Pfizer’s mRNA vaccine against COVID is now being marketed under …

Comment on Dr. Peter McCullough’s COVID-19 and Anti-Vaccine Theories by Sean Pitman.

Pfizer’s mRNA vaccine against COVID is now being marketed under the name “Comirnaty” following FDA approval (Link). This isn’t a different vaccine. It’s the very same vaccine.

“The FDA-approved Pfizer-BioNTech product Comirnaty (COVID-19 Vaccine, mRNA) and the FDA-authorized Pfizer-BioNTech COVID-19 Vaccine under EUA have the same formulation and can be used interchangeably to provide the COVID-19 vaccination series without presenting any safety or effectiveness concerns. Therefore, providers can use doses distributed under EUA to administer the vaccination series as if the doses were the licensed vaccine. For purposes of administration, doses distributed under the EUA are interchangeable with the licensed doses.”

As far as liability is concerned, again, liability has been taken over by the government so that the vaccines can be made avaiable to everyone. Otherwise, only the rich would be able to afford vaccines.

Sure, this is the first time that mRNA technology has been used to produce a vaccine for the general public. However, it is not the first time that the mRNA technology itself has been successfully used.

Patisiran is based on the very same mRNA technology used in the Pfizer and Moderna vaccines. It uses lipid nanoparticles to deliver specially coded mRNA into human cells to produce the desire protein sequences to treat disease. About 1,000 people have been using Pitisiran since 2017. Now, the mRNA vaccines against COVID-19 use two injects of 30μg (Pfizer) to 100μg (Moderna) of mRNA for each injection. In comparison, Patisiran uses around 100x this dose of mRNA, which gets injected intravenously every three months . . . indefinitely since 2017. And, this was done with good safety as well as efficacy results (Link).

So, it isn’t the mRNA technology that is a potential problem. This technology is demonstrably very safe and very effective indeed. The only real question, then, is in regard to the protein product of the vaccine – the “spike protein” in the case of the mRNA vaccines against COVID-19. That’s really the only question here. And, the mRNA vaccines, producing the modified spike protein of COVID-19, have been extensively tested via large double-blinded placebo-controlled trials in both humans and animals – with amazing success regarding efficacy as well as safety. And, these results have continued on now that hundreds of millions of vaccines have been given worldwide. The fact of the matter is that hospital ICUs are currently filling up with those who are very sick and who are dying with COVID-19 (the Delta Variant right now). The significant majority of these people are unvaccinated. These ICUs are not filling up with the vaccinated at all. The vaccines are very clearly highly protective against serious COVID-19 infections. That’s the very clear weight of evidence that we have in hand.

Sean Pitman Also Commented

Dr. Peter McCullough’s COVID-19 and Anti-Vaccine Theories
Fetal cell lines, originally produced decades ago, were used in the testing of the mRNA vaccines – as they were in the testing of Tylenol, Motrin, Robitussin, Aspirin, Sudafed, Tums, Lidocaine, and a host of other modern medications that most people use on a semiregular basis (Link).

Dr. Peter McCullough’s COVID-19 and Anti-Vaccine Theories
I see no evidence that the published ingredient lists for the mRNA vaccines are not transparent and factual. There just is no credible evidence for “graphene” in these vaccines and fetal cell lines simply aren’t necessary to produce these types of vaccines.

Dr. Peter McCullough’s COVID-19 and Anti-Vaccine Theories
The hospitalization/death rate is far less for the vaccinated vs. the unvaccinated (Link). Note, in this line, that those states with the lowest vaccination rates have the highest death rates per capita:

As far as natural immunity gain via a prior COVID-19 infection, it can actually be superior to the immunity gained via full vaccination. However, natural immunity is less predictable. Up to a third of people who were previously infected by COVID-19 don’t develop antibodies against it (Link). However, if one can demonstrate an adequate level of antibodies against COVID-19 it seems reasonable to me that such people should be considered to have adequate immunity.

As far as the immunity generated by vaccination, the type of immunity generated would not be so effective at preventing a mucosal nasopharyngeal infection since the types of antibodies produced (IgG and IgM) would preferentially be blood-based rather than tissue-based (IgA) type of immunity (Link). Because of this, naturally derived immunity might have an additional advantage in this regard as well.

Recent Comments by Sean Pitman

Mandates vs. Religious Exemptions
That’s true. So, the question is if these limitations are substantial enough to reasonably overcome the conclusions of the authors. The fact remains that your own personal experience doesn’t seem to be the same as those published in papers like this one where there are actual reinfections for those who have previously had COVID-19. Several friends of mine have been reinfected and a cousin of mine has been reinfected three times…

Mandates vs. Religious Exemptions

Mandates vs. Religious Exemptions
There’s “peer review” and then there’s peer review.

Beall remained critical of MDPI after removing the publisher from his list of predatory open access publishing companies. In December 2015 he wrote that, “It is clear that MDPI sees peer review as merely a perfunctory step that publishers have to endure before publishing papers and accepting money from the authors” and that “it’s clear that MDPI’s peer review is managed by clueless clerical staff in China.”

Beall, Jeffrey (17 December 2015). “Instead of a Peer Review, Reviewer Sends Warning to Authors”. Scholarly Open Access. Archived from the original on 13 March 2016.

In July 2021, an article titled “Journal citation reports and the definition of a predatory journal: The case of the Multidisciplinary Digital Publishing Institute (MDPI)” was published in the academic journal Research Evaluation, written by María Ángeles Oviedo-García. Oviedo-García argued that MDPI used self-citation practices known as “citation cartels” to increase the apparent Impact Factor of MDPI journals, and that MDPI journals bear a number of hallmarks of predatory publishing. MDPI also released a public comment on the article on August 19th, 2021, claiming the article was predicated on the notion that MDPI was a predatory publisher, and that the article misrepresents MDPI business practice. In that comment, MDPI did confirm that its journals had some of the highest self-citation rates amongst academic publishers. The article in Research Evaluation later received an editorial “Expression of Concern,” and as of November 25th 2021, an investigation is ongoing.

Regardless of all of this, the main point that the authors of this paper make is not substantiated by their research. T-cells and B-cells simply are not affected by the mRNA vaccines to any significant degree. So, their arguments really are mute here. That’s the bottom line. You still have no mechanism behind your claims that the mRNA vaccines are more dangerous than they are beneficial or more risky than getting a live COVID-19 infection.

Mandates vs. Religious Exemptions
Don’t you also disagree, by definition, with anything that doesn’t agree with your views? Come on now. If I agreed, then there would be no disagreement. The real question is, who has the greater weight of evidence? Again, where is your evidence? Where is your mechanism that makes any sense?

Mandates vs. Religious Exemptions
The spike protein that is produced by the mRNA vaccines has an anchoring portion, a “transmembrane domain” that keeps it embedded in the membrane of the muscle cell that produced it.

“The end product in host cells expressing these mRNA vaccines is a surface-exposed, membrane-anchored, glycosylated, and trimerized Spike protein resembling the 3-D structure of the native viral Spike protein, to the extent that it interacts with its cognate receptor, hACE2.” (Link)