mRNA Vaccines; DNA Will Be Hit!

2021 John A. Catanzaro

Translate, please! On many occasions, while in Mexico, I put together and associate words in English; however, sometimes, the English word equivalent was not sufficient to describe the Spanish word’s full meaning.

As we continue to observe emerging problems with the increasing bad reactions to the current Pfizer and Moderna mRNA vaccines, two words can describe such reactions, random and unpredictable.

Just as saying the wrong word at the wrong time can be often embarrassing and potentially damaging because of the inadequate understanding of the spoken language, so can mRNA misdirected translation be toxic and unpredictable.

The current mRNA vaccine designs alter the inherent quality control mechanisms of the human cell and systems. Aberrant, misfolded, and mislocalized proteins are often toxic to human cells and can result in many human diseases. Vaccinated individuals experience a perplexing degree of symptoms that mimic disease, and many have died from poisonous reactions.

“Translation” is a keyword here. Several distinct mechanisms control the quality of mRNA and proteins during the translation process. mRNA quality control systems include nonsense-mediated decay (NMD), non-stop decay (NSD), and no-go decay (NGD). Failure of an intact quality system will result in random rogue reactions resulting in severe downstream consequences. All proteins of the human body are subject to these quality control mechanisms. This quality mRNA control system influences what is collectively known as the protein to protein interaction (PPI) system. A single misplaced failure can virtually affect downstream proteins responsible for controlling and maintaining human body systems.

The current mRNA vaccine design used a segment of viral-related mRNA with the hope of producing an immune response using a viral mimicry mechanism that makes random fragment protein segments with the action of eliciting an immune response. This technology is new and not fully understood.

Genetic information during transcription and translation into correctly folded active proteins localized at the proper places for their functioning is a normal process of maintaining quality control. Despite high fidelity quality control mechanisms, defective proteins can result from mutations, mistakes in transcription, stress, or other reasons. This phenomenon may explain the basis of the varied adverse severe reactions and death related to the mRNA vaccine design. People should not be deceived DNA will be hit!

“Jumping Genes” This is how DNA can be hit:

The L1 encode an endonuclease and a reverse transcriptase to perform Retrotransposition by which they propagate their own sequence within the human genome.

Simplified, Retrotransposition means that the L1-encoded mRNA gets translated into the endonuclease and reverse transcriptase in the cytosol.

These proteins have a high affinity to bind their own encoding mRNA and can re-enter the nucleus, where the endonuclease cuts the genomic DNA at a specific target sequence and the L1-mRNA gets Reverse transcribed into DNA which gets integrated into the genome.

Boom, you have a new L1 copy in the genome.

However, the L1 encoded proteins are not 100% precise in detecting their “own” sequence and therefore sometimes Retrotranspose other sequences they encounter in the cytosol instead.

Both Pfizer and Moderna engaged in a very young technology with unproven safety in humans with serious consequences. Johnson and Johnson’s vaccine is also seriously flawed causing reactions that include bleeding disorder and clotting resulting in death. The same is to be said for AstraZeneca.

People that are vaccinated are experiencing significant, unpredictable reactions to the first injection with increasing severity of responses with the second injection. These vaccine reactions are more troublesome than the disease. Doctors cannot implement adequate life-saving measures due to the myriad unpredictable cascading adverse responses resulting from the vaccine.

Over 50,000 serious adverse reactions are reported, with a climbing 5,000 related deaths. mRNA Vaccine-associated deaths will continue to climb, and we will observe mRNA vaccine-induced injuries escalate over the next several months to years worse than the virus.

Herd Immunity Not Possible With Existing Vaccines!

The globe continues to experience a rising number of people infected with the virus despite mass vaccination. New variants continue to be a threat as a consequence of an increasing infection and vaccination rate.

Current vaccines do not prevent transmission or stop the spread of the virus. Current mRNA designs do not offer any lasting protections and maybe consequently creating more complex viral sequela.

The most effective way to achieve viral eradication is with a CD8 T Cell defense treatment design. COVID will continue to rise with more complicated mutations, and herd immunity not possible. It will be no different than chasing the proverbial annual influenza. Only worse as the roque proteins resulting from the existing vaccines fuel the viral fire!

Reference:

John A. Catanzaro is CEO of Neo7logix, a bioscience company that designs precision and personalized treatment designs. www.neo7logix.com

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