for new, ethically-sourced cells and methods used in quality-control tests of vaccines. Production method directly affects the vaccine recipient, it determines what is injected, and ethical production lines are important in conscience considerations. Testing methods bear on the ethical choices of the scientists, and we should consider their consciences as well.

We have produced a chart, updated as possible, that gives background information on a number of the COVID-19 vaccines, including any use of abortion-derived cell lines, to help people make informed choices.


[i]  The chart found here on the Charlotte Lozier Institute website details additional COVID vaccine candidates, including Operation Warp Speed candidates that used fetal cells from the HEK-293T cell line to perform a confirmatory lab test.

David Prentice, PhD

About David Prentice, PhD

David A. Prentice is Vice President and Research Director for the Charlotte Lozier Institute. He is also Adjunct Professor of Molecular Genetics at the John Paul II Institute, The Catholic University of America and was a Founding Advisory Board Member for the Midwest Stem Cell Therapy Center, a unique comprehensive stem cell center in Kansas that he was instrumental in creating. In 2020, he was appointed by the Secretary of HHS to the federal Human Fetal Tissue Ethics Advisory Board. Dr. Prentice has over 40 years’ experience as a scientific researcher and professor, including previous service as senior fellow for life sciences at the Family Research Council, Professor of Life Sciences at Indiana State University, and Adjunct Professor of Medical and Molecular Genetics, Indiana University School of Medicine. He established Stem Cell Research Facts, an educational website providing scientific facts and patient-centered videos about adult stem cells, and is a founding member of Do No Harm: The Coalition of Americans for Research Ethics, and an advisory board member for the Center for Bioethics and Human Dignity. He has provided scientific advice for numerous medical professionals, legislators, policymakers and organizations at the state, federal, and international levels. Dr. Prentice received his Ph.D. in biochemistry from the University of Kansas, and was at Los Alamos National Laboratory and the University of Texas Medical School-Houston before joining Indiana State University where in addition to his research and teaching, he served as Acting Associate Dean of Arts and Sciences and Assistant Chair of Life Sciences. He was recognized with the University’s Caleb Mills Distinguished Teaching Award and Faculty Distinguished Service Award. He has taught courses ranging from non-majors biology to advanced and graduate courses including developmental biology, embryology, cell and tissue culture, history of biology, science and politics, pathophysiology, medical genetics, and medical biochemistry. Several of his courses were also taught on-line. He received the 2007 Walter C. Randall Award in Biomedical Ethics from the American Physiological Society, given for promoting the honor and integrity of biomedical science through example and mentoring in the classroom and laboratory. Dr. Prentice’s research interests encompass various aspects of cell growth control, cell and developmental biology; one major focus is adult stem cells. He has reviewed for various professional publications including The Journal of the American Medical Association. He is an internationally-recognized expert on stem cell research, cell biology and bioethics, and has provided scientific lectures and policy briefings in 40 states and 21 countries, including testimony before the U.S. Congress and numerous state legislatures, the U.S. National Academy of Sciences, the President’s Council on Bioethics, European Parliament, British Parliament, Canadian Parliament, Australian Parliament, German Bundestag, French Senate, Swedish Parliament, the United Nations, and the Vatican. He was selected by President George W. Bush’s U.S. President’s Council on Bioethics to write the comprehensive review of adult stem cell research for the Council’s 2004 publication “Monitoring Stem Cell Research.” Dr. Prentice has published numerous scientific and bioethics articles, including a recent review of stem cell science and adult stem cell treatments published in Circulation Research. He has also published numerous commentaries and op-eds, and travels nationally and internationally to give frequent invited lectures regarding stem cell research, fetal tissue research, gene editing, cloning, embryology, cell culture and vaccines, bioethics, and public policy. He has been interviewed in virtually all major electronic and print media outlets, including CNN, ABC, NBC, CBS, Fox, CSPAN, Reuters, AP, NPR, USA Today, BBC, The Washington Post, The Los Angeles Times, and The New York Times.

3 Comments

  1. Avatar Guy Schultz on November 20, 2020 at 10:04 am

    Confirmatory testing with cells derived from the aborted baby still represents an abuse of the sanctity of that child. Without that killing, the cell line does not exist. Why is it so hard to admit that it is wrong yet we still use it? Isn’t it further sin to seek to justify or explain away this for expedience?

    Take the use of the cell line in the PepsiCo case where lifenews and the children of God along with other prolife groups called for a boycott . The outrage at the sec ruling under the Obama administration, the it was ordinary business. That would be using that cell line in similar context (testing flavors by creating taste sensors from the cells). The produce did not contain the fetal matter, but was benefited by their use. We can condemn that at give the Trump administration a pass on the Moderna use for confirmatory testing. Dishonest weights are detestable to the Lord.



  2. Avatar C.Philip Hudson MD FAAFP on December 6, 2020 at 11:34 pm

    I must say the “Visual Primer…” referenced in this article is excellent ,concise resource. It definitely cleared up my understanding of the general types of vaccines being developed, but clearly describes how this virus attacks us at a cellular level.
    I have sent it out to my email friends to better educate them.



  3. Avatar Phyllis Mills on December 10, 2020 at 11:50 am

    There are some articles out there that state that the vaccine will become mandatory and there will be a way to determine if a person has, indeed, had the vaccine. Currently Bill Gates and his wife have applied for a patend called Luciferace 060606 that would enable such tracking. How does a person find out if this will become a fact? I think you see where I am going here. The Mark of the Beast is numbered 666 and everyone that wants to live in the world, shop and travel must have the Mark.