Pfizer–BioNTech COVID 19 vaccine Puns

As per https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251011/
Also, there is also this additional "small" issue related to PEG injections - https://pubmed.ncbi.nlm.nih.gov/31526095/

On the other hand, Inovio's vaccines consist only of water and DNA plasmids, no preservatives no adjuvants nothing else. This is one of the reasons the vaccine safety profile is great.

As a side note, just a thought...Since PEG is fundamental to the mRNA vaccine delivery method and since our immune system can be sensitized to PEG if it is exposed to it multiple times. Is it possible that because they are injecting billions of people with this stuff, including children, they can effectively sensitize a huge amount of people to PEG? This would be quite unfortunate for the other therapies in their pipelines since they would not be able to deliver them with the same method because of the potential allergic reactions and inventing a new delivery method for the fragile mRNA molecule is far from trivial.

Vaccines and Related Biological Products Advisory Committee Meeting October 26, 2021 FDA Briefing Document EUA amendment request for Pfizer-BioNTech COVID-19 Vaccine for use in children 5 through 11 years of age p 14:

>To provide a vaccine with an improved stability profile, the Pfizer-BioNTech COVID-19 Vaccine for use in children 5-11 years of age uses tromethamine (Tris) buffer instead of the phosphate- buffered saline (PBS) as used in the previous formulation

Tris buffer is used in gene therapy experiments, for example:

Rapid and simplified purification of recombinant adeno-associated virus

>Preclinical gene therapy studies both in-vitro and in-vivo require high purity preparations of adeno-associated virus (AAV).
>
>Tris buffer had to be excluded from the buffer solution as even small traces of Tris can be highly toxic in in vivo experiments.

EMA Assessment report Comirnaty Common name: COVID-19 mRNA vaccine (nucleoside-modified) p. 21

>Residual DNA template is a process-related impurity derived from the linearised DNA template added to the in-vitro transcription reaction. Residual DNA template is measured as defined in the active substance specification. The levels are controlled by a specification limit which is considered suitably low.

p: 17:

>The robustness of the DNase digestion step is not considered comprehensively demonstrated although there is routine control of residual DNA impurities at the active substance level. It has been confirmed that studies to enhance the robustness of this step are ongoing and these should be reported (REC7).

The TGA knows the spike protein from the Pfizer/BioNTech COVID-19 vaccine enters the nucleus.

So... was it intended to go to the nucleus all along? Lipid nanoparticles are not only "protecting the mRNA from degradation" but are a transfectant facilitating nuclear delivery.

Is spike protein causing catastrophic damage to DNA?

There are also concerns with the effects the COVID-19 "vaccines" have on the children's immune systems:

['The BNT162b2 mRNA vaccine again

The government of Vietnam said Sunday it has approved the COVID-19 vaccine jointly made by Pfizer and BioNTech for domestic emergency use.

Jesse Santiano M.D.Don't Get Sick!Know the Absolute Risk Reduction of the COVID-19 Vaccines! Part 1 (drjessesantiano.com)

The government of Vietnam said Sunday it has approved the COVID-19 vaccine jointly made by Pfizer and BioNTech for domestic emergency use.